Year |
Citation |
Score |
2012 |
Paquette LA, Ross RJ, Springer JP. Stereocontrolled construction of an ingenol prototype having a complete array of oxygenated and unsaturated centers. Journal of the American Chemical Society. 110: 6192-204. PMID 22148799 DOI: 10.1021/Ja00226A039 |
0.505 |
|
2010 |
Paquette LA. Silicon-mediated organic synthesis. Science (New York, N.Y.). 217: 793-800. PMID 17778295 DOI: 10.1126/Science.217.4562.793 |
0.301 |
|
2010 |
Pettigrew JD, Paquette LA. Efforts toward the synthesis of pseudolaric acid a: Intramolecular bromoetherification as a multipurpose synthetic tool Heterocycles. 80: 99-102. DOI: 10.3987/Com-09-S(S)7 |
0.359 |
|
2010 |
Hartung R, Paquette L. ChemInform Abstract: New Synthetic Tactics Designed to Access Diynes and Polyynes Cheminform. 33: no-no. DOI: 10.1002/chin.200251241 |
0.751 |
|
2010 |
Paquette LA, Owen DR, Bibart RT, Seekamp CK, Kahane AL, Lanter JC, Alvarez Corral M. ChemInform Abstract: 1-Oxaspiro[4.4]nonan-6-ones. Synthetic Access via Oxonium Ion Technology, Optical Resolution, and Conversion into Enantiopure Spirocyclic α,β-Butenolides. Cheminform. 32: no-no. DOI: 10.1002/chin.200136107 |
0.761 |
|
2010 |
MITZEL TM, PAQUETTE LA. ChemInform Abstract: Linear and Cyclic Carbon Systems. Cheminform. 28: no-no. DOI: 10.1002/chin.199725282 |
0.729 |
|
2010 |
PAQUETTE LA, HORMUTH S, LOVELY CJ. ChemInform Abstract: Studies Directed Toward the Total Synthesis of Cerorubenic Acid-III. Part 4. Exploration of an Organometallic Approach to Construction of the Eastern Sector. Cheminform. 26: no-no. DOI: 10.1002/chin.199549227 |
0.579 |
|
2010 |
PAQUETTE LA, COMBRINK KD, ELMORE SW, ROGERS RD. ChemInform Abstract: Impact of Substituent Modifications on the Atropselectivity Characteristics of an Anionic Oxy-Cope Ring Expansion. Cheminform. 22: no-no. DOI: 10.1002/chin.199126107 |
0.681 |
|
2009 |
Wang X, Butler SC, Gallucci JC, Paquette LA. Enolization regioselectivity involving stereoisomeric 4a-methyl-5-methoxyperhydrobenzo[7]annulen-2-ones. The Journal of Organic Chemistry. 74: 6825-30. PMID 19642628 DOI: 10.1021/Jo901391D |
0.367 |
|
2009 |
Paquette LA, Dura RD, Modolo I. Contrasting responses of pyrido[2,1-a]isoindol-6-ones and their sultam counterparts to photochemical activation. The Journal of Organic Chemistry. 74: 1982-7. PMID 19199670 DOI: 10.1021/Jo802476C |
0.375 |
|
2009 |
Paquette LA, Moura-Letts G, Wang GP. From D-glucose to enantiomerically pure cycloctanoses. The glycosidase inhibitory capacity of medium-ring carbasugars. The Journal of Organic Chemistry. 74: 2099-107. PMID 19173597 DOI: 10.1021/Jo802620H |
0.321 |
|
2009 |
Proust N, Preston AJ, Paquette LA. Workable synthetic routes to functionalized 1,6-benzodiazocines Heterocycles. 77: 163-166. DOI: 10.3987/Com-08-S(F)10 |
0.329 |
|
2009 |
Paquette LA, Lai KW. Claisen ring expansion approach toward the CDEF ring system of lancifodilactone G Heterocycles. 79: 299-302. DOI: 10.3987/Com-08-S(D)2 |
0.353 |
|
2009 |
Braun A, Cho IH, Ciblat S, Clyne D, Forgione P, Hart AC, Huang G, Kim J, Modolo I, Paquette LA, Peng X, Pichlmair S, Stewart CA, Wang J, Zuev D. Enantioselective synthesis of structurally intricate and complementary polyoxygenated building blocks of spongistatin 1 (altohyrtin a) Collection of Czechoslovak Chemical Communications. 74: 651-769. DOI: 10.1135/Cccc2008181 |
0.819 |
|
2008 |
Gallucci JC, Dura RD, Paquette LA. 7-Bromo-4b-methyl-7,8-dihydro-4bH-9-thia-8a-aza-fluorene 9,9-dioxide. Acta Crystallographica. Section E, Structure Reports Online. 64: o1303. PMID 21202932 DOI: 10.1107/S1600536808017972 |
0.372 |
|
2008 |
Moura-Letts G, Paquette LA. Contiguously substituted cyclooctane polyols. configurational assignments via (1)H NMR correlations and symmetry considerations. The Journal of Organic Chemistry. 73: 7663-70. PMID 18761439 DOI: 10.1021/Jo801443D |
0.336 |
|
2008 |
Paquette LA, Wah Lai K. Pinacol macrocyclization-based route to the polyfused medium-sized CDE ring system of lancifodilactone G. Organic Letters. 10: 3781-4. PMID 18683932 DOI: 10.1021/Ol8014607 |
0.315 |
|
2008 |
Proust N, Gallucci JC, Paquette LA. Neighboring group participation by sulfonamido nitrogen. The Journal of Organic Chemistry. 73: 6279-82. PMID 18630964 DOI: 10.1021/Jo800952M |
0.306 |
|
2008 |
Paquette LA, Peng X, Yang J, Kang HJ. The carbohydrate-sesquiterpene interface. directed synthetic routes to both (+)- and (-)-fomannosin from D-glucose. The Journal of Organic Chemistry. 73: 4548-58. PMID 18489155 DOI: 10.1021/Jo8004233 |
0.682 |
|
2008 |
Lai KW, Paquette LA. Stereocontrolled synthesis of the sterically encumbered F ring of lancifodilactone G. Organic Letters. 10: 2115-8. PMID 18454538 DOI: 10.1021/Ol800419V |
0.333 |
|
2008 |
Paquette LA, Lai KW. Studies directed toward the total synthesis of lancifodilactone G: an expeditious route to the ABC subunit. Organic Letters. 10: 2111-3. PMID 18454534 DOI: 10.1021/Ol800418M |
0.357 |
|
2008 |
Paquette LA, Dura RD, Gallucci JC. Photodimerization of pyrido[2,1-a]isoindol-6(4H)-one Heterocycles. 76: 129-132. DOI: 10.3987/Com-07-S(N)2 |
0.32 |
|
2008 |
Stewart CA, Peng X, Paquette LA. An efficient means for generating p-methoxybenzyl (PMB) ethers under mildly acidic conditions Synthesis. 0433-0437. DOI: 10.1055/S-2008-1032132 |
0.469 |
|
2007 |
Gallucci JC, Inomata K, Dura RD, Paquette LA. (+)-(1S,5R,10S)-11,11-Dimeth-yl-4-oxa-tricyclo-[8.4.0.0]tetra-deca-ne-3,12-dione. Acta Crystallographica. Section E, Structure Reports Online. 64: o287. PMID 21200853 DOI: 10.1107/S1600536807066159 |
0.348 |
|
2007 |
Hilmey DG, Davis BD, Gallucci JC, Brodbelt JS, Paquette LA. X-ray crystallographic and mass spectrometric probing of the conformational and ionophoric properties of stereoisomeric hexatetrahydrofuranylhexane segments. The Journal of Organic Chemistry. 72: 9088-101. PMID 17958448 DOI: 10.1021/Jo7016229 |
0.313 |
|
2007 |
Paquette LA, Peng X, Yang J. Asymmetric synthesis of the phytopathogen (+)-fomannosin. Angewandte Chemie (International Ed. in English). 46: 7817-9. PMID 17823900 DOI: 10.1002/Anie.200702056 |
0.626 |
|
2007 |
Adaligil E, Davis BD, Hilmey DG, Shen Y, Spruell JM, Brodbelt JS, Houk KN, Paquette LA. Synthesis of, and structural assignments to the stereoisomers of bis (2,2')- and tris (2,2',2")-tetrahydrofurans: conformational features and ionic binding capacities of these gateway polycyclic networks. The Journal of Organic Chemistry. 72: 6215-23. PMID 17629342 DOI: 10.1021/Jo0708238 |
0.326 |
|
2007 |
Ciblat S, Kim J, Stewart CA, Wang J, Forgione P, Clyne D, Paquette LA. A modular approach to marine macrolide construction. 4. Assembly of C36-C51 and C29-C44 building blocks and evaluation of key coupling reactions targeting spongistatin 1 (altohyrtin A). Organic Letters. 9: 719-22. PMID 17286379 DOI: 10.1021/Ol063083I |
0.703 |
|
2007 |
O'Connor PD, Knight CK, Friedrich D, Peng X, Paquette LA. Pectenotoxin-2 synthetic studies. 3. Assessment of the capacity for stereocontrolled cyclization to form the entire C1-C26 subunit based upon the double bond geometry across C15-C16. The Journal of Organic Chemistry. 72: 1747-54. PMID 17269830 DOI: 10.1021/Jo062513F |
0.574 |
|
2007 |
Bedore MW, Chang SK, Paquette LA. Development of an access route to the c31-c52 central core of amphidinol 3. Organic Letters. 9: 513-6. PMID 17249800 DOI: 10.1021/Ol062875+ |
0.351 |
|
2007 |
Paquette LA, Hu Y, Luxenburger A, Bishop RL. Studies toward the total synthesis of dumsin. 2. A second generation approach resulting in enantioselective construction of a functionalized ABC subunit of the tetranortriterpenoid insect antifeedant. The Journal of Organic Chemistry. 72: 209-22. PMID 17194102 DOI: 10.1021/Jo062068O |
0.427 |
|
2007 |
Nagamine T, Inomata K, Endo Y, Paquette LA. Amino acid mediated intramolecular asymmetric aldol reaction to construct a new chiral bicyclic enedione containing a seven-membered ring: remarkable inversion of enantioselectivity compared to the six-membered ring example. The Journal of Organic Chemistry. 72: 123-31. PMID 17194090 DOI: 10.1021/Jo061824N |
0.395 |
|
2007 |
Dura RD, Modolo I, Paquette LA. Effective synthetic routes to 4H- and 10bH- pyrido[2,1-α]isoindol-6-ones Heterocycles. 74: 145-148. DOI: 10.3987/Com-07-S(W)19 |
0.318 |
|
2007 |
Selvaraj PR, Paquette LA. Do upper limits to the multiple spiro acetalization of the cyclohexane ring exist? Heterocycles. 73: 165-168. DOI: 10.3987/Com-07-S(U)4 |
0.8 |
|
2007 |
Gentil S, Pirio N, Meunier P, Gallou F, Paquette LA. Ethene/norbornene copolymerization with (isodicyclopentadienyl)titanium complex-MAO catalyst Collection of Czechoslovak Chemical Communications. 72: 697-702. DOI: 10.1135/Cccc20070697 |
0.578 |
|
2007 |
Gallucci JC, Dura RD, Paquette LA. (11SR,13RS)-12-Oxa-9-aza-tetra-cyclo[7.4.1.02,7.0 11,13]tetra-deca-2(7),3,5-trien-8-one Acta Crystallographica Section E: Structure Reports Online. 63: o3417. DOI: 10.1107/S160053680703228X |
0.34 |
|
2007 |
Adaligil E, Davis BD, Hilmey DG, Shen Y, Spruell JM, Brodbelt JS, Houk KN, Paquette LA. Erratum: Synthesis of, and structural assignments to the stereoisomers of bis (2,2′)- and tris (2,2′,2″)-tetrahydrofurans: Conformational features and ionic binding capacities of these gateway polycyclic networks (Journal of Organic Chemistry (2007) 72 (6216)) Journal of Organic Chemistry. 72. DOI: 10.1021/Jo702007W |
0.311 |
|
2007 |
Hilmey DG, Paquette LA. 1,3‐Dichloroacetone as a Cyclopropanone Equivalent: 5‐Oxaspiro[3.4]Octan‐1‐One Organic Syntheses. 156-162. DOI: 10.1002/0471264229.Os084.16 |
0.391 |
|
2006 |
Paquette LA, Dura RD, Fosnaugh N, Stepanian M. Direct comparison of the response of bicyclic sultam and lactam dienes to photoexcitation. Concerning the propensity of differing bond types to bridgehead nitrogen for homolytic cleavage. The Journal of Organic Chemistry. 71: 8438-45. PMID 17064017 DOI: 10.1021/Jo061404Y |
0.392 |
|
2006 |
Kreilein MM, Hofferberth JE, Hart AC, Paquette LA. Diosphenol-based approach to the a-ring functionalization of advanced Taxol precursors. The Journal of Organic Chemistry. 71: 7329-36. PMID 16958527 DOI: 10.1021/Jo061115+ |
0.807 |
|
2006 |
Preston AJ, Gallucci JC, Paquette LA. Synthesis and selected reactions of a bicyclic sultam having sulfur at the apex position. The Journal of Organic Chemistry. 71: 6573-8. PMID 16901145 DOI: 10.1021/Jo0611162 |
0.433 |
|
2006 |
Hu Y, Bishop RL, Luxenburger A, Dong S, Paquette LA. Alkali metal counterion control of enolate protonation stereoselectivity. Organic Letters. 8: 2735-7. PMID 16774244 DOI: 10.1021/Ol060761S |
0.323 |
|
2006 |
Paquette LA, Zhang Y. From common carbohydrates to enantiopure cyclooctane polyols and glycomimetics via deoxygenative zirconocene ring contraction. The Journal of Organic Chemistry. 71: 4353-63. PMID 16749762 DOI: 10.1021/Jo051989G |
0.353 |
|
2006 |
Paquette LA, Hilmey DG, Gallucci JC. Practical designed syntheses of all stereoisomeric bis(2,2')- and tris(2,2',2' ')-tetrahydrofurans. Organic Letters. 8: 2635-7. PMID 16737332 DOI: 10.1021/Ol0608350 |
0.357 |
|
2006 |
Dong S, Parker GD, Tei T, Paquette LA. In pursuit of pestalotiopsin a via zirconocene-mediated ring contraction. Organic Letters. 8: 2429-31. PMID 16706543 DOI: 10.1021/Ol060827J |
0.401 |
|
2006 |
Dura RD, Paquette LA. Ring contraction of bridgehead sultams by photoinduced di-pi-methane rearrangement. The Journal of Organic Chemistry. 71: 2456-9. PMID 16526797 DOI: 10.1021/Jo0526587 |
0.365 |
|
2006 |
Hartung RE, Paquette LA. Direct comparison of SN2 mesylate displacement versus the mitsunobu protocol for 2′,3′-dideoxyspirocarbanucleoside construction Heterocycles. 67: 75-78. DOI: 10.3987/Com-04-S(T)2 |
0.798 |
|
2006 |
Hilmey DG, Selvaraj PR, Paquette LA. Synthesis and Lewis acid induced isomerization of mono-, di-, and tri-spiro α-keto tetrahydro-furans and -pyrans Canadian Journal of Chemistry. 84: 1388-1396. DOI: 10.1139/V06-103 |
0.816 |
|
2006 |
Dura RD, Paquette LA. Tetrabutylammonium fluoride in dimethyl sulfoxide: A reagent combination for the twofold dehydrobromination of vicinal dibromides Synthesis. 2837-2840. DOI: 10.1055/S-2006-942527 |
0.318 |
|
2006 |
Pichlmair S, de Lera Ruiz M, Vilotijevic I, Paquette LA. Exploration of conjugate addition routes to advanced tricyclic components of mangicol A Tetrahedron. 62: 5791-5802. DOI: 10.1016/J.Tet.2006.03.066 |
0.397 |
|
2006 |
Pichlmair S, de Lera Ruiz M, Basu K, Paquette LA. Evaluation of possible intramolecular [4+2] cycloaddition routes for assembling the central tetracyclic core of the potent marine antiinflammatory agent mangicol A Tetrahedron. 62: 5178-5194. DOI: 10.1016/J.Tet.2005.11.096 |
0.651 |
|
2005 |
Paquette LA, Liu Z, Ramsey C, Gallucci JC. Competitive stereochemical control operative during conrotatory electrocyclization of helically equilibrating diquinanyl-substituted 1,3,5,7-octatetraenyl bisenolates. The Journal of Organic Chemistry. 70: 8154-61. PMID 16277342 DOI: 10.1021/Jo0513919 |
0.332 |
|
2005 |
Paquette LA, Kreilein MM, Bedore MW, Friedrich D. Oxidative cleavage of p-methoxybenzyl ethers with methyl(trifluoromethyl)dioxirane. Organic Letters. 7: 4665-7. PMID 16209505 DOI: 10.1021/Ol051856H |
0.799 |
|
2005 |
Paquette LA, Dong S. Stereoselective synthesis of beta-anomeric 4'-thiaspirocyclic ribonucleosides carrying the full complement of RNA-level hydroxyl substitution. The Journal of Organic Chemistry. 70: 5655-64. PMID 15989350 DOI: 10.1021/Jo0506985 |
0.387 |
|
2005 |
Paquette LA, Chang SK. The polyol domain of amphidinol 3. A stereoselective synthesis of the entire C(1)-C(30) sector. Organic Letters. 7: 3111-4. PMID 15987218 DOI: 10.1021/Ol0511833 |
0.332 |
|
2005 |
Hilmey DG, Paquette LA. Promoter-dependent course of the Beckmann rearrangement of stereoisomeric spiro[4.4]nonane-1,6-dione monoximes. Organic Letters. 7: 2067-9. PMID 15876056 DOI: 10.1021/Ol050669G |
0.305 |
|
2005 |
Bondar D, Liu J, Müller T, Paquette LA. Pectenotoxin-2 synthetic studies. 2. Construction and conjoining of ABC and DE Eastern hemisphere subtargets. Organic Letters. 7: 1813-6. PMID 15844913 DOI: 10.1021/Ol0504291 |
0.804 |
|
2005 |
Hartung R, Paquette LA. Practical synthesis of enantiopure spiro[4.4]nonane C-(2'-deoxy)ribonucleosides. The Journal of Organic Chemistry. 70: 1597-604. PMID 15730277 DOI: 10.1021/Jo0480601 |
0.803 |
|
2005 |
Paquette LA, Zhang Y. Enantioselective route from carbohydrates to cyclooctane polyols. Organic Letters. 7: 511-3. PMID 15673277 DOI: 10.1021/Ol0474296 |
0.359 |
|
2005 |
Brennan NK, Guo X, Paquette LA. Second-generation, highly abbreviated route for elaboration of the oxetane D-ring in a fully functionalized taxane. The Journal of Organic Chemistry. 70: 732-4. PMID 15651832 DOI: 10.1021/Jo0482965 |
0.815 |
|
2005 |
Inomata K, Barragué M, Paquette LA. Diastereoselectivities realized in the amino acid catalyzed aldol cyclizations of triketo acetonides of differing ring size. The Journal of Organic Chemistry. 70: 533-9. PMID 15651798 DOI: 10.1021/Jo0486084 |
0.379 |
|
2005 |
Paquette LA, Liu Z, Efremov I. Exploratory studies aimed at a synthesis of vinigrol. 4. Probe of possible means for direct connection of the side arms and of ring-contraction alternatives. The Journal of Organic Chemistry. 70: 514-8. PMID 15651795 DOI: 10.1021/Jo048456C |
0.778 |
|
2005 |
Paquette LA, Efremov I. Exploratory studies aimed at a synthesis of vinigrol. 3. Evaluation of a lactone bridge as a conformational lock. The Journal of Organic Chemistry. 70: 510-3. PMID 15651794 DOI: 10.1021/Jo0484575 |
0.757 |
|
2005 |
Paquette LA, Efremov I, Liu Z. Exploratory studies aimed at a synthesis of vinigrol. 2. Attempts to exploit ring-closing metathesis for construction of the central cyclooctane belt. The Journal of Organic Chemistry. 70: 505-9. PMID 15651793 DOI: 10.1021/Jo048458X |
0.784 |
|
2005 |
Guo X, Paquette LA. Concise means for accessing an advanced precursor to 1-deoxypaclitaxel. The Journal of Organic Chemistry. 70: 315-20. PMID 15624939 DOI: 10.1021/Jo048289G |
0.41 |
|
2005 |
Paquette LA, Hilmey DG, Selvaraj PR. Direct access to heteropolycyclic spiroketones. 1,3-dichloroacetone as a cyclopropanone equivalent Heterocycles. 66: 57-60. DOI: 10.3987/Com-05-S(K)14 |
0.808 |
|
2005 |
Chang SK, Paquette LA. Synthesis of the skipped polyene chain and its neighboring highly oxygenated pyran ring en route to delivering the C(43)-C(67) subsector of amphidinol 3 Synlett. 2915-2918. DOI: 10.1055/S-2005-918960 |
0.397 |
|
2005 |
Hartung RE, Paquette LA. Development of a generic stereocontrolled pathway to fully hydroxylated spirocarbocyclic nucleosides as a prelude to RNA targeting Synthesis. 3209-3218. DOI: 10.1055/S-2005-918472 |
0.775 |
|
2005 |
Hilmey DG, Gallucci JC, Paquette LA. Neighboring effect of the lactam functionality in select reactions of 6-azaspiro[4.5]decane-1,7-dione Tetrahedron. 61: 11000-11009. DOI: 10.1016/J.Tet.2005.08.091 |
0.368 |
|
2005 |
Paquette LA, Selvaraj PR, Keller KM, Brodbelt JS. Is potential coordination of alkali metal ions to stereodefined polyoxygenated cyclohexanes an adequate driving force for fostering the adoption of axial conformers? Tetrahedron. 61: 231-240. DOI: 10.1016/J.Tet.2004.10.011 |
0.762 |
|
2005 |
Paquette LA, Tian Z, Seekamp CK, Wang T. Synthesis of the cyclopentyl nucleoside (-)-neplanocin A from D-glucose via zirconocene-mediated ring contraction Helvetica Chimica Acta. 88: 1185-1198. DOI: 10.1002/Hlca.200590099 |
0.798 |
|
2005 |
Paquette LA. The Ramberg‐Bäcklund Rearrangement Organic Reactions. 1-71. DOI: 10.1002/0471264180.Or025.01 |
0.404 |
|
2005 |
Kreilein MM, Eppich JC, Paquette LA. 1,4-Dioxene Organic Syntheses. 82: 99-107. |
0.768 |
|
2004 |
Paquette LA, Seekamp CK, Kahane AL, Hilmey DG, Gallucci J. Stereochemical features of Lewis acid-promoted glycosidations involving 4'-spiroannulated DNA building blocks. The Journal of Organic Chemistry. 69: 7442-7. PMID 15497968 DOI: 10.1021/Jo048904G |
0.798 |
|
2004 |
Paquette LA, Chang J, Liu Z. Synthetic studies aimed at (-)-cochleamycin A. Evaluation of late-stage macrocyclization alternatives. The Journal of Organic Chemistry. 69: 6441-8. PMID 15357606 DOI: 10.1021/Jo049084A |
0.586 |
|
2004 |
Paquette LA, Kahane AL, Seekamp CK. Conformationally constrained purine mimics. Incorporation of adenine and guanine into spirocyclic nucleosides. The Journal of Organic Chemistry. 69: 5555-62. PMID 15307723 DOI: 10.1021/Jo049413Z |
0.785 |
|
2004 |
Paquette LA, Barton WR, Gallucci JC. Synthesis of 1-Aza-8-thiabicyclo[4.2.1]nona-2,4-diene 8,8-dioxide and its conversion to a strained spirocycle via photoinduced SO2-N bond cleavage. Organic Letters. 6: 1313-5. PMID 15070325 DOI: 10.1021/Ol049679S |
0.402 |
|
2004 |
Paquette LA, Hartung RE, Hofferberth JE, Vilotijevic I, Yang J. Synthesis of stereoisomeric medium-ring alpha,alpha'-dihydroxy cycloalkanones. The Journal of Organic Chemistry. 69: 2454-60. PMID 15049645 DOI: 10.1021/Jo0358675 |
0.797 |
|
2004 |
Paquette LA, Hartung RE, Hofferberth JE, Gallucci JC. Reactions of alpha,alpha'-dihydroxy ketones with phosgene. Structural requirements for spiro epoxy carbonate formation. Organic Letters. 6: 969-71. PMID 15012077 DOI: 10.1021/Ol036497+ |
0.8 |
|
2004 |
Hartung RE, Paquette LA. Homologation of vicinal polyketone networks to epoxy ketones with diazomethane Heterocycles. 64: 23-26. DOI: 10.3987/Com-04-S(P)9 |
0.787 |
|
2004 |
Paquette LA. Spirocyclic Restriction of Nucleosides Australian Journal of Chemistry. 57: 7-17. DOI: 10.1071/Ch03267 |
0.353 |
|
2004 |
Basu K, Richards J, Paquette LA. Mono- and bis-acrolein derivatives by reliable and efficient one-step methylenation of aldehyde precursors Synthesis. 2841-2844. DOI: 10.1055/S-2004-834866 |
0.605 |
|
2004 |
Peng X, Bondar D, Paquette LA. Alkoxide precoordination to rhodium enables stereodirected catalytic hydrogenation of a dihydrofuranol precursor of the C29-40 F/G sector of pectenotoxin-2 Tetrahedron. 60: 9589-9598. DOI: 10.1016/J.Tet.2004.06.142 |
0.799 |
|
2004 |
Paquette LA, Kang HJ. Synthesis of an enantiomerically pure 2,2,4-trisubstituted cyclobutanone building block by zirconocene-promoted deoxygenative ring contraction of structurally modified 4-vinylfuranosides Tetrahedron. 60: 1353-1358. DOI: 10.1016/J.Tet.2003.07.012 |
0.357 |
|
2004 |
Gentil S, Pirio N, Meunier P, Gallou F, Paquette LA. Titanium isodicyclopentadienide hemimetallocenes for ethylene/styrene copolymerization European Polymer Journal. 40: 2241-2246. DOI: 10.1016/J.Eurpolymj.2004.01.024 |
0.578 |
|
2004 |
Hartung RE, Hilmey DG, Paquette LA. Fluoride ion-promoted α-ketol rearrangement during unmasking of silyl-protected medium-ring dihydroxy ketones Advanced Synthesis and Catalysis. 346: 713-716. DOI: 10.1002/Adsc.200404002 |
0.799 |
|
2004 |
Hofferberth JE, Paquette LA. The α‐Hydroxy Ketone (α‐Ketol) and Related Rearrangements † Organic Reactions. 62: 477-567. DOI: 10.1002/0471264180.Or062.03 |
0.769 |
|
2003 |
Paquette LA, Fabris F, Gallou F, Dong S. C4'-spiroalkylated nucleosides having sulfur incorporated at the apex position. The Journal of Organic Chemistry. 68: 8625-34. PMID 14575495 DOI: 10.1021/jo030196w |
0.623 |
|
2003 |
Paquette LA, Seekamp CK, Kahane AL. Conformational restriction of nucleosides by spirocyclic annulation at C4' including synthesis of the complementary dideoxy and didehydrodideoxy analogues. The Journal of Organic Chemistry. 68: 8614-24. PMID 14575494 DOI: 10.1021/Jo0301954 |
0.813 |
|
2003 |
Paquette LA, Hong FT. Total synthesis of dumsin. 1. Retrosynthetic strategy and the elaboration of key intermediates from (--)-bornyl acetate. The Journal of Organic Chemistry. 68: 6905-18. PMID 12946130 DOI: 10.1021/Jo0301346 |
0.391 |
|
2003 |
Paquette LA, Guevel R, Sakamoto S, Kim IH, Crawford J. Convergent enantioselective synthesis of vinigrol, an architecturally novel diterpenoid with potent platelet aggregation inhibitory and antihypertensive properties. 1. Application of anionic sigmatropy to construction of the octalin substructure. The Journal of Organic Chemistry. 68: 6096-107. PMID 12895037 DOI: 10.1021/Jo0301301 |
0.394 |
|
2003 |
Paquette LA, Shetuni BB, Gallucci JC. pi-Facial stereoselectivity in Diels-Alder cycloadditions to 1-oxaspiro[4.5]deca-6,9-dien-8-one. The strong directive effect of ether oxygen in a cross-conjugated ketone setting. Organic Letters. 5: 2639-42. PMID 12868878 DOI: 10.1021/Ol0347895 |
0.397 |
|
2003 |
Gallucci JC, Gentil S, Pirio N, Meunier P, Gallou F, Paquette LA. ansa-[(tert-Butylamino)(isodicyclopentadienyl)dimethylsilane]Zr(NMe2)2 prepared by an amine-elimination reaction. Acta Crystallographica. Section C, Crystal Structure Communications. 59: M109-11. PMID 12682383 DOI: 10.1107/S0108270103003172 |
0.614 |
|
2003 |
Paquette LA, Lo HY. Chemical modification of a highly functionalized taxane. The consequences of an absent bridgehead double bond on oxetane D-ring construction. The Journal of Organic Chemistry. 68: 2282-9. PMID 12636392 DOI: 10.1021/jo0206566 |
0.325 |
|
2003 |
Paquette LA, Lo HY, Hofferberth JE, Gallucci JC. A delicate balance of energetics. Subtleties associated with alpha-ketol-based bridge migration to afford 9-keto-10beta-p-methoxybenzyloxytaxanes. The Journal of Organic Chemistry. 68: 2276-81. PMID 12636391 DOI: 10.1002/CHIN.200326194 |
0.749 |
|
2003 |
Paquette LA, Hofferberth JE. Effect of 9,10-cyclic acetal stereochemistry on feasible operation of the alpha-ketol rearrangement in highly functionalized paclitaxel (Taxol) precursors. The Journal of Organic Chemistry. 68: 2266-75. PMID 12636390 DOI: 10.1021/jo020627v |
0.734 |
|
2003 |
Paquette LA, Hartung RE, France DJ. Conversion of the enantiomers of spiro[4.4]nonane-1,6-diol into both epimeric carbaspironucleosides having natural C1' absolute configuration. Organic Letters. 5: 869-71. PMID 12633093 DOI: 10.1021/Ol0340033 |
0.804 |
|
2003 |
Guo X, Basu K, Cabral JA, Paquette LA. Relative rate profile for ring-closing metathesis of a series of 1-substituted 1,7-octadienes as promoted by a 4,5-dihydroimidazol-2-ylidene-coordinated ruthenium catalyst. Organic Letters. 5: 789-92. PMID 12633072 DOI: 10.1021/Ol0272794 |
0.612 |
|
2003 |
Paquette LA, Vilotijevic I, Hilmey D, Yang J. Divergent regioselectivity in the base-promoted reactions of cyclic eight-membered alpha-ketols with activated halides. Organic Letters. 5: 463-6. PMID 12583744 DOI: 10.1021/Ol027315Z |
0.543 |
|
2003 |
Gallucci JC, Gentil S, Pirio N, Meunier P, Gallou F, Paquette LA. A doubly bridged isodicyclopentadienyl zirconium complex: bis[N-(3,5-dimethylphenyl)-N-[(eta5-isodicyclopentadien-2-yl)dimethylsilyl]amido-kappaN]zirconium(II) diethyl ether solvate. Acta Crystallographica. Section C, Crystal Structure Communications. 59: m67-9. PMID 12574651 DOI: 10.1107/S0108270103000751 |
0.597 |
|
2003 |
Yang J, Long YO, Paquette LA. Concise total syntheses of the bioactive mesotricyclic diterpenoids jatrophatrione and citlalitrione. Journal of the American Chemical Society. 125: 1567-74. PMID 12568617 DOI: 10.1021/Ja021177R |
0.683 |
|
2003 |
Paquette LA, Kim IH, Cunière N. Zirconocene-mediated route to enantiopure 9-oxabicyclononanes functionalized on both carbon bridges. Organic Letters. 5: 221-3. PMID 12529145 DOI: 10.1021/Ol027336T |
0.805 |
|
2003 |
Paquette LA, Webber P, Simpson I. Contrasting diastereofacial selectivity associated with N-phenyltriazolinedione cycloadditions to oxaspirocycloheptatrienes. Organic Letters. 5: 177-80. PMID 12529134 DOI: 10.1021/Ol020223P |
0.366 |
|
2003 |
Gallucci JC, Gentil S, Pirio N, Meunier P, Gallou F, Paquette LA. ansa-[(tert-butylamino)(isodicyclopentadienyl)dimethylsilane]Zr(NMe2 )2 prepared by an amine-elimination reaction Acta Crystallographica Section C: Crystal Structure Communications. 59: m109-m111. DOI: 10.1107/S0108270103003172 |
0.598 |
|
2003 |
Gallucci JC, Gentil S, Pirio N, Meunier P, Gallou F, Paquette LA. A doubly bridged isodicyclopentadienyl zirconium complex: bis{N-(3,5-dimethylphenyl)-N-[(η5-isodicyclopentadien-2-yl) dimethylsilyl]amido-κN}zirconium(II) diethyl ether solvate Acta Crystallographica Section C: Crystal Structure Communications. 59: m67-m69. DOI: 10.1107/S0108270103000751 |
0.513 |
|
2003 |
Vilotijevic I, Yang J, Hilmey D, Paquette LA. Base-promoted ring contraction of eight-membered cyclic acyloins and their ethers to Cs-symmetric α-ketols Synthesis. 1872-1874. DOI: 10.1055/S-2003-41003 |
0.502 |
|
2003 |
Paquette LA. Fundamental mechanistic characteristics and synthetic applications of allylations promoted by indium metal in aqueous media Synthesis. 765-774. DOI: 10.1055/S-2003-38061 |
0.395 |
|
2003 |
Bennett GD, Paquette LA. Allylindation in Aqueous Media: Methyl 3‐(Hydroxymethyl)‐4‐Methyl‐2‐Methylenepentanoate Organic Syntheses. 107-107. DOI: 10.1002/0471264180.Os077.11 |
0.302 |
|
2003 |
Behrens C, Paquette LA. N‐Benzyl‐2,3‐Azetidinedione Organic Syntheses. 106-106. DOI: 10.1002/0471264180.Os075.13 |
0.344 |
|
2003 |
Dahnke KR, Paquette LA. Inverse Electron‐Demand Diels‐Alder Cycloaddition of a Ketene Dithioacetal. Copper Hydride‐Promoted Reduction of a Conjugated Enone. 9‐Dithiolanobicyclo[3.2.2]Non‐6‐En‐2‐One from Tropone Organic Syntheses. 181-181. DOI: 10.1002/0471264180.Os071.23 |
0.349 |
|
2003 |
Dahnke KR, Paquette LA. 2‐Methylene‐1,3‐Dithiolane Organic Syntheses. 175-175. DOI: 10.1002/0471264180.Os071.22 |
0.394 |
|
2003 |
Poupart M, Lassalle G, Paquette LA. Intramolecular Oxidative Coupling of a Bisenolate: 4‐Methyltricyclo[2.2.2.03,5]Octane‐2,6‐dione Organic Syntheses. 220-220. DOI: 10.1002/0471264180.Os068.27 |
0.397 |
|
2003 |
Lin H, Paquette LA. Reductive Annulation of Vinyl Sulfones: Bicyclo[4.3.0.]non‐1‐en‐4‐one Organic Syntheses. 163-163. DOI: 10.1002/0471264180.Os067.21 |
0.345 |
|
2003 |
Lin H, Coghlan MJ, Paquette LA. Dienophile Activation via Selenosulfonation: 1‐(Phenylsulfonyl)cyclopentene Organic Syntheses. 157-157. DOI: 10.1002/0471264180.Os067.20 |
0.311 |
|
2003 |
Paquette LA, Carr RVC. Phenyl Vinyl Sulfone and Sulfoxide Organic Syntheses. 157-157. DOI: 10.1002/0471264180.Os064.24 |
0.318 |
|
2003 |
Taylor RT, Paquette LA. 1,6‐Dimethyltricyclo[4.1.0.01,6]hept‐3‐ene Organic Syntheses. 39-39. DOI: 10.1002/0471264180.Os061.09 |
0.335 |
|
2003 |
Photis JM, Paquette LA. 1,2‐Dimethylcyclobutenes by Reductive Ring‐Contraction of Sulfolanes: cis‐7,8‐Dimethylbicyclo[4.2.0]oct‐7‐ene Organic Syntheses. 53-53. DOI: 10.1002/0471264180.Os057.14 |
0.324 |
|
2003 |
Paquette LA, Barrett JH. 2,7-Dimethyloxepin Organic Syntheses. 62-62. DOI: 10.1002/0471264180.Os049.17 |
0.422 |
|
2003 |
Paquette LA, Wittenbrook LS. 2‐Chlorothiirane 1,1‐dioxide Organic Syntheses. 18-18. DOI: 10.1002/0471264180.Os049.06 |
0.332 |
|
2003 |
Paquette LA. 1,3‐Dihydro‐3,5,7‐Trimethyl‐2H‐Azepin‐2‐One Organic Syntheses. 41-41. DOI: 10.1002/0471264180.Os044.13 |
0.33 |
|
2002 |
Paquette LA, Geng F. A highly abbreviated synthesis of pentalenene by means of the squarate ester cascade. Organic Letters. 4: 4547-9. PMID 12465934 DOI: 10.1021/Ol020208K |
0.615 |
|
2002 |
Paquette LA, Geng F. Applications of the squarate ester cascade to the expeditious synthesis of hypnophilin, coriolin, and ceratopicanol. Journal of the American Chemical Society. 124: 9199-203. PMID 12149025 DOI: 10.1021/Ja020474T |
0.614 |
|
2002 |
Paquette LA, Yang J, Long YO. Concerning the antileukemic agent jatrophatrione: the first total synthesis of a [5.9.5] tricyclic diterpene. Journal of the American Chemical Society. 124: 6542-3. PMID 12047168 DOI: 10.1021/Ja020292Z |
0.649 |
|
2002 |
Paquette LA, Cunière N. Diastereoselectivity control in the zirconocene-mediated ring contraction of 4-vinylfuranosides to enantiopure multiply functionalized cyclobutanes. Organic Letters. 4: 1927-9. PMID 12027649 DOI: 10.1021/Ol020063H |
0.813 |
|
2002 |
Paquette LA, Duan M, Konetzki I, Kempmann C. A convergent three-component total synthesis of the powerful immunosuppressant (-)-sanglifehrin a. Journal of the American Chemical Society. 124: 4257-70. PMID 11960455 DOI: 10.1021/Ja020091V |
0.601 |
|
2002 |
Paquette LA, Peng X, Bondar D. Pectenotoxin-2 synthetic studies. 1. Alkoxide precoordination to [Rh(NBD)(DIPHOS-4)]BF(4) allows directed hydrogenation of a 2,3-dihydrofuran-3-ol without competing furan production. Organic Letters. 4: 937-40. PMID 11893190 DOI: 10.1021/Ol010302L |
0.802 |
|
2002 |
Chang J, Paquette LA. Studies aimed at the total synthesis of the antitumor antibiotic cochleamycin A. An enantioselective biosynthesis-based pathway to the AB bicyclic core. Organic Letters. 4: 253-6. PMID 11796063 DOI: 10.1021/Ol0102592 |
0.509 |
|
2002 |
Geng F, Liu J, Paquette LA. Three-component coupling via the squarate ester cascade as a concise route to the bioactive triquinane sesquiterpene hypnophilin. Organic Letters. 4: 71-3. PMID 11772093 DOI: 10.1021/Ol0102388 |
0.6 |
|
2002 |
Cho IH, Paquette LA. Highly functionalized pyrans designed for multipoint side chain attachment to the F-ring sector of spongistatin 1 (altohyrtin A) Heterocycles. 58: 43-46. DOI: 10.3987/Com-01-S(M)6 |
0.58 |
|
2002 |
Efremov I, Paquette LA. A regioselective route to 2,3,4-trisubstituted furans Heterocycles. 56: 35-38. DOI: 10.3987/Com-00-S(K)2 |
0.747 |
|
2002 |
Paquette LA, Arbit RM, Funel JA, Bolshakov S. The carbohydrate-sesquiterpene interface. A zirconocene-mediated synthesis of (+)-epiafricanol from D-glucose Synthesis. 2105-2109. DOI: 10.1055/S-2002-34380 |
0.798 |
|
2002 |
Boulet SL, Paquette LA. Toward a total synthesis of okilactomycin. 2. A metathesis-based approach to the heavily functionalized cyclohexane ring Synthesis. 895-900. DOI: 10.1055/S-2002-28511 |
0.445 |
|
2002 |
Paquette LA, Boulet SL. Toward a total synthesis of okilactomycin. 1. A direct, enantiocontrolled route to the western sector Synthesis. 888-894. DOI: 10.1055/S-2002-28510 |
0.403 |
|
2002 |
Gentil S, Dietz M, Pirio N, Meunier P, Gallucci JC, Gallou F, Paquette LA. A silylene-bridged (isodicyclopentadienyl)(fluorenyl) complex of zirconium for homogeneous olefin polymerization Organometallics. 21: 5162-5166. DOI: 10.1021/Om020384X |
0.607 |
|
2002 |
Basu K, Cabral JA, Paquette LA. Comparative investigation of kinetic consequences associated with long-range electronic effects on catalytic ruthenium-promoted ring-closing metathesis Tetrahedron Letters. 43: 5453-5456. DOI: 10.1016/S0040-4039(02)01064-X |
0.623 |
|
2002 |
Horáček M, Štěpnička P, Gentil S, Fejfarová K, Kubišta J, Pirio N, Meunier P, Gallou F, Paquette LA, Mach K. Syntheses and properties of some exo,exo-bis(isodicyclopentadienyl)titanium low-valent complexes Journal of Organometallic Chemistry. 656: 81-88. DOI: 10.1016/S0022-328X(02)01562-0 |
0.608 |
|
2002 |
Paquette LA, Boggs RA, Ward JS. Silver(I) Ion Catalyzed Rearrangements Of Strained Sigma Bonds Part 30, Rhodium(I)- And Palladium(Ii)-Promoted Rearrangements Of Homocubanes, A Comparison Of Kinetic Reactivity And Product Distribution With Substituent Alteration Cheminform. 6. DOI: 10.1002/Chin.197520158 |
0.308 |
|
2002 |
Basu K, Eppich JC, Paquette LA. Ruthenium-promoted ring-closing metathesis of ene-dienes. Competitive intramolecular regioselection as a function of chain length Advanced Synthesis and Catalysis. 344: 615-618. DOI: 10.1002/1615-4169(200208)344:6/7<615::Aid-Adsc615>3.0.Co;2-O |
0.631 |
|
2002 |
Paquette LA, Basu K, Eppich JC, Hofferberth JE. Systematic analysis of the intramolecular competition associated with the ring closing metathesis of ene-diene systems of differing chain length with a pair of ruthenium catalysts Helvetica Chimica Acta. 85: 3033-3051. DOI: 10.1002/1522-2675(200210)85:10<3033::Aid-Hlca3033>3.0.Co;2-2 |
0.787 |
|
2001 |
Paquette LA, Owen DR, Bibart RT, Seekamp CK. Spirocyclic restriction of nucleosides. An analysis of protecting group feasibility while accessing prototype anti-1-oxaspiro[4.4]nonanyl mimics. Organic Letters. 3: 4043-5. PMID 11735580 DOI: 10.1021/Ol010212G |
0.808 |
|
2001 |
Paquette LA, Bibart RT, Seekamp CK, Kahane AL. Spirocyclic restriction of nucleosides. Synthesis of the first exemplary syn-1-oxaspiro[4.4]nonanyl member. Organic Letters. 3: 4039-41. PMID 11735579 DOI: 10.1021/Ol010209X |
0.809 |
|
2001 |
Paquette LA, Ra CS, Gallucci JC, Kang HJ, Ohmori N, Arrington MP, David W, Brodbelt JS. Constraining of small-ring cyclic ether triads by stereodefined spiroannulation to an inositol orthoformate platform. Solution- and gas-phase alkali metal binding affinities for three- to five-membered ring structural combinations. The Journal of Organic Chemistry. 66: 8629-39. PMID 11735548 DOI: 10.1021/Jo0107507 |
0.305 |
|
2001 |
Duan M, Paquette LA. Enantioselective Total Synthesis of the Cyclophilin-Binding Immunosuppressive Agent Sanglifehrin A This work was financially supported by Eli Lilly and Company and a Robert Mayer Graduate Fellowship (to M.D.). We thank Prof. K. C. Nicolaou for providing authentic spectra of 1. Angewandte Chemie (International Ed. in English). 40: 3632-3636. PMID 11592204 DOI: 10.1002/1521-3773(20011001)40:19<3632::Aid-Anie3632>3.0.Co;2-5 |
0.551 |
|
2001 |
Balskus EP, Méndez-Andino J, Arbit RM, Paquette LA. Intercalation of multiple carbon atoms between the carbonyls of alpha-diketones. The Journal of Organic Chemistry. 66: 6695-704. PMID 11578223 DOI: 10.1021/Jo010494Y |
0.825 |
|
2001 |
Bernardelli P, Moradei OM, Friedrich D, Yang J, Gallou F, Dyck BP, Doskotch RW, Lange T, Paquette LA. Total asymmetric synthesis of the putative structure of the cytotoxic diterpenoid (-)-sclerophytin a and of the authentic natural sclerophytins A and B. Journal of the American Chemical Society. 123: 9021-32. PMID 11552810 DOI: 10.1021/Ja011285Y |
0.734 |
|
2001 |
Paquette LA, Efremov I. Teubrevin G and teubrevin H: the first total syntheses of rearranged neo-clerodanes including solutions to the problems of chirality merger and furan ring assembly. Journal of the American Chemical Society. 123: 4492-501. PMID 11457235 DOI: 10.1021/Ja010313+ |
0.78 |
|
2001 |
Gallou F, MacMillan DW, Overman LE, Paquette LA, Pennington LD, Yang J. Enantioselective syntheses of authentic sclerophytin A, sclerophytin B, and cladiell-11-ene-3,6,7-triol. Organic Letters. 3: 135-7. PMID 11429857 DOI: 10.1021/Ol000345M |
0.684 |
|
2001 |
Hofferberth JE, Lo HY, Paquette LA. Stereospecific anionically promoted transannular hydride shifts in medium-ring hydroxy ketones. Probe of their reversibility and the potential for regiocontrol. Organic Letters. 3: 1777-80. PMID 11405709 DOI: 10.1021/Ol0100733 |
0.754 |
|
2001 |
Paquette LA, Ra CS, Schloss JD, Leit SM, Gallucci JC. Direct synthesis of previously inaccessible bridgehead azabicyclics by intramolecular cyclization of alpha-sulfonamido and alpha-sulfonimido radicals. The Journal of Organic Chemistry. 66: 3564-73. PMID 11348146 DOI: 10.1021/Jo010216Z |
0.822 |
|
2001 |
Paquette LA, Owen DR, Bibart RT, Seekamp CK, Kahane AL, Lanter JC, Corral MA. 1-Oxaspiro[4.4]nonan-6-ones. Synthetic access via oxonium ion technology, optical resolution, and conversion into enantiopure spirocyclic alpha,beta-butenolides. The Journal of Organic Chemistry. 66: 2828-34. PMID 11304208 DOI: 10.1021/Jo010026O |
0.792 |
|
2001 |
Paquette LA, Méndez-Andino J. Synthesis of paddlanes having a bicyclo[1.1.1]pentane core. The consequences of olefin metathesis involving unsaturated 1,3-dicarboxylate esters of varying chain length Tetrahedron Letters. 42: 967-970. DOI: 10.1016/S0040-4039(00)02212-7 |
0.383 |
|
2001 |
Duan M, Paquette LA. Enantioselective Total Synthesis of the Cyclophilin-Binding Immunosuppressive Agent Sanglifehrin A Angewandte Chemie. 113: 3744-3748. DOI: 10.1002/1521-3757(20011001)113:19<3744::Aid-Ange3744>3.0.Co;2-B |
0.499 |
|
2000 |
Rablen PR, Paquette LA, Borden WT. Why Doesn't all-trans-1,2,3,4,5,6-Hexaspiro(THF)cyclohexane complex metal ions? The Journal of Organic Chemistry. 65: 9180-5. PMID 11149867 DOI: 10.1021/Jo001432V |
0.324 |
|
2000 |
Paquette LA, Tae J, Branan BM, Bolin DG, Eisenberg SW. Synthesis and conformational properties of several maximally substituted hexa(spirotetrahydrofuranyl)cyclohexanes. Assessment Of the pronounced bias of the all-trans D(3)(d)()-symmetric isomer for total equatorial oxygen occupancy The Journal of Organic Chemistry. 65: 9172-9. PMID 11149866 DOI: 10.1021/Jo0014313 |
0.394 |
|
2000 |
Paquette LA, Tae J, Hickey ER, Trego WE, Rogers RD. Preorganized ligand arrays based on spirotetrahydrofuranyl motifs. Synthesis of the stereoisomeric 1,8,14-trioxatrispiro[4.1.4.1.4. 1]octadecanes and the contrasting conformational features and ionic binding capacities of these belted ionophores. The Journal of Organic Chemistry. 65: 9160-71. PMID 11149865 DOI: 10.1021/Jo001430A |
0.349 |
|
2000 |
Schloss JD, Leit SM, Paquette LA. Radical and anionic response of N-(Bromomethanesulfonyl)-substituted alpha,alpha'-bridged piperidine substrates The Journal of Organic Chemistry. 65: 7119-23. PMID 11031038 DOI: 10.1021/Jo000873B |
0.798 |
|
2000 |
Paquette LA, Moradei OM, Bernardelli P, Lange T. Synthesis of the alleged structure of sclerophytin A. The setting of two oxygen bridges within the fused cyclodecanol B ring is not Nature's Way. Organic Letters. 2: 1875-8. PMID 10891180 DOI: 10.1021/Ol000083O |
0.353 |
|
2000 |
Paquette LA, Ohmori N, Lowinger TB, Rogers RD. Vicinal tetrahydrofuranyl substitution of alkyl chains. Tetra-, penta-, and hexafunctionalized arrays. The Journal of Organic Chemistry. 65: 4303-8. PMID 10891130 DOI: 10.1021/Jo0001075 |
0.395 |
|
2000 |
Zuev D, Paquette LA. A modular approach to marine macrolide construction. 3. Enantioselective synthesis of the C1-C28 sector of spongistatin 1 (altohyrtin A). Organic Letters. 2: 679-82. PMID 10814408 DOI: 10.1021/Ol0000049 |
0.717 |
|
2000 |
Mendez-Andino J, Paquette LA. Tandem deployment of indium-, ruthenium-, and lead-promoted reactions. Four-carbon intercalation between the carbonyl groups of open-chain and cyclic alpha-diketones Organic Letters. 2: 1263-5. PMID 10810723 DOI: 10.1021/Ol000037O |
0.362 |
|
2000 |
Paquette LA, Schloss JD, Efremov I, Fabris F, Gallou F, Mendez-Andino J, Yang J. A convenient method for removing all highly-colored byproducts generated during olefin metathesis reactions Organic Letters. 2: 1259-61. PMID 10810722 DOI: 10.1021/Ol000036W |
0.801 |
|
2000 |
Cunière N, Paquette LA. The case for noncompetitive cyclizative options during attempted expedient construction of the core ring system of CP-263,114 Arkivoc. 2000: 274-281. DOI: 10.3998/Ark.5550190.0001.311 |
0.822 |
|
2000 |
Gentil S, Pirio N, Meunier P, Gallucci JG, Schloss JD, Paquette LA. Stereoselective access to new half-sandwich complexes containing an isodicyclopentadienyl ligand Organometallics. 19: 4169-4172. DOI: 10.1021/Om000472M |
0.779 |
|
2000 |
Schloss JD, Leit SM, Paquette LA. Radical and anionic response of N-(bromomethanesulfonyl)-substituted α,α'-bridged piperidine substrates Journal of Organic Chemistry. 65: 7119-7123. DOI: 10.1021/jo000873b |
0.771 |
|
2000 |
Paquette LA, Fabris F, Tae J, Gallucci JC, Hofferberth JE. Catalytic ring-closing metathesis of doubly armed, bridged bicyclic sulfones. Evaluation of chain length and possible intramolecular SO2 group ligation to the ruthenium carbenoid Journal of the American Chemical Society. 122: 3391-3398. DOI: 10.1021/Ja9943849 |
0.772 |
|
2000 |
Paquette LA, Zhao Z, Gallou F, Liu J. New photorearrangements of 2-cyclopentenones. The genesis and fate of cyclopropylcarbinyl biradical intermediates [1] Journal of the American Chemical Society. 122: 1540-1541. DOI: 10.1021/Ja994081E |
0.603 |
|
2000 |
Paquette LA, Tae J, Arrington MP, Sadoun AH. Enantioselective double Michael addition/cyclization with an oxygen- centered nucleophile as the first step in a concise synthesis of natural (+)- asteriscanolide Journal of the American Chemical Society. 122: 2742-2748. DOI: 10.1021/Ja994053W |
0.437 |
|
2000 |
Paquette LA, Barriault L, Pissarnitski D, Johnston JN. Stereocontrolled elaboration of natural (-)-polycavernoside A, a powerfully toxic metabolite of the red alga Polycavernosa tsudai Journal of the American Chemical Society. 122: 619-631. DOI: 10.1021/Ja993487O |
0.761 |
|
2000 |
Paquette LA, Reddy YR, Vayner G, Houk KN. High-rate accelerations in oxy-Cope rearrangements induced by sulfur substitution: Kinetic study involving electronically and geometrically differentiated 1-alkenyl-2-(Z-1-propenyl)-7,7-dimethyl-exo-norbornan-2-ols Journal of the American Chemical Society. 122: 10788-10794. DOI: 10.1021/Ja0025402 |
0.349 |
|
2000 |
Efremov I, Paquette LA. First synthesis of a rearranged neo-clerodane diterpenoid. Development of totally regioselective trisubstituted furan ring assembly and medium-ring alkylation tactics for efficient access to (-)-teubrevin G [15] Journal of the American Chemical Society. 122: 9324-9325. DOI: 10.1021/Ja002450X |
0.382 |
|
2000 |
Paquette LA, Gallou F, Zhao Z, Young DG, Liu J, Yang J, Friedrich D. Propensity of 4-methoxy-4-vinyl-2-cyclopentenones housed in tri- and Tetracyctic frameworks for deep-seated photochemical rearrangement Journal of the American Chemical Society. 122: 9610-9620. DOI: 10.1021/Ja001813Q |
0.699 |
|
2000 |
Duan M, Paquette LA. Highly diastereocontrolled synthesis of the C1-C25 domain of sanglifehrin A Tetrahedron Letters. 41: 3789-3792. DOI: 10.1016/S0040-4039(00)00504-9 |
0.561 |
|
2000 |
Paquette L, Zeng Q, Wang H, Shih T. From Carbohydrates to the Discovery of Pronounced Heteroatomic Effects on Anionically Accelerated [3,3]-Sigmatropic Rearrangements European Journal of Organic Chemistry. 2000: 2187-2194. DOI: 10.1002/1099-0690(200006)2000:12<2187::Aid-Ejoc2187>3.0.Co;2-2 |
0.408 |
|
2000 |
Gallou F, Rigby JH, Paquette LA, Warshakoon NC, Payen AJ, Fales KR, Pigge CF. [6π + 2π] and [6π + 4π] higher-order cycloadditions and their deployment in total synthesis Chemtracts. 13: 223-228. |
0.568 |
|
2000 |
Yamazaki T, Kuboki A, Ohta H, Mitzel TM, Paquette LA, Sugai T. Yamadazyma farinosa IFO 10896-mediated reduction of 4,4-dimethoxy-2- butanone as the key-step for the preparation of 1,3-diols with unsymmetrical substituents Synthetic Communications. 30: 3061-3072. |
0.787 |
|
2000 |
Long YO, Paquette LA. Non-enzymatic kinetic resolution of racemic alcohols with chiral catalysts Chemtracts. 13: 1-8. |
0.409 |
|
1999 |
Paquette LA, Tae J, Branan BM, Eisenberg SWE, Hofferberth JE. Synthesis and Conformational Properties of the Sterically Crowded D -Symmetric all-trans Hexa(spirotetrahydrofuranyl)cyclohexane System. Angewandte Chemie (International Ed. in English). 38: 1412-1414. PMID 29711563 DOI: 10.1002/(Sici)1521-3773(19990517)38:10<1412::Aid-Anie1412>3.0.Co;2-X |
0.746 |
|
1999 |
Paquette LA, Edmondson SD, Monck N, Rogers RD. Studies Directed toward the Synthesis of the Unusual Antileukemic Diterpene Jatrophatrione. 2. Functionalization of Advanced Polycyclic Precursors to the 9-Epi and 8,9-Dehydro Congeners. The Journal of Organic Chemistry. 64: 3255-3265. PMID 11674428 DOI: 10.1021/Jo982526W |
0.316 |
|
1999 |
Paquette LA, Nakatani S, Zydowsky TM, Edmondson SD, Sun LQ, Skerlj R. Studies Directed toward the Synthesis of the Unusual Antileukemic Diterpene Jatrophatrione. 1. A Solution to the Problem of Chirality Merger during Elaboration of the Entire Carbotricyclic Framework. The Journal of Organic Chemistry. 64: 3244-3254. PMID 11674427 DOI: 10.1021/Jo9825254 |
0.418 |
|
1999 |
Paquette LA, Brand S, Behrens C. An Enantioselective Ring Expansion Route Leading to Furanose and Pyranose Nucleosides Featuring Spirodiketopiperazines at the Anomeric Position. The Journal of Organic Chemistry. 64: 2010-2025. PMID 11674296 DOI: 10.1021/Jo982259U |
0.419 |
|
1999 |
Paquette LA, Rothhaar RR. Competitive Intramolecular/Intermolecular Chelation Options Operative during Indium-Promoted Additions to Pyridyl Aldehydes and to Glyoxylic Acid under Aqueous Conditions. The Journal of Organic Chemistry. 64: 217-224. PMID 11674106 DOI: 10.1021/Jo981717W |
0.388 |
|
1999 |
Barriault L, Boulet SL, Fujiwara K, Murai A, Paquette LA, Yotsu-Yamashita M. Synthesis and biological evaluation of analogs of the marine toxin polycavernoside A. Bioorganic & Medicinal Chemistry Letters. 9: 2069-72. PMID 10450983 DOI: 10.1016/S0960-894X(99)00341-8 |
0.635 |
|
1999 |
Zeng Q, Paquette LA. Selective Acylation Reactions of an Isotaxane Tetraol. A Direct Pathway to Introduction of the Oxetane Ring Synlett. 1999: 1547-1550. DOI: 10.1055/S-1999-2911 |
0.37 |
|
1999 |
Gobley O, Gentil S, Schloss JD, Rogers RD, Gallucci JC, Meunier P, Gautheron B, Paquette LA. Magnesiation of isodicyclopentadiene. Formation of sandwich and monomeric complexes and the stereoselectivity of their reactions with transition metal halides Organometallics. 18: 2531-2535. DOI: 10.1021/Om990200N |
0.787 |
|
1999 |
Paquette LA, Brand S, Behrens C. An enantioselective ring expansion route leading to furanose and pyranose nucleosides featuring spirodiketopiperazines at the anomeric position Journal of Organic Chemistry. 64: 2010-2025. DOI: 10.1021/jo982259u |
0.326 |
|
1999 |
Paquette LA, Barriault L, Pissarnitski D. A convergent total synthesis of the macrolactone disaccharide toxin (- )-polycavernoside A Journal of the American Chemical Society. 121: 4542-4543. DOI: 10.1021/Ja990384X |
0.655 |
|
1999 |
Paquette LA, Konetzki I, Duan M. Synthesis of the tripeptide (C1-N12) and hydroxylated hexadecene (C26-C41) domains of sanglifehrin A and C Tetrahedron Letters. 40: 7441-7444. DOI: 10.1016/S0040-4039(99)01539-7 |
0.517 |
|
1999 |
Paquette LA, Jinsung T. A head-to-head comparison of α- and β-alkoxy effects on stereoselectivity. Nucleophilic additions to a cyclohexanone substituted with five axial C-O bonds Tetrahedron Letters. 40: 5971-5974. DOI: 10.1016/S0040-4039(99)01167-3 |
0.335 |
|
1999 |
Paquette LA, Usui S. Tandem use of reductive and radical cyclization protocols in an approach to the first σ-allyl cation Tetrahedron Letters. 40: 3499-3502. DOI: 10.1016/S0040-4039(99)00541-9 |
0.38 |
|
1999 |
Paquette LA, Tae J, Branan BM, Eisenberg SWE, Hofferberth JE. Synthesis and conformational properties of the sterically crowded D(3d)- symmetric all-trans hexa(spirotetrahydrofuranyl)cyclohexane system Angewandte Chemie - International Edition. 38: 1412-1414. DOI: 10.1002/(SICI)1521-3773(19990517)38:10<1412::AID-ANIE1412>3.0.CO;2-X |
0.7 |
|
1999 |
Paquette LA, Tae J, Branan BM, Eisenberg SWE, Hofferberth JE. Synthese und konformative Eigenschaften des sterisch überladenen,D3d-symmetrischen all-trans-Hexa(spirotetrahydrofuranyl)cyclohexans Angewandte Chemie. 111: 1505-1507. DOI: 10.1002/(Sici)1521-3757(19990517)111:10<1505::Aid-Ange1505>3.0.Co;2-Q |
0.725 |
|
1999 |
Zuev D, Bender JA, Paquette LA, Blize AE, Browder CC, Giese S, West FG, Wang Y, Arif AM. First examples of the interrupted Nazarov reaction Chemtracts. 12: 1019-1025. |
0.666 |
|
1998 |
Zeng Q, Bailey S, Wang TZ, Paquette LA. Bicyclic Systems Related to Taxol. A Direct Means for Implementing C-2 Oxygenation and Demonstration of the Feasibility of alpha-Ketol Equilibration in a Fully Oxygenated B-Ring Setting. The Journal of Organic Chemistry. 63: 137-143. PMID 11674054 DOI: 10.1021/Jo971592F |
0.337 |
|
1998 |
Johnston JN, Tsui HC, Paquette LA. Application of an S --> O Allylic Transposition in the Context of a Bridgehead Olefinic System. New Opportunities for the Structural Modification of Bicyclo[6.2.1]undecanes via Transannular Ring Closure. The Journal of Organic Chemistry. 63: 129-136. PMID 11674053 DOI: 10.1021/Jo971591N |
0.623 |
|
1998 |
Paquette LA, Pissarnitski D, Barriault L. A Modular Enantioselective Approach to Construction of the Macrolactone Core of Polycavernoside A. The Journal of Organic Chemistry. 63: 7389-7398. PMID 11672388 DOI: 10.1021/Jo981083T |
0.653 |
|
1998 |
Paquette LA. Studies Directed to the Synthesis of the Antifungal Antibiotic Aleurodiscal. Enantioselective Construction of an Advanced β-d-Xyloside Congener Synthesis. 1998: 495-508. DOI: 10.1055/S-1998-5921 |
0.305 |
|
1998 |
Gobley O, Meunier P, Gautheron B, Gallucci JC, Erker G, Dahlmann M, Schloss JD, Paquette LA. Some Newexo,exo-Bis(isodicyclopentadienyl)titanium and -zirconium Dichloride Derivatives: Synthesis, Characterization, and Evaluation as Propene Polymerization Catalysts Organometallics. 17: 4897-4903. DOI: 10.1021/Om980542D |
0.792 |
|
1998 |
Tsui HC, Paquette LA. Reversible charge-accelerated oxy-cope rearrangements Journal of Organic Chemistry. 63: 9968-9977. DOI: 10.1021/Jo982002W |
0.311 |
|
1998 |
Paquette LA, Zeng Q, Tsui HC, Johnston JN. Stereochemical models for the enantiocontrolled construction of fully functionalized C rings via intramolecular aldolization in advanced precursors to paclitaxel Journal of Organic Chemistry. 63: 8491-8509. DOI: 10.1021/Jo981749J |
0.623 |
|
1998 |
Paquette LA, Wang H, Zeng Q, Shih T. Heteroatomic Modulation of Oxyanionic Cope Rearrangement Rates. Consequences on Competing Nucleophilic Cleavage of an Oxetane Ring in Precursors to Paclitaxel Journal of Organic Chemistry. 63: 6432-6433. DOI: 10.1021/Jo981059F |
0.353 |
|
1998 |
Paquette LA, Bolin DG, Stepanian M, Branan BM, Mallavadhani UV, Tae J, Eisenberg SWE, Rogers RD. Intramolecular Oxymercuration of Stereoisomeric Cyclohexyl-Belted Poly(spirotetrahydrofuranyl) Platforms Journal of the American Chemical Society. 120: 11603-11615. DOI: 10.1021/Ja981756P |
0.328 |
|
1998 |
Paquette LA, Dyck BP. Studies Directed toward the Total Synthesis of Cerorubenic Acid-III. 5. A Radical Cyclization Route Leading to the Methyl Ester of the Natural Isomer1 Journal of the American Chemical Society. 120: 5953-5960. DOI: 10.1021/Ja980691N |
0.411 |
|
1998 |
Paquette LA, Wang H, Su Z, Zhao M. Enantiospecific Total Synthesis of Natural (+)-Taxusin. 2. Functionalization of the A-Ring and Arrival at the Target Journal of the American Chemical Society. 120: 5213-5225. DOI: 10.1021/Ja980538T |
0.427 |
|
1998 |
Paquette LA, Zhao M. Enantiospecific Total Synthesis of Natural (+)-Taxusin. 1. Retrosynthesis, Advancement to Diastereomeric trans-Δ9,10-Tricyclic Olefinic Intermediates, and the Stereocontrol Attainable Because of Intrinsic Rotational Barriers Therein Journal of the American Chemical Society. 120: 5203-5212. DOI: 10.1021/Ja9805371 |
0.473 |
|
1998 |
Paquette LA, Collado I, Purdie M. Total Synthesis of Spinosyn A. 2. Degradation Studies Involving the Pure Factor and Its Complete Reconstitution Journal of the American Chemical Society. 120: 2553-2562. DOI: 10.1021/Ja974010K |
0.406 |
|
1998 |
Paquette LA, Gao Z, Ni Z, Smith GF. Total Synthesis of Spinosyn A. 1. Enantioselective Construction of a Key Tricyclic Intermediate by a Multiple Configurational Inversion Scheme Journal of the American Chemical Society. 120: 2543-2552. DOI: 10.1021/Ja974009L |
0.404 |
|
1997 |
Bernardelli P, Paquette LA. Stereoselective Indium-Promoted Allylation of gamma-Hydroxy-gamma-Lactones under Aqueous Conditions. The Neighboring Carboxyl Effect. The Journal of Organic Chemistry. 62: 8284-8285. PMID 11671959 DOI: 10.1021/Jo9716800 |
0.784 |
|
1997 |
Paquette LA, Mitzel TM, Isaac MB, Crasto CF, Schomer WW. Diastereoselection during 1,2-Addition of the Allylindium Reagent to alpha-Thia and alpha-Amino Aldehydes in Aqueous and Organic Solvents. The Journal of Organic Chemistry. 62: 4293-4301. PMID 11671749 DOI: 10.1021/Jo970274D |
0.781 |
|
1997 |
Morwick TM, Paquette LA. Combined Addition of Alkenyl and Allenic Anions to Squarate Esters. Direct Competition between Six-Ring and Eight-Ring Electrocyclization of 1,2,4,6,8-Cumulenic Pentaenes. The Journal of Organic Chemistry. 62: 627-635. PMID 11671456 DOI: 10.1021/Jo961945V |
0.415 |
|
1997 |
Paquette LA, Kuo LH, Hamme AT, Kreuzholz R, Doyon J. Sensitivity of Substitution to the Extent of Self-Immolative Chirality Transfer during Reaction Cascades Originating from Squarate Esters The Journal of Organic Chemistry. 62: 1730-1736. DOI: 10.1021/Jo962182E |
0.399 |
|
1997 |
Paquette LA, Kuo LH, Doyon J. Enhanced Channeling of the Squarate Cascade through the Dianionic Oxy-Cope Option. Oxy Substitution Markedly Augments Syn Delivery of the Second Alkenyllithium Journal of the American Chemical Society. 119: 3038-3047. DOI: 10.1021/Ja964140D |
0.337 |
|
1997 |
Paquette LA, Hamme AT, Kuo LH, Doyon J, Kreuzholz R. Probe of the Stereochemically Determining Step in Squarate Ester Cascades. Proof that Helical Equilibration within the Octatetraene Intermediate Is Responsible and Definition of Steric Control Elements Journal of the American Chemical Society. 119: 1242-1253. DOI: 10.1021/Ja9632163 |
0.4 |
|
1997 |
Paquette LA, Zuev D. A modular approach to marine macrolide construction. 1. An enantiocontrolled route to the C1–C12 (AB) spiroacetal sector Tetrahedron Letters. 38: 5115-5118. DOI: 10.1016/S0040-4039(97)01140-4 |
0.695 |
|
1996 |
Paquette LA, Mitzel TM. Comparative Diastereoselectivity Analysis of Crotylindium and 3-Bromoallylindium Additions to alpha-Oxy Aldehydes in Aqueous and Nonaqueous Solvent Systems. The Journal of Organic Chemistry. 61: 8799-8804. PMID 11667857 |
0.775 |
|
1996 |
Paquette LA, Stepanian M, Mallavadhani UV, Cutarelli TD, Lowinger TB, Klemeyer HJ. Definition of Several Control Elements Relevant to the Stereodefined Serial Elaboration of Belted Poly(spirotetrahydrofurans) Fitted with a Cyclohexane Core. The Journal of Organic Chemistry. 61: 7492-7507. PMID 11667680 DOI: 10.1021/Jo960962H |
0.349 |
|
1996 |
Paquette LA, Lowinger TB, Bolin DG, Branan BM. trans,anti,trans-Tetra(spirotetrahydrofuranyl)cyclohexane-1,2-dione. Stereocontrolled Synthesis and Definition of Its Susceptibility to Photoisomerization. The Journal of Organic Chemistry. 61: 7486-7491. PMID 11667679 DOI: 10.1021/Jo960961P |
0.367 |
|
1996 |
Paquette LA, Doussot P. New Transformations Involving Squarate Esters. Multi-Channel Rearrangement Options Available To 2-(Dimethoxy-Methyl)-1-Cycloalken-1-Yl Adducts‡ Research On Chemical Intermediates. 22: 767-780. DOI: 10.1163/156856796X00313 |
0.402 |
|
1996 |
Landmesser NG, Tsui H, King CR, Paquette LA. Regiocontrolled C-8 Acylation of Castanospermine Synthetic Communications. 26: 2213-2221. DOI: 10.1080/00397919608003581 |
0.39 |
|
1996 |
Sivik MR, Bauer W, Schleyer PvR, Paquette LA. (1S,2S,9R,10R)-Tetracyclo[8.2.1.02,9.03,7]trideca-3,6-dienyllithium. Tentative Evidence for a Quinternary Equilibrium Involving a Cyclopentadienide Ion Organometallics. 15: 5202-5208. DOI: 10.1021/Om960533+ |
0.33 |
|
1996 |
Paquette LA, Bzowej EI, Kreuzholz R. Optically Pure C2-Symmetric Transition Metal Complexes. Steric Consequences of Flanking the Cyclopentadienyl Anion with a Pair of Bridged Bicyclic Terpene-Derived Hydrocarbon Subunits Organometallics. 15: 4857-4862. DOI: 10.1021/Om960391J |
0.398 |
|
1996 |
Morwick TM, Paquette LA. Mapping The Chemical Reactivity Of Polyquinanes Produced By 2-Fold Addition Of Vinyl Anions To Squarate Esters. A Bicyclic Case Study Journal of Organic Chemistry. 61: 146-152. DOI: 10.1021/Jo9516751 |
0.416 |
|
1996 |
Wang TZ, Pinard E, Paquette LA. Asymmetric synthesis of the diterpenoid marine toxin (+)-acetoxycrenulide Journal of the American Chemical Society. 118: 1309-1318. DOI: 10.1021/Ja9533609 |
0.41 |
|
1996 |
Paquette LA, Doyon J, Lung Huang K. Sequenced reactions involving squarate esters. The first suggestion that helical equilibration within the advanced octatetraene intermediate is responsible for stereochemical control Tetrahedron Letters. 37: 3299-3302. DOI: 10.1016/0040-4039(96)00580-1 |
0.363 |
|
1996 |
Paquette LA, Kuo LH, Doyon J. Reaction cascades based on squarate esters. 1,3-Dioxolane as a chaperone functional group for lithium ions Tetrahedron. 52: 11625-11636. DOI: 10.1016/0040-4020(96)00644-8 |
0.359 |
|
1995 |
Paquette LA, Branan BM. Isomerizations of 1,7-Diheteradispiro[4.0.4.4]tetradeca-11,13-dienes in the Presence of Tetracyanoethylene Heterocycles. 40: 101. DOI: 10.3987/Com-94-S19 |
0.398 |
|
1995 |
Wilson PD, Friedrich D, Paquette LA. Successive electrocyclic rearrangements initiated by the addition of a lithiated cyclopropenone acetal to a squarate ester Journal of the Chemical Society, Chemical Communications. 1351-1352. DOI: 10.1039/C39950001351 |
0.417 |
|
1995 |
Mach K, Hiller J, Thewalt U, Sivik MR, Bzowej EI, Paquette LA, Zaegel F, Meunier P, Gautheron B. Stereoselective Redox Reaction Of Isodicyclopentadiene With The Bis(Tetrachloroaluminato)(Benzene)Titanium(Ii) Complex Organometallics. 14: 2609-2612. DOI: 10.1021/Om00005A072 |
0.328 |
|
1995 |
Paquette LA, Montgomery FJ, Wang T. An Abbreviated, Highly Stereocontrolled Route to Precursors of Taxol. Elaboration of a Fully Functionalized C Ring by Means of Intramolecular Aldol Cyclization Journal of Organic Chemistry. 60: 7857-7864. DOI: 10.1021/Jo00129A027 |
0.433 |
|
1995 |
Paquette LA, Bailey S. Evaluation of D-Ribose as an Enantiopure Building Block for Construction of the C-Ring of Taxol and Its Congeners The Journal of Organic Chemistry. 60: 7849-7856. DOI: 10.1021/Jo00129A026 |
0.321 |
|
1995 |
Paquette LA, Borrelly S. Studies Directed Toward The Total Synthesis Of Kalmanol. An Approach To Construction Of The C/D Diquinane Substructure Journal of Organic Chemistry. 60: 6912-6921. DOI: 10.1021/Jo00126A049 |
0.338 |
|
1995 |
Paquette LA, Hormuth S, Lovely CJ. Studies Directed toward the Total Synthesis of Cerorubenic Acid-III. 4. Exploration of an Organometallic Approach to Construction of the Eastern Sector Journal of Organic Chemistry. 60: 4813-4821. DOI: 10.1021/Jo00120A026 |
0.611 |
|
1995 |
Paquette LA, Su Z, Bailey S, Montgomery FJ. Evaluation of 2-Bromocyclohexenone Acetals as Vehicles for the Introduction of C-7 Oxygen Preliminary to the Synthesis of Taxane Diterpenes The Journal of Organic Chemistry. 60: 897-902. DOI: 10.1021/Jo00109A021 |
0.31 |
|
1995 |
Elmore SW, Paquette LA. Stereocontrolled Oxygenation of Camphor Derivatives as a Prelude to the Complete .beta.-Ring Functionalization of Potential Precursors to Taxol and Structural Analogs Thereof Journal of Organic Chemistry. 60: 889-896. DOI: 10.1021/Jo00109A020 |
0.322 |
|
1995 |
Detert H, Lanter JC, Paquette LA. Weiss-Cook Condensations Involving Unsaturated And Transannularly Alkylated Cyclododecane-1,2-Diones Journal of Organic Chemistry. 60: 353-356. DOI: 10.1021/Jo00107A013 |
0.383 |
|
1995 |
Lord MD, Negri JT, Paquette LA. Oxonium Ion-Initiated Pinacolic Ring Expansion Reactions. Application To The Enantioselective Synthesis Of The Spirocyclic Sesquiterpene Ethers Dactyl Oxene-B And -C Journal of Organic Chemistry. 60: 191-195. DOI: 10.1021/Jo00106A033 |
0.423 |
|
1995 |
Paquette LA, Morwick T. The Squarate Ester-1,3,5,7-Octatetraene-Polyquinane Cascade: Reaction Efficiency Is Intimately Linked to the Locus of Substitution within the Vinyl Anion Journal of the American Chemical Society. 117: 1451-1452. DOI: 10.1021/Ja00109A039 |
0.41 |
|
1994 |
Lin H, Paquette LA. A Convenient Method for Determining the Concentration of Grignard Reagents Synthetic Communications. 24: 2503-2506. DOI: 10.1080/00397919408010560 |
0.305 |
|
1994 |
Klemeyer HJ, Paquette LA. Consequences of .alpha.-Bromo Substitution on the Course of Allylmetal Additions to 1-Oxaspiro[4.5]dec-7-en-6-one Journal of Organic Chemistry. 59: 7924-7927. DOI: 10.1021/Jo00104A062 |
0.327 |
|
1994 |
Branan BM, Paquette LA. In Quest of Tricyclo[4.4.1.04,11]undeca-1,3,5,7,9-pentaene, a Highly Strained, Cyclic 10.pi.-Electron, Polyunsaturated Hydrocarbon. Synthesis of a Methoxyl-Substituted Dihydro Derivative Journal of Organic Chemistry. 59: 7709-7713. DOI: 10.1021/Jo00104A029 |
0.33 |
|
1994 |
Paquette LA, Wang X. Total Synthesis of 18-Oxo-3-virgene, a Constituent of the Waxy Surface Resins of Tobacco The Journal of Organic Chemistry. 59: 2052-2057. DOI: 10.1021/Jo00087A019 |
0.368 |
|
1994 |
Houk KN, Li Y, McAllister MA, O'Doherty G, Paquette LA, Siebrand W, Smedarchina ZK. Mechanistic Analysis of Double Hydrogen Dyotropy in syn-Sesquinorbornene Disulfones. A Combined Kinetic and Theoretical Evaluation of Primary Deuterium Isotope Effects Journal of the American Chemical Society. 116: 10895-10913. DOI: 10.1021/Ja00103A005 |
0.528 |
|
1994 |
O'Doherty GA, Rogers RD, Paquette LA. Consequences of Modulated Precompression along Reaction Coordinates. Synthesis, Crystallographic Structural Studies, and Rate of Intramolecular Dyotropy in an Extended Series of syn-Sesquinorbornene Disulfones Journal of the American Chemical Society. 116: 10883-10894. DOI: 10.1021/Ja00103A004 |
0.604 |
|
1994 |
Williams JP, St. Laurent DR, Friedrich D, Pinard E, Roden BA, Paquette LA. Total synthesis of the Lycopodium alkaloids magellanine and magellaninone by three-fold annulation of 2-cyclopentenone Journal of the American Chemical Society. 116: 4689-4696. DOI: 10.1021/Ja00090A017 |
0.356 |
|
1993 |
Paquette LA, Deaton DN, Endo Y, Poupart MA. Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization The Journal of Organic Chemistry. 58: 4262-4273. DOI: 10.1021/Jo00068A021 |
0.411 |
|
1993 |
Paquette LA, Lassalle GY, Lovely CJ. Studies directed toward the total synthesis of cerorubenic acid-III. 2. Analysis of the inability to realize D ring formation by means of extraannular Robinson annulation Journal of Organic Chemistry. 58: 4254-4261. DOI: 10.1021/Jo00068A020 |
0.662 |
|
1993 |
Paquette LA, Poupart MA. Studies directed toward the total synthesis of cerorubenic acid-III. 1. Expedient construction of the tetracyclic core by oxyanionic sigmatropy Journal of Organic Chemistry. 58: 4245-4253. DOI: 10.1021/Jo00068A019 |
0.442 |
|
1993 |
Paquette LA, Astles PC. Total synthesis of furanocembranolides. 3. A concise convergent route to acerosolide Journal of Organic Chemistry. 58: 165-169. DOI: 10.1021/Jo00053A031 |
0.35 |
|
1993 |
Negri J, Morwick T, Doyon J, Wilson PD, Hickey ER, Paquette LA. Direct elaboration of complex polyquinanes through twofold addition of vinyl anions to squarate esters Journal of the American Chemical Society. 115: 12189-12190. DOI: 10.1021/Ja00078A077 |
0.326 |
|
1993 |
Paquette LA, Wang TZ, Huu VN. Access to naturally occurring cyclooctanoids by two-carbon intercalation. Total synthesis of (+)-ceroplastol I Journal of the American Chemical Society. 115: 1676-1683. DOI: 10.1021/Ja00058A011 |
0.349 |
|
1993 |
Gallucci JC, Opromolla G, Paquette LA, Pardi L, Schirch PFT, Sivik MR, Zanello P. Redox behavior of ferrocene derivatives. 2. Bis(.eta.5-tricyclo[5.2.1.02,6]deca-2,5,8-trien-6-yl)iron and related molecules Inorganic Chemistry. 32: 2292-2297. DOI: 10.1021/Ic00063A018 |
0.333 |
|
1993 |
Guevel R, Paquette LA. An enzyme-based synthesis of (S)-(−)-3-methyl-2-[(phenylsiilfonyl)-methyl]butyl phenyl sulfide and the stereochemical course of its alkylation Tetrahedron-Asymmetry. 4: 947-956. DOI: 10.1016/S0957-4166(00)80137-8 |
0.364 |
|
1993 |
Paquette LA, Ting-Zhong W, Wang S, Philippo CMG. Enantioselective synthesis of (+)-cleomeolide, the structurally unique diterpene lactone constituent of Cleome viscosa Tetrahedron Letters. 34: 3523-3526. DOI: 10.1016/S0040-4039(00)73626-4 |
0.384 |
|
1993 |
Rogers RD, Sivik MR, Paquette LA. Isodicyclopentadienes and related molecules Journal of Organometallic Chemistry. 450: 125-135. DOI: 10.1016/0022-328X(93)80148-5 |
0.353 |
|
1992 |
Liang S, Paquette LA. Palladium-catalyzed intramolecular cyclization of vinyl and aryl triflates. Associated regioselectivity of the beta-hydride elimination step. Acta Chemica Scandinavica (Copenhagen, Denmark : 1989). 46: 597-605. PMID 1419434 |
0.314 |
|
1992 |
Ladouceur G, Paquette LA. Application of the anionic oxy-cope rearrangement to stereocontrolled synthesis of the A/B subunit of cytoxic 8,9-seco-ent-kaurenes Synthesis. 1992: 185-191. DOI: 10.1055/S-1992-34185 |
0.375 |
|
1992 |
Paquette LA, Sivik MR. Isodicyclopentadienes and related molecules. 57. Stereocontrolled synthesis of sterically crowded titanocenes of high enantiomeric purity by electrophilic capture of C-silylated ligands with configurational inversion Organometallics. 11: 3503-3505. DOI: 10.1021/Om00059A009 |
0.367 |
|
1992 |
Paquette LA, Maleczka RE. Enantioselective construction of natural (+)-pallescensin A. A sigmatropic pathway to furanosesquiterpenes Journal of Organic Chemistry. 57: 7118-7122. DOI: 10.1021/Jo00052A026 |
0.685 |
|
1992 |
Brown DS, Paquette LA. Synthetic studies on furanoheliangolides. Stereocontrolled construction of the oxygen-bridged tricyclic framework The Journal of Organic Chemistry. 57: 4512-4521. DOI: 10.1021/Jo00042A036 |
0.338 |
|
1992 |
Paquette LA, Andrews JFP, Vanucci C, Lawhorn DE, Negri JT, Rogers RD. Regio- and stereochemical course of the ring expansion of bridged bicyclic ketones to spirocyclic .alpha.-keto tetrahydrofurans. The Journal of Organic Chemistry. 57: 3956-3965. DOI: 10.1021/Jo00040A042 |
0.383 |
|
1992 |
Paquette LA, Underiner TL, Gallucci JC. Structural analysis of cis-[n.3.1]bicyclic ketones by x-ray crystallography. Impact of the observed conformational crossover by .pi.-facially diastereoselective nucleophilic additions to this class of ketones and on the stereochemical course of electrophilic reactions involving their methylene analogs Journal of Organic Chemistry. 57: 86-96. DOI: 10.1021/Jo00027A018 |
0.355 |
|
1992 |
Gree D, Gree R, Lowinger TB, Martelli J, Negri JT, Paquette LA. Acid-catalyzed cyclization of 1,4-diols tethered to (butadiene)iron tricarbonyl segments. Isotopic labeling as a mechanistic probe of stereochemical retention during tetrahydrofuran formation Journal of the American Chemical Society. 114: 8841-8846. DOI: 10.1021/Ja00049A015 |
0.333 |
|
1992 |
Paquette LA, Sauer DR, Cleary DG, Kinsella MA, Blackwell CM, Anderson LG. Application of palladium-catalyzed [3 + 2] cycloaddition technology to the elaboration of kempane diterpenes. Stereocontrolled synthesis of (.+-.)-3.alpha.-hydroxy-7.beta.-kemp-8(9)-en-6-one and (.+-.)-3.beta.-hydroxykemp-7(8)-en-6-one Journal of the American Chemical Society. 114: 7375-7387. DOI: 10.1021/Ja00045A007 |
0.313 |
|
1992 |
Rayner CM, Astles PC, Paquette LA. Total synthesis of furanocembranolides. 2. Macrocyclization studies culminating in the synthesis of a dihydropseudopterolide and gorgiacerone. Related furanocembranolide interconversions. Journal of the American Chemical Society. 114: 3926-3936. DOI: 10.1021/Ja00036A046 |
0.405 |
|
1992 |
Paquette LA, Doherty AM, Rayner CM. Total synthesis of furanocembranolides. 1. Stereocontrolled preparation of key heterocyclic building blocks and assembly of a complete seco-pseudopterane framework Journal of the American Chemical Society. 114: 3910-3926. DOI: 10.1021/Ja00036A045 |
0.392 |
|
1992 |
Paquette LA, Zhao M, Friedrich D. An unprecedented silyl triflate-promoted hydride shift within a taxane derivative Tetrahedron Letters. 33: 7311-7314. DOI: 10.1016/S0040-4039(00)60174-0 |
0.409 |
|
1992 |
Paquette LA, Branan BM, Rogers RD. X-ray crystallographic study of α-brominated diketo teraquinanes. Conformational effects of the number of halogens and their position on bond length and solit-state conformation Tetrahedron. 48: 297-306. DOI: 10.1016/S0040-4020(01)88141-2 |
0.339 |
|
1992 |
Graham RJ, Paquette LA. A Diepoxide Belonging to the Rare C1Point Group Journal of the Chinese Chemical Society. 39: 279-283. DOI: 10.1002/Jccs.199200049 |
0.355 |
|
1992 |
Paquette LA, Combrink KD, Elmore SW, Zhao M. Setting the Bridgehead Oxidation Level intrans-Tricyclo[9.3.1.03,8]pentadecanes as a Prelude to the Dual Synthesis of Taxol and Taxusin Helvetica Chimica Acta. 75: 1772-1791. DOI: 10.1002/hlca.19920750604 |
0.645 |
|
1991 |
Sornay C, Meunier P, Gautheron B, O'Doherty GA, Paquette LA. Isodicyclopentadienes and related molecules. Part 54. Stereoselective access to the three diisodicyclopentadienyltitanium dichlorides Organometallics. 10: 2082-2083. DOI: 10.1021/Om00052A068 |
0.568 |
|
1991 |
Maleczka RE, Paquette LA. Adaptation of oxyanionic sigmatropy to the convergent enantioselective synthesis of ambergris-type odorants The Journal of Organic Chemistry. 56: 6538-6546. DOI: 10.1021/Jo00023A018 |
0.606 |
|
1991 |
Paquette LA, Dahnke K, Doyon J, He W, Wyant K, Friedrich D. Regioselective conversion of cycloalkanones to vinyl bromides with 1,2-functionality transposition. A general stratagem Journal of Organic Chemistry. 56: 6199-6205. DOI: 10.1021/Jo00021A044 |
0.307 |
|
1991 |
Friedrich D, Paquette LA. Cyclopentenyllithium additions to chiral aldehydes. Diastereofacial selectivity indicating the absence of a pronounced neighboring carboxylate anion effect Journal of Organic Chemistry. 56: 3831-3840. DOI: 10.1021/Jo00012A013 |
0.412 |
|
1991 |
Paquette LA, Maleczka RE, Qiu FY. Regio- and stereoselective oxidation of unsaturated bicyclo[2.2.2]octanones with selenium dioxide The Journal of Organic Chemistry. 56: 2455-2461. DOI: 10.1021/Jo00007A037 |
0.646 |
|
1991 |
Paquette LA, Maleczka RE. Enantioselective Total Synthesis Of (-)-9-Epi-Ambrox, A Potent Ambergris-Type Olfactory Agent Journal of Organic Chemistry. 56: 912-913. DOI: 10.1021/Jo00003A004 |
0.62 |
|
1991 |
Paquette LA, O'Doherty GA, Rogers RD. Intramolecular reaction rate is not determined exclusively by the distance separating reaction centers. The kinetic consequences of modulated ground state strain on dyotropic hydrogen migration in systems of very similar geometric disposition [Erratum to document cited in CA115(17):182353r] Journal of the American Chemical Society. 113: 9710-9710. DOI: 10.1021/Ja00025A067 |
0.561 |
|
1991 |
Paquette LA, O'Doherty GA, Rogers RD. Intramolecular reaction rate is not determined exclusively by the distance separating reaction centers. The kinetic consequences of modulated ground state strain on dyotropic hydrogen migration in systems of very similar geometric disposition Journal of the American Chemical Society. 113: 7761-7762. DOI: 10.1021/Ja00020A048 |
0.569 |
|
1991 |
Bauer W, O'Doherty GA, Schleyer PvR, Paquette LA. Isodicyclopentadienes and related molecules. 58. Structural analysis of a camphor-derived cyclopentadienyllithium compound by NMR and MNDO. A ternary equilibrium in tetrahydrofuran Journal of the American Chemical Society. 113: 7093-7100. DOI: 10.1021/Ja00019A001 |
0.538 |
|
1991 |
Philippo CMG, Huu VN, Paquette LA. Two-carbon intercalation. 4-Cyclooctenones by tandem application of double-Tebbe and Claisen reactions Journal of the American Chemical Society. 113: 2762-2764. DOI: 10.1021/Ja00007A066 |
0.305 |
|
1991 |
Gugelchuk M, Paquette LA. Isodicyclopentadienes and related molecules. 54. Remote electronic perturbation of .pi.-facial stereoselectivity in [4+2] cycloadditions to isodicyclopentafulvenes. The consequences of p-phenyl substitution Journal of the American Chemical Society. 113: 246-253. DOI: 10.1021/Ja00001A035 |
0.36 |
|
1991 |
Elmore SW, Combrink KD, Paquette LA. A convenient means for controlling the oxidation level of bridgehead carbon C-1 in functionalized tricyclo[9.3.1.03,8]pentadecanes Tetrahedron Letters. 32: 6679-6682. DOI: 10.1016/S0040-4039(00)93573-1 |
0.672 |
|
1990 |
Paquette LA, Fristad WE. Oxidation chemistry of a cis-2-(3-flurylidene)ethanol Heterocycles. 31: 2219-2224. DOI: 10.3987/Com-90-5597 |
0.338 |
|
1990 |
Paquette LA, Lawhorn DE, Teleha CA. Response of 2-lithio-4,5-dihydrofuran : ketone adducts to acid catalysis Heterocycles. 30: 765-769. DOI: 10.3987/Com-89-S87 |
0.37 |
|
1990 |
Paquette LA, Ra CS, Edmonson SD. Regiocontrolled cyclohexenone annulation via acylation of a ketone carbonyl Journal of Organic Chemistry. 55: 2443-2445. DOI: 10.1021/Jo00295A037 |
0.425 |
|
1990 |
Paquette LA, Sweeney TJ. A concise total synthesis of enantiomerically pure (+)-cis- and (+)-trans-lauthisan Journal of Organic Chemistry. 55: 1703-1704. DOI: 10.1021/Jo00293A006 |
0.38 |
|
1990 |
Paquette LA, Ross RJ, Shi YJ. Regioselective routes to nucleophilic optically active 2- and 3-carene systems Journal of Organic Chemistry. 55: 1589-1598. DOI: 10.1021/Jo00292A039 |
0.511 |
|
1990 |
Paquette LA, Macdonald D, Anderson LG. Total synthesis of (+)-ikarugamycin. 2. Elaboration of the macrocyclic lactam and tetramic acid substructures and complete assembly of the antibiotic Journal of the American Chemical Society. 112: 9292-9299. DOI: 10.1021/Ja00181A035 |
0.438 |
|
1990 |
Paquette LA, Romine JL, Lin HS, Wright J. Total synthesis of (+)-ikarugamycin. 1. Stereocontrolled construction of the decahydro-as-indacene subunit Journal of the American Chemical Society. 112: 9284-9292. DOI: 10.1021/Ja00181A034 |
0.341 |
|
1990 |
Paquette LA, Bauer W, Sivik MR, Buehl M, Feigel M, Schleyer PvR. Structure of lithium isodicyclopentadienide and lithium cyclopentadienide in tetrahydrofuran solution. A combined NMR, IGLO, and MNDO study Journal of the American Chemical Society. 112: 8776-8789. DOI: 10.1021/Ja00180A020 |
0.317 |
|
1990 |
Paquette LA, Rayner CM, Doherty AM. Synthesis of (.+-.)-11,0(3)-dihydropseudopterolide Journal of the American Chemical Society. 112: 4078-4079. DOI: 10.1021/Ja00166A077 |
0.372 |
|
1990 |
Paquette LA, Shen CC. Isodicyclopentadienes and related molecules. 49. Synthesis, static structure, and kinetic stability of a syn-sesquinorbornatriene Journal of the American Chemical Society. 112: 1159-1164. DOI: 10.1021/Ja00159A041 |
0.311 |
|
1990 |
Paquette LA, Wang TZ, Luo J, Cottrell CE, Clough AE, Anderson LB. Is pseudorotation the operational pathway for bond shifting within [8]annulenes? Probe of planarization requirements by 1,3-annulation of the cyclooctatetraene ring. Kinetic analysis of racemization and 2-D NMR quantitation of .pi.-bond alternation and ring inversion as a function of polymethylene chain length Journal of the American Chemical Society. 112: 239-253. DOI: 10.1021/Ja00157A038 |
0.353 |
|
1990 |
Liang S, Paquette LA. Biocatalytic-based synthesis of optically pure (C-6)-functionalized 1-(tert-butyldimethylsilyloxy) 2-methyl-(E)-2-heptenes Tetrahedron-Asymmetry. 1: 445-452. DOI: 10.1016/S0957-4166(00)86349-1 |
0.347 |
|
1990 |
Ezquerra J, He W, Paquette LA. Enantiospecific synthesis of the the tricyclxc nucleus of acetoxycrenulide by claisen ring exfansion Tetrahedron Letters. 31: 6979-6982. DOI: 10.1016/S0040-4039(00)97221-6 |
0.396 |
|
1990 |
Paquette LA, Sweeney TJ. Stereospecific approach to 3-oxocen-7-ones via aliphatic claisen rearrangement. synthesis of (+)-(2R,8S)- and (+)-(2R,8J)-lauthisan Tetrahedron. 46: 4487-4502. DOI: 10.1016/S0040-4020(01)85577-0 |
0.387 |
|
1990 |
Paquette LA. Stereocontrolled Construction of Complex Cyclic Ketones via Oxy‐Cope Rearrangement Angewandte Chemie. 29: 609-626. DOI: 10.1002/Anie.199006091 |
0.425 |
|
1989 |
Gallucci JC, Taylor RT, Kobayashi T, Weber JC, Krause J, Paquette LA. X-ray crystallographic analysis of the structural distortions induced by substitution and annulation of the dodecahedrane nucleus Acta Crystallographica, Section C: Crystal Structure Communications. 45. PMID 2610983 DOI: 10.1107/S0108270188013721 |
0.309 |
|
1989 |
Paquette LA, O'Doherty GA, Miller BL, Rogers RD, Rheingold AL, Geib SL. Isodicyclopentadienes and related molecules. 48. Stereochemically uniform mode of iron carbonyl complexation to spirocyclic isodicyclopentadienes Organometallics. 8: 2167-2172. DOI: 10.1021/Om00111A012 |
0.507 |
|
1989 |
Paquette LA, Shi YJ. Stereocontrolled construction of hydroazulenones by sequential anionic oxy-Cope rearrangement - SN' allylic ether displacement Journal of Organic Chemistry. 54: 5205-5207. DOI: 10.1021/Jo00283A007 |
0.366 |
|
1989 |
Paquette LA, Galatsis P. Functional group manipulation along the perimeter of a hemispherical molecule. Synthesis of dihydro- and tetrahydro-C16-hexaquinacene The Journal of Organic Chemistry. 54: 5039-5043. DOI: 10.1021/Jo00282A018 |
0.309 |
|
1989 |
Paquette LA, DeRussy DT, Pegg NA, Taylor RT, Zydowsky TM. Direct oxygenation of enolates generated by anionic oxy-Cope rearrangement. Expedient preparation of polycyclic .alpha.-hydroxy ketones Journal of Organic Chemistry. 54: 4576-4581. DOI: 10.1021/Jo00280A023 |
0.35 |
|
1989 |
Cheney DL, Paquette LA. Studies directed toward the total synthesis of trixikingolide. Analysis of the capacity for transannular carbon-carbon bond formation in various bicyclic and tricyclic intermediates Journal of Organic Chemistry. 54: 3334-3347. DOI: 10.1021/Jo00275A018 |
0.326 |
|
1989 |
Paquette LA, Maynard GD, Ra CS, Hoppe M. Cleavage of carbon-carbon bonds with high stereochemical control. 7. Chiral .alpha.-silyl benzoylcycloalkanes undergo base-catalyzed cleavage with retention of configuration when not sterically congested Journal of Organic Chemistry. 54: 1408-1418. DOI: 10.1021/Jo00267A032 |
0.343 |
|
1989 |
Gilday JP, Gallucci JC, Paquette LA. Cleavage of carbon-carbon bonds with high stereochemical control. 6. Asymmetric synthesis of chiral C-centered organosilanes by Haller-Bauer cleavage of optically active, nonenolizable .alpha.-silyl phenyl ketones Journal of Organic Chemistry. 54: 1399-1408. DOI: 10.1021/Jo00267A031 |
0.376 |
|
1989 |
Paquette LA, Macdonald D, Anderson LG, Wright J. A triply convergent enantioselective total synthesis of (+)-ikarugamycin Journal of the American Chemical Society. 111: 8037-8039. DOI: 10.1021/Ja00202A067 |
0.371 |
|
1989 |
Paquette LA, Reagan J, Schreiber SL, Teleha CA. Intramolecular SN' cleavage of allylic ethers by enolate anions Journal of the American Chemical Society. 111: 2331-2332. DOI: 10.1021/Ja00188A073 |
0.536 |
|
1989 |
Paquette LA, Choon SR, Silvestri TW. Free radical cyclization approach to a functionalized [3] peristylane Tetrahedron. 45: 3099-3106. DOI: 10.1016/S0040-4020(01)80136-8 |
0.456 |
|
1989 |
Paquette LA, Oplinger JA. Limitations in the application of anionic oxy-cope sigmatropy to elaboration of the forskolin nucleus Tetrahedron. 45: 107-124. DOI: 10.1016/0040-4020(89)80038-9 |
0.388 |
|
1989 |
Gugelchuk M, Paquette LA. Can Electron Transmission from Aza-Crown Ethers Contribute to Diels-Alder π-Facial Selectivity? Israel Journal of Chemistry. 29: 165-169. DOI: 10.1002/Ijch.198900024 |
0.35 |
|
1988 |
Weber JC, Paquette LA. Synthesis of amino-substituted dodecahedranes, secododecahedranes, and homododecahedranes, and their antiviral relationship to 1-aminoadamantane The Journal of Organic Chemistry. 53: 5315-5320. DOI: 10.1021/Jo00257A021 |
0.339 |
|
1988 |
Paquette LA, Ra CS. Cleavage of carbon-carbon bonds with high stereochemical control. 5. Course of the Haller-Bauer reaction of cyclic .alpha.-phenyl ketones Journal of Organic Chemistry. 53: 4978-4985. DOI: 10.1021/Jo00256A014 |
0.35 |
|
1988 |
Paquette LA, Gugelchuk M. Modulation of .pi.-facial selectivity in Diels-Alder cycloaddition to isodicyclopentafulvenes by remote para substitution of an exocyclic phenyl group The Journal of Organic Chemistry. 53: 1835-1837. DOI: 10.1021/Jo00243A054 |
0.313 |
|
1988 |
Paquette LA, Pansegrau PD, Wiedeman PE, Springer JP. (+)-Pleuromutilin synthetic studies. Examples of intramolecular hydrogen abstraction by the .beta.-carbon of a 2-cyclopentenone subunit with resultant .alpha.-coupling Journal of Organic Chemistry. 53: 1461-1466. DOI: 10.1021/Jo00242A021 |
0.322 |
|
1988 |
Paquette LA, Bulman-Page PC, Pansegrau PD, Wiedeman PE. (+)-Pleuromutilin synthetic studies. Direct degradation to and independent preparation of an advanced diketone intermediate. Demonstration that reconstruction of the eight-membered ring suffers from serious kinetic retardation Journal of Organic Chemistry. 53: 1450-1460. DOI: 10.1021/Jo00242A020 |
0.347 |
|
1988 |
Paquette LA, Okazaki ME, Caille JC. A formal total synthesis of (.+-.)-laurenene Journal of Organic Chemistry. 53: 477-481. DOI: 10.1021/Jo00238A003 |
0.362 |
|
1988 |
Wright J, Drtina GJ, Roberts RA, Paquette LA. A convergent synthesis of triquinane sesterterpenes. Enantioselective synthesis of (-)-retigeranic acid A Journal of the American Chemical Society. 110: 5806-5817. DOI: 10.1021/Ja00225A036 |
0.365 |
|
1988 |
Paquette LA, Wang TZ. The first cyclooctatetraene to which bond shifting is more accessible than ring inversion Journal of the American Chemical Society. 110: 3663-3665. DOI: 10.1021/Ja00219A054 |
0.336 |
|
1988 |
Paquette LA, Kobayashi T, Gallucci JC. Cyclopropanation of spherical hydrocarbons without need for prior olefination. The synthesis of cyclopropadodecahedranes Journal of the American Chemical Society. 110: 1305-1307. DOI: 10.1021/Ja00212A057 |
0.371 |
|
1988 |
Gilday JP, Paquette LA. Stabilized carbanions by alkyllithium-induced decarboxylation of non-enolizable carboxylic acids. An anionic equivalent to the hunsdiecker reaction Tetrahedron Letters. 29: 4505-4508. DOI: 10.1016/S0040-4039(00)80532-8 |
0.375 |
|
1988 |
Paquette LA, Shen C. Extended functionalized of the fluted [4]peristylane perimeter Tetrahedron Letters. 29: 4069-4072. DOI: 10.1016/S0040-4039(00)80419-0 |
0.318 |
|
1988 |
Paquette LA, Poupart M. Rapid construction of the tetracyclic nucleus of cerorubenic acid-III by oxyanionic cope chemistry Tetrahedron Letters. 29: 273-276. DOI: 10.1016/S0040-4039(00)80072-6 |
0.31 |
|
1988 |
Poupart M, Paquette LA. Conformational consequences of intramolecular cyclopropanation within small bicyclic systems. Synthesis and desymmetrization of 1-methyltricyclo[2.2.2.02,6]octane-3,5-dione Tetrahedron Letters. 29: 269-272. DOI: 10.1016/S0040-4039(00)80071-4 |
0.322 |
|
1988 |
Blankenship C, Wells GJ, Paquette LA. Desilylative condensation reactions of electronegatively substituted 1-(trimethylsilyl)cyclopropanes1 Tetrahedron. 44: 4023-4032. DOI: 10.1016/S0040-4020(01)86653-9 |
0.396 |
|
1988 |
Paquette LA, DeRussy DT, Rogers RD. On possible redirection of the course of anionic oxy-cope rearrangements Tetrahedron. 44: 3139-3148. DOI: 10.1016/S0040-4020(01)85945-7 |
0.33 |
|
1987 |
Paquette LA, Learn KS, Romine JL. Double Diastereoselection Operative During π-Facially Selective Addition of Chiral 1-Cyclopentenyllithium Reagents to (7R)-7-Methyl-7-Vinylbicyclo[3.2.0]Hept-2-En-6-One Synthetic Communications. 17: 369-375. DOI: 10.1080/00397918708063913 |
0.353 |
|
1987 |
Cleary DG, Paquette LA. Cycloaddition of the Trimethylenemethane-Palladium Complex to Activated Six-Membered and Medium-Ring Enones Synthetic Communications. 17: 497-501. DOI: 10.1080/00397918708056435 |
0.353 |
|
1987 |
Paquette LA, Burke LD. Triplet-state benzonorbornadiene di-.pi.-methane photorearrangements. Competition between bridgehead and vinyl substituents for control of the product-determining 1,2-aryl shift step Journal of Organic Chemistry. 52: 2674-2679. DOI: 10.1021/Jo00389A008 |
0.31 |
|
1987 |
Paquette LA, Miyahara Y. Directed alkyl substitution of the dodecahedrane nucleus. The 1,4-dimethyl, 1,6-dimethyl, and 1,4,16-trimethyl derivatives. Indanododecahedrane by stepwise dehydrogenation of a benzylated seco derivative Journal of Organic Chemistry. 52: 1265-1272. DOI: 10.1021/Jo00383A017 |
0.383 |
|
1987 |
Paquette L, Fristad W, Dime D, Bailey T. Additions and Corrections - Silanes in Organic Synthesis. 8. Preparation of Vinylsilanes from Ketones and Their Regiospecific Cyclopentenone Annulation. Journal of Organic Chemistry. 52: 1176-1176. DOI: 10.1021/Jo00382A600 |
0.364 |
|
1987 |
Ross RJ, Paquette LA. Ingenane synthetic studies. Stereocontrolled introduction of all oxygenated and unsaturated centers in an ingenol prototype Journal of Organic Chemistry. 52: 5497-5498. DOI: 10.1021/Jo00233A048 |
0.517 |
|
1987 |
Paquette LA, Gugelchuk M, McLaughlin ML. Isodicyclopentadienes and related molecules. 38. Homochiral pinene-fused cyclopentadienes. Synthesis and .pi.-facially selective course of Diels-Alder cycloadditions and metallocene formation The Journal of Organic Chemistry. 52: 4732-4740. DOI: 10.1021/Jo00230A015 |
0.561 |
|
1987 |
Paquette LA, Gilday JP, Ra CS. Haller-Bauer cleavage of open-chain and cyclic .alpha.-phenyl ketones proceeds with retention of configuration Journal of the American Chemical Society. 109: 6858-6860. DOI: 10.1021/Ja00256A054 |
0.334 |
|
1987 |
Paquette LA, Pierre F, Cottrell CE. Anionic rearrangements of syn- and anti-7-cyclopentenyl-7-hydroxynorbornenes. The case for sequential ring cleavage and intramolecular Michael addition Journal of the American Chemical Society. 109: 5731-5740. DOI: 10.1021/Ja00253A027 |
0.373 |
|
1987 |
Waykole L, Paquette LA. Synthesis of [4.4.4]propellahexaene Journal of the American Chemical Society. 109: 3174-3175. DOI: 10.1021/Ja00244A067 |
0.372 |
|
1987 |
Paquette LA, Ham WH. Total synthesis of the marine sesquiterpenes dactylol and africanol. De novo construction of a cyclooctanoid natural product from cycloheptane precursors Journal of the American Chemical Society. 109: 3025-3036. DOI: 10.1021/Ja00244A026 |
0.34 |
|
1987 |
Dressel J, Paquette LA. Tricyclo[5.3.0.02,8]deca-3,5,9-triene Journal of the American Chemical Society. 109: 2857-2858. DOI: 10.1021/Ja00243A067 |
0.332 |
|
1987 |
Oplinger JA, Paquette LA. Synthesis of the forskolin skeleton via anionic oxy-cope rearrangement Tetrahedron Letters. 28: 5441-5444. DOI: 10.1016/S0040-4039(00)96749-2 |
0.36 |
|
1987 |
Paquette LA, Lin H, Coghlan MJ. Total synthesis of (±)-sterpuric acid Tetrahedron Letters. 28: 5017-5020. DOI: 10.1016/S0040-4039(00)96684-X |
0.319 |
|
1987 |
Paquette LA, Trova MP. Belting of the cyclooctatetraene ring across the transannular 1- and 5-positions Tetrahedron Letters. 28: 2795-2798. DOI: 10.1016/S0040-4039(00)96211-7 |
0.381 |
|
1987 |
Paquette LA, Romine JL, Lin H. Diastereoselective π-facially controlled nucleophilic additions of chiral vinylorganometallics to chiral β,γ-unsaturated ketones. 2. A practical method for stereocontrolled elaboration of the decahydro--indacene subunit of ikarugamycin Tetrahedron Letters. 28: 31-34. DOI: 10.1016/S0040-4039(00)95641-7 |
0.346 |
|
1987 |
Paquette LA, Schaefer AG, Springer JP. Synthesis of (±)-14-epiupial by manganese(III) -γ-lactone annulation Tetrahedron. 43: 5567-5582. DOI: 10.1016/S0040-4020(01)87738-3 |
0.437 |
|
1987 |
Paquette LA, Learn KS, Romine JL. Doubly diastereoselective nucleophilic additions to a bicyclic β,γ-unsaturated ketone possessing a conformationally mobile double bond Tetrahedron. 43: 4989-5002. DOI: 10.1016/S0040-4020(01)87678-X |
0.428 |
|
1987 |
MCLAUGHLIN ML, MCKINNEY JA, PAQUETTE LA. ChemInform Abstract: Efficient Preparation of Homochiral Bicyclo-Annulated Cyclopentadienes via the Skattebol Rearrangement. Avoidance of Limitations due to Angle Strain. Part 36. Cheminform. 18. DOI: 10.1002/chin.198721142 |
0.468 |
|
1986 |
Paquette LA, Learn KS. .pi.-Facially controlled nucleophilic additions of chiral vinylorganometallics to chiral .beta.,.gamma.-unsaturated ketones. 1. Double diastereoselection studies involving 7,7-dimethoxy-5-norbornen-2-one Journal of the American Chemical Society. 108: 7873-7875. PMID 22283323 DOI: 10.1021/Ja00284A085 |
0.32 |
|
1986 |
Paquette LA, Lau CJ. Kinetic and Thermodynamic Control of Aldolization in Higher Order Polyquinane Systems Synthetic Communications. 16: 103-110. DOI: 10.1080/00397918608057696 |
0.32 |
|
1986 |
Wang TZ, Paquette LA. Photochemical route to a representative 1,8-annulated 7-methylene-1,3,5-cyclooctatriene Journal of Organic Chemistry. 51: 5232-5234. DOI: 10.1021/Jo00376A034 |
0.344 |
|
1986 |
St. Laurent DR, Paquette LA. Cyclopentannulation with a 1,3-dicarbonyl dipole equivalent. Synthesis of bicyclo[3.3.0]oct-1(5)-ene-2,6-dione The Journal of Organic Chemistry. 51: 3861-3864. DOI: 10.1021/Jo00370A021 |
0.37 |
|
1986 |
Paquette LA, Coghlan MJ, Cottrell CE, Irie T, Tanida H. Regioselectivity of pyridine ring migration during triplet-sensitized di-.pi.-methane photorearrangements of 5,8-dihydro-5,8-methanoisoquinoline derivatives. The case for heteroatom control The Journal of Organic Chemistry. 51: 696-699. DOI: 10.1021/Jo00355A020 |
0.337 |
|
1986 |
Paquette LA, Kunzer H. Photoinitiated quadricyclane-quadricyclane rearrangements Journal of the American Chemical Society. 108: 7431-7433. DOI: 10.1021/Ja00283A061 |
0.317 |
|
1986 |
Jendralla H, Jelich K, DeLucca G, Paquette LA. Functionalized polyunsaturated [4.4.4]propellanes. Synthesis, intraring chemistry, and backbone rearrangements. [4.4.4]propella-2,4,7,9,12-pentaene and its thermal frangibility Journal of the American Chemical Society. 108: 3731-3739. DOI: 10.1021/Ja00273A030 |
0.311 |
|
1986 |
Paquette LA, Kuenzer H, Green KE, De Lucchi O, Licini G, Pasquato L, Valle G. Consequences of fixing three parallel coplanar double bonds in close proximity with different geometries. Synthesis and spectral parameters of syn- and anti-sesquinorbornatriene Journal of the American Chemical Society. 108: 3453-3460. DOI: 10.1021/Ja00272A047 |
0.304 |
|
1986 |
Paquette LA, McKinney JA, McLaughlin ML, Rheingold AL. Transition metal complexation of optically pure annulated cyclopentadies. Face selectivity, three-dimensional structural features, and utilization for asymmetric hydrogenation Tetrahedron Letters. 27: 5599-5602. DOI: 10.1016/S0040-4039(00)85275-2 |
0.471 |
|
1986 |
McLaughlin ML, McKinney JA, Paquette LA. Efficient preparation of homochiral bicyclo-annulated cyclopentadienes via the skattebøl rearrangement. Avoidance of limitations due to angle strain Tetrahedron Letters. 27: 5595-5598. DOI: 10.1016/S0040-4039(00)85274-0 |
0.515 |
|
1986 |
Paquette LA, Ham WH. Total synthesis of africanol Tetrahedron Letters. 27: 2341-2344. DOI: 10.1016/S0040-4039(00)84524-4 |
0.399 |
|
1986 |
Paquette LA, Kravetz TM, Charumilind P. The 1,7-cyclohexenonorbornadiene system Tetrahedron. 42: 1789-1795. DOI: 10.1016/S0040-4020(01)87596-7 |
0.431 |
|
1986 |
Jendralla H, Jelich K, Delucca G, Paquette LA. Functionalized Polyunsaturated [4.4.4]Propellanes. Synthesis, Intraring Chemistry, and Backbone Rearrangements. Cheminform. 17. DOI: 10.1002/Chin.198642165 |
0.364 |
|
1986 |
Paquette LA, Coghlan MJ, Cottrell CE, Irie T, Tanida H. Regioselectivity of Pyridine Ring Migration During Triplet-Sensitized Di-n-methane Photorearrangements of 5,8-Dihydro-5,8-methanoisoquinoline Derivatives. Cheminform. 17. DOI: 10.1002/Chin.198636116 |
0.357 |
|
1986 |
Hill RK, Morton GH, Peterson JR, Walsh JA, Paquette LA. Synthesis and Chiroptical Properties of 5,7-Dioxobicyclo[2.2.2]oct-2-ene and Bicyclo[2.2.2]octane-2,5-dione. Cheminform. 17. DOI: 10.1002/Chin.198627163 |
0.351 |
|
1986 |
Paquette LA, Nakamura K, Engel P. Synthesis of hexacyclo[5.4.1.02,6.03,10.04,8.09,12]dodecane‐5,11‐dione and its conversion to di‐, tri‐, and tetranitro‐1,3‐bishomopentaprismanes Chemische Berichte. 119: 3782-3800. DOI: 10.1002/Cber.19861191222 |
0.366 |
|
1985 |
Haraldsson GG, Paquette LA, Springer JP. Stereoselective epoxidation of a 5,6,6-trisubstituted cyclohex-2-enone Journal of the Chemical Society, Chemical Communications. 1035-1036. DOI: 10.1039/C39850001035 |
0.309 |
|
1985 |
Hill RK, Morton GH, Peterson JR, Walsh JA, Paquette LA. Synthesis and chiroptical properties of 5,7-dioxobicyclo[2.2.2]oct-2-ene and bicyclo[2.2.2]octane-2,5-dione Journal of Organic Chemistry. 50: 5528-5533. DOI: 10.1021/Jo00350A019 |
0.331 |
|
1985 |
Paquette LA, Peterson JR, Ross RJ. Migratory selectivity in the ring expansion of .alpha.,.beta.-unsaturated cyclic ketones via .beta.-hydroxy selenides Journal of Organic Chemistry. 50: 5200-5204. DOI: 10.1021/Jo00225A043 |
0.542 |
|
1985 |
Paquette LA, Belmont DT, Asu YL. Regiospecific and stereoselective alkylation of the octahydronaphthal-8(9)-en-3-one nucleus Journal of Organic Chemistry. 50: 4667-4672. DOI: 10.1021/Jo00224A001 |
0.321 |
|
1985 |
Paquette LA, Hathaway SJ, Schirch PFT. Electronic control of stereoselectivity. 29. Stereochemical and regiochemical course of isodicyclopentadiene-tropone cycloaddition reactions The Journal of Organic Chemistry. 50: 4199-4205. DOI: 10.1021/Jo00222A005 |
0.304 |
|
1985 |
Barth W, Paquette LA. Synthesis of a representative cis/trans pair of 4,5-disubstituted cyclopentenyllithium reagents Journal of Organic Chemistry. 50: 2438-2443. DOI: 10.1021/Jo00214A008 |
0.318 |
|
1985 |
Galemmo RA, Paquette LA. Contrasting directed-Aldol reactivity of a pair of epimeric trimethylsilyl enol ethers The Journal of Organic Chemistry. 50: 1768-1770. DOI: 10.1021/Jo00210A045 |
0.355 |
|
1985 |
Kinney WA, Coghlan MJ, Paquette LA. General approach to annulated 4-cyclooctenones by aliphatic Claisen rearrangement. Stereospecific total synthesis of (.+-.)-precapnelladiene Journal of the American Chemical Society. 107: 7352-7360. DOI: 10.1021/Ja00311A023 |
0.366 |
|
1985 |
Paquette LA, Kravetz TM, Hsu LY. Electronic control of stereoselectivity. 31. .pi.-Facial course of Diels-Alder cycloadditions to 10-isopropylideneisodicyclopentadiene Journal of the American Chemical Society. 107: 6598-6603. DOI: 10.1021/Ja00309A029 |
0.306 |
|
1985 |
Paquette LA, Kuenzer H, Green KE. syn-Sesquinorbornatriene and its quadricyclane valence isomer Journal of the American Chemical Society. 107: 4788-4790. DOI: 10.1021/Ja00302A036 |
0.306 |
|
1985 |
Paquette LA, Ham WH, Dime DS. A formal total synthesis of dactylol Tetrahedron Letters. 26: 4983-4986. DOI: 10.1016/S0040-4039(01)80832-7 |
0.429 |
|
1985 |
Paquette LA, Wiedeman PE, Bulman-Page PC. A relay approach to (+)-pleuromutilin. III. direct degradation of the natural product to the key diketone intermediate and its chemospecific functionalization Tetrahedron Letters. 26: 1611-1614. DOI: 10.1016/S0040-4039(00)98565-4 |
0.313 |
|
1985 |
Paquette LA, Bulman-Page PC. A relay approach to (+)-pleuromutilin. II. preparation of an advanced optically pure intermediate Tetrahedron Letters. 26: 1607-1610. DOI: 10.1016/S0040-4039(00)98564-2 |
0.305 |
|
1985 |
Paquette LA, Wiedeman PE. A relay to (+)-pleuromutilin. I. synthesis of a levorotatory tricyclic lactone subunit Tetrahedron Letters. 26: 1603-1606. DOI: 10.1016/S0040-4039(00)98563-0 |
0.31 |
|
1985 |
Paquette LA, Nakamura K, Fischer JW. Synthesis of a versatile functionalized tetraquinane. Convenient access to 1,3-bishomopentaprismanedione Tetrahedron Letters. 26: 4051-4054. DOI: 10.1016/S0040-4039(00)89290-4 |
0.402 |
|
1985 |
Hathaway SJ, Paquette LA. Electronic control of stereoselectivity-21. Stereochemical parallelism between dienophilic capture and singlet oxygenation of isodicyclopentadiene derivatives1 1 Part 20:Y.-L. Hsu, S.J. Hathaway and L.A. Paquette, Tetrahedron Lett. 259(1984) Tetrahedron. 41: 2037-2043. DOI: 10.1016/S0040-4020(01)96574-3 |
0.328 |
|
1985 |
Haraldsson GG, Paquette LA, Springer JP. Stereoselective Epoxidation Of A 5,6,6-Trisubstituted Cyclohex-2-Enone Cheminform. 16. DOI: 10.1002/Chin.198548165 |
0.452 |
|
1985 |
Kinney WA, Coghlan MJ, Paquette LA. Claisen Rearrangement Of 6-Alkenyl-2-Methylenetetrahydropyrans. A New Approach To Annulated 4-Cyclooctenones And A Stereospecific Synthesis O Precapnelladiene Cheminform. 16. DOI: 10.1002/Chin.198508307 |
0.31 |
|
1985 |
Paquette LA, Roberts RA, Drtina GJ. Total Synthesis Of (-)-Silphiperfol-6-Ene And (-)-5-Oxosilphiperfol-6-Ene Cheminform. 16. DOI: 10.1002/Chin.198508306 |
0.368 |
|
1985 |
Paquette LA, Blankenship C, Wells GJ. Silicon In Organic Synthesis. 27. A Method For The Generation Of Electronegatively Substituted Cyclopropyl Anions Under Preparatively Useful Conditions. Aldol Condensation With Carbonyl Partners Cheminform. 16. DOI: 10.1002/Chin.198506140 |
0.37 |
|
1985 |
PAQUETTE LA, HSU L, GALLLUCCI JC, KORP JD, BERNAL I, KRAVETZ TM, HATHAWAY SJ. ChemInform Abstract: Electronic Control of Stereoselectivity. Part 24. Interrelationship of π-Bond Tilting and the Stereochemical Disposition of Substituents at C-2 and C-7 within Norbornyl-Fused 4-Cycloheptenones. Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198502058 |
0.322 |
|
1984 |
Paquette LA, Stevens KE. Stereocontrolled total synthesis of the triquinane marine sesquiterpene Δ9(12)-capnellene Canadian Journal of Chemistry. 62: 2415-2420. DOI: 10.1139/V84-415 |
0.372 |
|
1984 |
Blankenship C, Paquette LA. Double Hunsdiecker Reactions. Convenient Preparation of 1,1-Dibromocyclopropane and 1,1-Dibromocyclobutane Synthetic Communications. 14: 983-987. DOI: 10.1080/00397918408059624 |
0.415 |
|
1984 |
Paquette LA, Daniels RG, Gleiter R. Silanes in organic synthesis. 24. Synthesis, reactivity, and electronic structure of [2-(trimethylsilyl)-1,3-cyclohexadiene]iron tricarbonyl complexes Organometallics. 3: 560-567. DOI: 10.1021/Om00082A009 |
0.305 |
|
1984 |
Paquette LA, Green KE, Gleiter R, Schaefer W, Gallucci JC. Electronic control of stereoselectivity. 27. The effect of apical spirocyclopropane substitution on the stereochemical course of Diels-Alder cycloadditions to norbornyl-fused diene systems Journal of the American Chemical Society. 106: 8232-8240. DOI: 10.1021/Ja00338A037 |
0.328 |
|
1984 |
Kinney WA, Coghlan MJ, Paquette LA. Claisen rearrangement of 6-alkenyl-2-methylenetetrahydropyrans. A new approach to annulated 4-cyclooctenones and a stereospecific synthesis of precapnelladiene Journal of the American Chemical Society. 106: 6868-6870. DOI: 10.1021/Ja00334A081 |
0.354 |
|
1984 |
Paquette LA, Roberts RA, Drtina GJ. Total synthesis of (−)-silphiperfol-6-ene and ()-5-oxosilphiperfol-6-ene Journal of the American Chemical Society. 106: 6690-6693. DOI: 10.1021/Ja00334A038 |
0.305 |
|
1984 |
Paquette LA, Blankenship C, Wells GJ. Silicon in organic synthesis. 27. A method for the generation of electronegatively substituted cyclopropyl anions under preparatively useful conditions. Aldol condensation with carbonyl partners Journal of the American Chemical Society. 106: 6442-6443. DOI: 10.1021/Ja00333A068 |
0.349 |
|
1984 |
Paquette LA, Hsu LY, Gallucci JC, Korp JD, Bernal I, Kravetz TM, Hathaway SJ. Interrelationship of .pi.-bond tilting and the stereochemical disposition of substituents at C-2 and C-7 within norbornyl-fused 4-cycloheptenones Journal of the American Chemical Society. 106: 5743-5744. DOI: 10.1021/Ja00331A063 |
0.303 |
|
1984 |
Paquette LA, Nitz TJ, Ross RJ, Springer JP. Ingenane synthetic studies. An expedient approach to highly oxygenated ABC subunits of ingenol via reductive dialkylative annulation and .alpha.,.beta.-epoxy ketone photoisomerization Journal of the American Chemical Society. 106: 1446-1454. DOI: 10.1021/Ja00317A043 |
0.539 |
|
1984 |
Paquette LA, Hathaway SJ, Gallucci JC. Selective trapping of rearranged spirocyclic isodicyclopentadienes by tropone Tetrahedron Letters. 25: 2659-2662. DOI: 10.1016/S0040-4039(01)81256-9 |
0.364 |
|
1984 |
Hsu LY, Hathaway SJ, Paquette LA. Electronic control of stereoselectivity. 20. Crystal and molecular structure of the ferrocene derived from tricyclo[5.2.1.02,6]Deca-2,5,8-triene Tetrahedron Letters. 25: 259-262. DOI: 10.1016/S0040-4039(00)99855-1 |
0.304 |
|
1984 |
Charumilind P, Paquette LA. Electronic control of stereoselectivity. 26. On the inability of fused cyclopropane rings to direct the stereochemical course of dienophile capture by tetracyclo[5.3.2.02,6.08,10]dodeca-2,5,11-triene and its dihydro derivative Journal of the American Chemical Society. 106: 8225-8232. DOI: 10.1002/Chin.198517089 |
0.344 |
|
1984 |
Wells GJ, Yan TH, Paquette LA. Silicon in organic synthesis. 24. Preparation and selected reactions of functionalized 1-(trimethylsilyl)-substituted cyclopropanes The Journal of Organic Chemistry. 49: 3604-3609. DOI: 10.1002/Chin.198509281 |
0.364 |
|
1984 |
Paquette LA, Valpey RS, Annis GD. SILICON IN ORGANIC SYNTHESIS. 23. CHLORO((TRIMETHYLSILYL)METHYL)KETENE AS A USEFUL INTERMEDIATE FOR THE ELABORATION OF α-METHYLENECYCLOBUTANONES AND -CYCLOPENTANONES Cheminform. 15. DOI: 10.1002/Chin.198435177 |
0.33 |
|
1984 |
Carr RVC, Williams RV, Paquette LA. Dienophilic Properties Of Phenyl Vinyl Sulfone And Trans-1-(Phenylsulfonyl)-2-(Trimethylsilyl)Ethylene. Their Utilization As Synthons For Ethylene, 1-Alkenes, Acetylene, And Monosubstituted Alkynes In The Construction Of Functionalize Cheminform. 15. DOI: 10.1002/Chin.198426094 |
0.367 |
|
1984 |
Paquette LA, Gardlik JM, Mccullough KJ, Samodral R, Delucca G, Ouellette RJ. Bond Fixation In Annulenes. 16. Synthesis Of The 1,2-Dimethyl-3-Phenylcyclooctatetraene ⇄ 1,8-Dimethyl-2-Phenylcyclooctatetraene Bond Shift Isomer Pair. Probe Of The Relative Size Of A Flanking Phenyl Substituent By Means Of Racemizat Cheminform. 15. DOI: 10.1002/Chin.198414173 |
0.346 |
|
1984 |
Paquette LA, Annis GD. Total Synthesis Of (.+-.)-Pentalenene, The Least Oxidized Neutral Triquinane Metabolite Of Streptomyces Griseochromogenes Cheminform. 15. DOI: 10.1002/Chin.198412314 |
0.302 |
|
1983 |
Carr RVC, Williams RV, Paquette LA. Dienophilic properties of phenyl vinyl sulfone and trans-1-(phenylsulfonyl)-2-(trimethylsilyl)ethylene. Their utilization as synthons for ethylene, 1-alkenes, acetylene, and monosubstituted alkynes in the construction of functionalized six-membered rings via [4 + 2] .pi. cycloaddition methodology Journal of Organic Chemistry. 48: 4976-4986. DOI: 10.1021/Jo00173A039 |
0.417 |
|
1983 |
Hathaway SJ, Paquette LA. Silanes in organic synthesis. 19. Examination of (-)-.alpha.-naphthylphenylmethylallylsilane as a template for effecting chirality transfer from silicon to carbon The Journal of Organic Chemistry. 48: 3351-3353. DOI: 10.1021/Jo00167A047 |
0.304 |
|
1983 |
Roberts RA, Schuell V, Paquette LA. Electrophile-initiated ring-opening reactions of 2-methylene-6,6-dimethylbicyclo[3.1.0]hexanes. New methodology for the synthesis of highly functionalized 1,2,3-trisubstituted cyclopentenes Journal of Organic Chemistry. 14: 2076-2084. DOI: 10.1021/Jo00160A028 |
0.452 |
|
1983 |
Paquette LA, Gardlik JM, McCullough KJ, Samodral R, DeLucca G, Ouellette RJ. Bond fixation in annulenes. 16. Synthesis of the 1,2-dimethyl-3-phenylcyclooctatetraene .dblarw. 1,8-dimethyl-2-phenylcyclooctatetraene bond shift isomer pair. Probe of the relative size of a flanking phenyl substituent by means of racemization kinetics Journal of the American Chemical Society. 105: 7649-7655. DOI: 10.1021/Ja00364A031 |
0.358 |
|
1983 |
Paquette LA, Charumilind P, Gallucci JC. Silanes in organic synthesis. 20. Regio- and stereochemical definition of silatropic migration within trimethylsilyl-substituted isodicyclopentadienes Journal of the American Chemical Society. 105: 7364-7375. DOI: 10.1021/Ja00363A026 |
0.337 |
|
1983 |
Paquette LA, Galemmo RA, Springer JP. Synthesis of the alleged structure of senoxydene, the triquinane sesquiterpene derived from Senecio oxyodontus Journal of the American Chemical Society. 105: 6975-6976. DOI: 10.1021/Ja00361A046 |
0.326 |
|
1983 |
Browne AR, Kearney FR, Mason SF, Paquette LA, Drake AF. Electronic absorption and circular dichroism spectra of the perturbed coplanar cis-diene chromophore in deuterium- and methyl-substituted 7,7-dimethylbicyclo[4.1.1]octa-2,4-dienes Journal of the American Chemical Society. 105: 6123-6129. DOI: 10.1021/Ja00357A025 |
0.348 |
|
1983 |
Paquette LA, Browne AR, Doecke CW, Williams RV. Short, stereocontrolled synthesis of [4]peristylane Journal of the American Chemical Society. 105: 4113-4115. DOI: 10.1021/Ja00350A072 |
0.332 |
|
1983 |
Paquette LA, Wells GJ, Horn KA, Yan TH. Silicon in organic synthesis-17. Cyclopentannulation by thermolysis of (1-trimethylsilylcyclopropyl)ethylenes-the 1-trimethylsilylcyclopropyl anion1 1 Part 16. T.-H. Yan and L.A. Paquette, Tetrahedron Letters 3227 (1982) Tetrahedron. 39: 913-924. DOI: 10.1016/S0040-4020(01)88590-2 |
0.427 |
|
1983 |
Paquette LA, Balogh DW, Ternansky RJ, Begley WJ, Banwell MG. Dissolving-metal reduction of a hemispherical dichloro diester. Tests of relative enolate nucleophilicity within a mixed dianion and oxidative behavior of a trisecododecahedryl alcohol The Journal of Organic Chemistry. 48: 3282-3288. DOI: 10.1002/Chin.198407183 |
0.356 |
|
1982 |
Paquette LA. Ring inversion and bond shifting energetics in substituted chiral cyclooctatetraenes Pure and Applied Chemistry. 54: 987-1004. DOI: 10.1351/Pac198254050987 |
0.368 |
|
1982 |
Daniels RG, Paquette LA. Silanes in organic synthesis. 18. Preparation and reactivity of optically active vinyl- and dienylsilanes Organometallics. 14: 1449-1453. DOI: 10.1021/Om00071A007 |
0.301 |
|
1982 |
Paquette LA, Daniels RG. Silanes in organic synthesis. 15. Silicon-directed hydride abstraction from [2-(trimethylsilyl)-1,3-cyclohexadiene]iron tricarbonyl complexes and nucleophilic addition to the derived cations Organometallics. 1: 757-760. DOI: 10.1021/Om00065A018 |
0.326 |
|
1982 |
Paquette LA, Klinger F. Electronic control of stereoselectivity. 11. Long-range modulation of stereoselection in Diels-Alder cycloadditions of N-methyltriazolinedione to aryl-substituted 9-allylidenebenzonorbornenes The Journal of Organic Chemistry. 47: 272-275. DOI: 10.1021/Jo00341A017 |
0.316 |
|
1982 |
Leone-Bay A, Paquette LA. Total synthesis of racemic silphinene Journal of Organic Chemistry. 14: 4173-4174. DOI: 10.1021/Jo00142A037 |
0.367 |
|
1982 |
Annis GD, Paquette LA. Total synthesis of (.+-.)-pentalenene Journal of the American Chemical Society. 104: 4504-4506. DOI: 10.1021/Ja00380A041 |
0.357 |
|
1982 |
Paquette LA, Ternansky RJ, Balogh DW. A strategy for the synthesis of monosubstituted dodecahedrane and the isolation of an isododecahedrane Journal of the American Chemical Society. 104: 4502-4503. DOI: 10.1021/Ja00380A039 |
0.304 |
|
1982 |
Paquette LA, Crouse GD, Sharma AK. Relationship of the anionic behavior of unsaturated medium-ring alcohols to structure. Generation and antarafacial cyclization of coiled 8.pi.-electron carbanions Journal of the American Chemical Society. 104: 4411-4423. DOI: 10.1021/Ja00380A016 |
0.301 |
|
1982 |
Paquette LA, Balogh DW. An Expedient Synthesis Of 1,16-Dimethyldodecahedrane Journal of the American Chemical Society. 104: 774-783. DOI: 10.1021/Ja00367A021 |
0.374 |
|
1982 |
Tu-Hsin Y, Paquette LA. Silicon in organic synthesis. 16. A short synthesis of (+±)-α-vetispirene Tetrahedron Letters. 23: 3227-3230. DOI: 10.1016/S0040-4039(00)87576-0 |
0.33 |
|
1982 |
Paquette LA, Wells GJ, Horn KA, Yan TH. Silicon in organic synthesis. 14. Five ring annulation processes based upon thermal rearrangement of (1-trimethylsilylcyclopropyl)ethylenes Tetrahedron Letters. 23: 263-266. DOI: 10.1016/S0040-4039(00)86804-5 |
0.415 |
|
1982 |
Paquette LA, Horn KA, Wells GJ. Silicon in organic syntheis. 13. The 1-trimethylsilylcyclopropyl anion and its formal equivalent Tetrahedron Letters. 23: 259-262. DOI: 10.1016/S0040-4039(00)86803-3 |
0.38 |
|
1982 |
Paquette LA, Kinney WA. A new synthon for the regiospecific γ-alkylation of 2-cyclohexenones. Application to the synthesis of zingiberenol and oxygenated bicycle[3.3.1] nonanes Tetrahedron Letters. 23: 131-134. DOI: 10.1016/S0040-4039(00)86766-0 |
0.334 |
|
1982 |
Paquette LA, Kinney WA. A vinyl sulfone-mediated diels-alder approach to the fully regiocontrolled elaboration of 4,5-disubstituted 2- and 3-cyclohexenones Tetrahedron Letters. 23: 5127-5130. DOI: 10.1016/S0040-4039(00)85776-7 |
0.338 |
|
1982 |
Hanzawa Y, Paquette L. Photochemical Preparation Of 5-Tert-Butyl-4-Methoxycarbonyltetracyclo(3.3.0.02,4.03,6)Oct-7-Ene Synthesis. 1982: 661-662. DOI: 10.1002/Chin.198301116 |
0.345 |
|
1981 |
Crouse GD, Paquette LA. Total synthesis of (.+-.)-multifidene, the gamete attractant of the phaeophyte Cutleria multifida Journal of Organic Chemistry. 13: 4272-4274. DOI: 10.1021/Jo00334A034 |
0.361 |
|
1981 |
Klobucar WD, Paquette LA, Blount JF. Synthesis of and absolute configurational assignment to enantiomerically pure unsaturated [4.4.2]propellanes Journal of Organic Chemistry. 13: 4021-4030. DOI: 10.1021/Jo00333A017 |
0.403 |
|
1981 |
Daniels RG, Paquette LA. Silanes in organic synthesis. 10. Cleavage reactions of silylcyclopropanes with titanium tetrachloride and hydrogen chloride Journal of Organic Chemistry. 12: 2901-2910. DOI: 10.1021/Jo00327A013 |
0.366 |
|
1981 |
Pfeil JL, Kukolja S, Paquette LA. Azetidinone antibiotics. 20. Synthesis of 7.beta.-amido-7.alpha.-methoxy-3-methyl-1-oxacephalosporin The Journal of Organic Chemistry. 46: 827-829. DOI: 10.1021/Jo00317A043 |
0.301 |
|
1981 |
Paquette LA, Crouse GD. Mild base-promoted conversion of tertiary cis,cis-2,4-cyclononadienols to bicyclo[4.3.1]nona-2,4-dienes. Antarafacial cyclization of coiled 8.pi.-7C conjugated anions Journal of the American Chemical Society. 103: 6235-6236. DOI: 10.1021/Ja00410A052 |
0.311 |
|
1981 |
Bohm M, Carr R, Gleiter R, Paquette L. Additions and Corrections - Electronic Control of Stereoselectivity. 4. Effects of Neighboring Fused Bicyclic Frameworks on the Stereochemical Outcome of Diels-Alder Cycloadditions to Cyclopentadiene Rings Journal of the American Chemical Society. 103: 2910-2910. DOI: 10.1021/Ja00400A604 |
0.329 |
|
1981 |
Hanzawa Y, Paquette LA. Bond fixation in annulenes. 12. Effect of vicinal di-tert-butyl substitution on cyclooctatetraene valence isomerization. 7,8-Di-tert-butylbicyclo[4.2.0]octa-2,4,7-triene Journal of the American Chemical Society. 103: 2269-2272. DOI: 10.1021/Ja00399A022 |
0.353 |
|
1981 |
Paquette LA, Han Y. Total synthesis of (.+-.)-isocomene, a naturally occurring triquinane Journal of the American Chemical Society. 103: 1835-1838. DOI: 10.1021/Ja00397A044 |
0.354 |
|
1981 |
Daniels RG, Paquette LA. Silanes in organic syuthesis. 11. Regiocontrolled synthesis of α-hydroxymethylated (trimethylsilyl)allenes☆ Tetrahedron Letters. 22: 1579-1582. DOI: 10.1016/S0040-4039(01)90382-X |
0.369 |
|
1981 |
Paquette LA, Williams RV. Silicon in organic synthesis. 12. trans-1-benzenesulfonyl-2-(trimethylsilyl)ethylene, a Diels-Alder dienophile equivalent of acetylene and monosubstituted acetylenes Tetrahedron Letters. 22: 4643-4646. DOI: 10.1016/S0040-4039(01)83002-1 |
0.388 |
|
1981 |
Stevens KE, Paquette LA. Stereocontrolled total synthesis of (±)-Δ9(12)-capnellene Tetrahedron Letters. 22: 4393-4396. DOI: 10.1016/S0040-4039(01)82965-8 |
0.315 |
|
1981 |
Crouse GD, Paquette LA. Relative kinetic ordering of [1,3]-hydrogen migration, anionic oxy-cope rearrangement, and base-accelerated dehydration in tertiary cyclononatrienyl alkoxides Tetrahedron Letters. 22: 3167-3170. DOI: 10.1016/S0040-4039(01)81854-2 |
0.337 |
|
1981 |
Paquette LA, Vazeux M. Threefold transannular epoxide cyclization. Synthesis of a heterocyclic C17-hexaquinane Tetrahedron Letters. 22: 291-294. DOI: 10.1016/0040-4039(81)80078-0 |
0.415 |
|
1981 |
Schostarez H, Paquette LA. Highly stereocontrolled synthesis of [3.3.3] propellane sesquiterpenes. ( ± )-Modhephene and (±)-epimodhephene Tetrahedron. 37: 4431-4435. DOI: 10.1016/0040-4020(81)80009-9 |
0.366 |
|
1981 |
Paquette LA, Doehner RFJ. Synthesis Of Optically Active Triazolinediones And Examination Of Their Utility For Inducing Asymmetry In Diels-Alder Cycloaddition Reactions Cheminform. 12. DOI: 10.1002/Chin.198115239 |
0.354 |
|
1980 |
Matsumoto K, Ikemi-Kono Y, Uchida T, Paquette LA. Synthesis and Cycloaddition Reactions of 3-Cyanoindolizines Heterocycles. 14: 103. DOI: 10.3987/R-1980-01-0103 |
0.399 |
|
1980 |
Fristad W, Bailey T, Paquette L. Additions and Corrections - Silanes in Organic Synthesis. 9. Enesilylation as a Method for 1,2-Carbonyl Migration within Ketones and for the Conversion to 1,2-Transposed Allylic Alcohols. Journal of Organic Chemistry. 45: 5434-5434. DOI: 10.1021/Jo01314A625 |
0.306 |
|
1980 |
Park H, Paquette LA. Synthesis of the C2v- and S4-symmetric tetraesters of tricyclo[3.3.0.03,7]octane Journal of Organic Chemistry. 12: 5378-5379. DOI: 10.1021/Jo01314A037 |
0.304 |
|
1980 |
Paquette LA, Doehner RF. Synthesis of optically active triazolinediones and examination of their utility for inducing asymmetry in Diels-Alder cycloaddition reactions Journal of Organic Chemistry. 45: 5105-5113. DOI: 10.1021/Jo01313A018 |
0.354 |
|
1980 |
Paquette LA, Carr RVC, Arnold E, Clardy J. Electronic control of stereoselectivity. 5. Stereochemistry of singlet oxygen capture by cyclopentadiene rings fused to norbornyl and norbornenyl frameworks The Journal of Organic Chemistry. 45: 4907-4913. DOI: 10.1021/Jo01312A018 |
0.304 |
|
1980 |
Paquette LA, Fristad WE, Dime DS, Bailey TR. Silanes in organic synthesis. 8. Preparation of vinylsilanes from ketones and their regiospecific cyclopentenone annulation Journal of Organic Chemistry. 11: 3017-3028. DOI: 10.1021/Jo01303A020 |
0.338 |
|
1980 |
Boehm MC, Carr RVC, Gleiter R, Paquette LA. Electronic control of stereoselectivity. 4. Effects of neighboring fused bicyclic frameworks on the stereochemical outcome of Diels-Alder cycloadditions to cyclopentadiene rings Journal of the American Chemical Society. 102: 7218-7228. DOI: 10.1021/Ja00544A008 |
0.323 |
|
1980 |
Gree R, Park H, Paquette LA. Regio- and stereoselective 1,2 Wagner-Meerwein shifts during trifluoroacetic acid catalyzed isomerization of unsymmetrically substituted tricyclo[3.2.0.02,4]heptanes Journal of the American Chemical Society. 102: 4397-4403. DOI: 10.1021/Ja00533A018 |
0.371 |
|
1980 |
Paquette LA, Crouse GD, Sharma AK. A stereocontrolled synthetic entry to the primary prostaglandins from butadiene. Oxy anionic substituent effects on [1,5]-hydrogen sigmatropy Journal of the American Chemical Society. 102: 3972-3974. DOI: 10.1021/Ja00531A060 |
0.305 |
|
1980 |
Jenkins JA, Doehner RE, Paquette LA. Synthesis and absolute configuration of 4,5-diazatwist-4-ene Journal of the American Chemical Society. 102: 2131-2133. DOI: 10.1021/Ja00526A082 |
0.389 |
|
1980 |
Paquette LA, Carr RVC, Boehm MC, Gleiter R. Electronic control of stereoselectivity. 3. Stereoselection operative in [4 + 2].pi. cycloadditions to cyclopentadiene rings fused at C2,C3 to bicyclic frameworks Journal of the American Chemical Society. 102: 1186-1188. DOI: 10.1021/Ja00523A058 |
0.338 |
|
1980 |
Ohkata K, Paquette LA. Geometric dependence to long-range interaction of fused cyclopropane rings in tris-.sigma.-homotropylium cations Journal of the American Chemical Society. 102: 1082-1092. DOI: 10.1021/Ja00523A027 |
0.309 |
|
1980 |
Paquette LA, Browne AR, Chamot E, Blount JF. Silver(I) catalyzed rearrangements of strained .sigma. bonds. 39. Twofold cyclopropylidene carbon-hydrogen insertion as a route to hexacyclic bis(bicyclo[1.1.0]butanes) and their silver(I) ion promoted rearrangement. A direct synthesis of heptalene from naphthalene Journal of the American Chemical Society. 102: 643-651. DOI: 10.1021/Ja00522A034 |
0.341 |
|
1980 |
Paquette LA, Chamot E, Browne AR. Silver(I) catalyzed rearrangements of strained .sigma. bonds. 38. Regiospecificity of cyclopropylidene carbon-hydrogen insertion reactions within [m.n.1]propellane frameworks Journal of the American Chemical Society. 102: 637-643. DOI: 10.1021/Ja00522A033 |
0.318 |
|
1980 |
Ohkata K, Doecke CW, Klein G, Paquette LA. Stereoelectronic effects on cyclobutyl participation. The 10-tetracyclo[5.2.1.02,6.O3,9]decyl cation Tetrahedron Letters. 21: 3253-3256. DOI: 10.1016/S0040-4039(00)78660-6 |
0.32 |
|
1980 |
Jenkins JA, Doehner REJ, Paquette LA. Synthesis and absolute configuration of 4,5-diazatwist-4-ene Cheminform. 11. DOI: 10.1002/Chin.198025236 |
0.389 |
|
1980 |
Paquette LA, Browne AR, Chamot E, Blount JF. Silver(I) Ion Catalyzed Rearrangements of Strained σ Bonds. Part 39. Twofold Cyclo-propylidene C-H Insertion as a Route to Hexacyclic Bis(bicyclo[1.1.0]butanes and Their Silver(I) Ion Promoted Rearrangement. A Direct Synthesis of Hept Cheminform. 11. DOI: 10.1002/Chin.198017122 |
0.344 |
|
1980 |
Paquette LA, Chamot E, Browne AR. Silver(I) Catalyzed Rearrangements Of Strained Σ Bonds. 38. Regiospecificity Of Cyclopropylidene Carbon‐Hydrogen Insertion Reactions Within (M.N.1)Propellane Frameworks Cheminform. 11. DOI: 10.1002/Chin.198017121 |
0.32 |
|
1980 |
Ku AY, Paquette LA, Rozeboom MD, Houk KN. Polar Effects On Di-Π-Methane Rearrangements. Regiospecificity In The Triplet-Sensitized Photoisomerizations Of 2-Cyanobenzonorbornadienes Carrying Methoxy Aryl Substituents Cheminform. 11. DOI: 10.1002/Chin.198003145 |
0.33 |
|
1979 |
Matsumoto K, Uchida T, Paquette LA. Synthesis of 3-Cyanoindolizines via Cycloaddition-Extrusion Reactions of Dicyanomethylids with Phenyl Vinyl Sulfoxide Synthesis. 1979: 746-747. DOI: 10.1055/S-1979-28826 |
0.396 |
|
1979 |
Paquette LA, Wyvratt MJ, Schallner O, Muthard JL, Begley WJ, Blankenship RM, Balogh D. Topologically spherical molecules. Synthesis of a pair of C2-symmetric hexaquinane dilactones and insights into their chemical reactivity. An efficient .pi.-mediated 1,6-dicarbonyl reduction Cheminform. 11: 3616-3630. DOI: 10.1021/Jo01335A003 |
0.336 |
|
1979 |
Ku AY, Paquette LA, Rozeboom MD, Houk KN. Polar effects on di-.pi.-methane rearrangements. Regiospecificity in the triplet-sensitized photoisomerizations of 2-cyanobenzonorbornadienes carrying methoxy aryl substituents Journal of the American Chemical Society. 101: 5981-5985. DOI: 10.1021/Ja00514A018 |
0.302 |
|
1979 |
Paquette LA, Ku AY, Santiago C, Rozeboom MD, Houk KN. Control of regioselectivity in the di-.pi.-methane rearrangements. Triplet-sensitized photoisomerization of benzonorbornadienes carrying cyano substituents in the aryl and vinyl segments Journal of the American Chemical Society. 101: 5972-5980. DOI: 10.1021/Ja00514A017 |
0.319 |
|
1979 |
Paquette LA, Fristad WE, Schuman CA, Beno MA, Christoph GG. Reappraisal of the stereochemistry of electrophilic additions to 3-norcarenes. X-ray and proton NMR analysis of norcarene epoxide conformation. The role of magnetic anisotropic contributions of epoxide rings Journal of the American Chemical Society. 101: 4645-4655. DOI: 10.1021/Ja00510A034 |
0.309 |
|
1979 |
Gardlik JM, Paquette LA. Bond fixation in annulenes. 7. Direct resolution of chiral cyclooctatetraenes Tetrahedron Letters. 20: 3597-3600. DOI: 10.1016/S0040-4039(01)95473-5 |
0.318 |
|
1979 |
Paquette LA. The development of polyquinane chemistry Cheminform. 10: 41-165. DOI: 10.1007/Bfb0048476 |
0.326 |
|
1979 |
Fristad WE, Han Y, Paquette LA. Silanes in organic synthesis: VI. Conversion of unsubstituted and 2-aryl ketones to (1-arylallyl)silanes Cheminform. 10: 27-40. DOI: 10.1002/Chin.197947270 |
0.397 |
|
1979 |
Paquette LA, Fristad WE, Schuman CA, Beno MA, Christoph GG. Reappraisal Of The Stereochemistry Of Electrophilic Additions To 3-Norcarenes. X-Ray And Proton Nmr Analysis Of Norcarene Epoxide Conformation. The Role O Magnetic Anisotropic Contributions Of Epoxide Rings Cheminform. 10. DOI: 10.1002/Chin.197947093 |
0.303 |
|
1979 |
Paquette LA, Browne AR, Chamot E. Productive Synthesis Of Heptalene From Naphthalene Via A Bis(Bicyclo(1.1.0)Butane) Derivative Cheminform. 10. DOI: 10.1002/Chin.197943194 |
0.373 |
|
1979 |
Wells G, Hanzawa Y, Paquette LA. 1,3-Di-Tert-Butylcyclooctatetraene Cheminform. 10. DOI: 10.1002/Chin.197943193 |
0.323 |
|
1979 |
Fristad WE, Dime DS, Bailey TR, Paquette LA. Silanes In Organic Synthesis. Part 5. Vinylsilane Mediated Regiospecific Cyclopentenone Annulation Of Ketones Cheminform. 10. DOI: 10.1002/Chin.197937176 |
0.344 |
|
1979 |
Paquette LA, Browne AR, Chamot E. An Expeditious Synthesis of Heptalene from Naphthalene via a Bis(bicyclo[1.1.0]butane) Intermediate Angewandte Chemie. 18: 546-547. DOI: 10.1002/Anie.197905461 |
0.427 |
|
1979 |
Paquette LA, Browne AR, Chamot E. Ergiebige Synthese von Heptalen aus Naphthalin über ein Bis(bicyclo[1.1.0]butan)‐Derivat Angewandte Chemie. 91: 581-582. DOI: 10.1002/Ange.19790910724 |
0.306 |
|
1979 |
Wells G, Hanzawa Y, Paquette LA. 1, 3-Di-tert-butylcyclooctatetraen Angewandte Chemie. 91: 578-579. DOI: 10.1002/Ange.19790910722 |
0.311 |
|
1978 |
Paquette LA, Ewing GD, Ley SV, Berk HC, Traynor SG. Synthesis and reducibility of homo-2-methoxyazocines and their benzo-fused derivatives. An examination of heteroatomic influences on the possible generation of 9C-10.pi. homoaromatic dianions The Journal of Organic Chemistry. 43: 4712-4720. DOI: 10.1021/Jo00419A007 |
0.487 |
|
1978 |
Chamot E, Paquette LA. Silver(I) ion catalyzed rearrangements of strained .sigma. bonds. 37. Steric inhibition of a silver(I)-catalyzed 1,8-bishomocubana-snoutane rearrangement Journal of Organic Chemistry. 43: 4527-4530. DOI: 10.1021/Jo00417A031 |
0.303 |
|
1978 |
Fristad WE, Bailey TR, Paquette LA. 1,2-Transposition of ketones via vinylsilanes Journal of Organic Chemistry. 43: 1620-1623. DOI: 10.1021/Jo00402A043 |
0.372 |
|
1978 |
Detty MR, Paquette LA. Comparative study of syn- and anti-1,5-bishomocycloheptatrien-2-yl radicals and carbocations Journal of Organic Chemistry. 43: 1118-1121. DOI: 10.1021/Jo00400A021 |
0.509 |
|
1978 |
Taylor RT, Paquette LA. Silver (I) ion catalyzed rearrangements of strained .delta. bonds. 34. A study of the capacity of Group 4 substituents for directing the course of silver(I)-catalyzed tricyclo[4.1.0.02,7]heptane rearrangement into the elusive type .delta. manifold Journal of Organic Chemistry. 43: 242-250. DOI: 10.1021/Jo00396A014 |
0.336 |
|
1978 |
Paquette LA, Detty MR. Synthesis and protonation studies of syn- and anti-2,4-bishomotropone. Comparison with the behavior of epimeric 2,4-bishomocycloheptatrienols under long- and short-lived ionization conditions Journal of the American Chemical Society. 100: 5856-5863. DOI: 10.1021/Ja00486A043 |
0.52 |
|
1978 |
Paquette LA, Wyvratt MJ, Berk HC, Moerck RE. Domino Diels-Alder reactions. 6. Domino Diels-Alder cycloadditions to 9,10-dihydrofulvalene and 11,12-dihydrosesquifulvalene. A synthetic tool for the elaboration of polycondensed alicyclic systems Journal of the American Chemical Society. 100: 5845-5855. DOI: 10.1021/Ja00486A042 |
0.33 |
|
1978 |
Spanget-Larsen J, Gleiter R, Detty MR, Paquette LA. Interaction of Walsh orbitals in trishomocycloheptatrienes and related hydrocarbons Journal of the American Chemical Society. 100: 3005-3014. DOI: 10.1021/Ja00478A012 |
0.414 |
|
1978 |
Paquette LA, Snow RA, Muthard JL, Cynkowski T. Domino Diels-Alder reactions. 4. C16-Hexaquinacene Journal of the American Chemical Society. 100: 1600-1602. DOI: 10.1021/Ja00473A046 |
0.334 |
|
1978 |
Paquette LA, Moerck RE, Harirchian B, Magnus PD. Use of phenyl vinyl sulfoxide as an acetylene equivalent in Diels-Alder cycloadditions Journal of the American Chemical Society. 100: 1597-1599. DOI: 10.1021/Ja00473A044 |
0.343 |
|
1978 |
Paquette LA, Detty MR. The rhodium (I)-catalyzed rearraugememt of syn-1,3-bishomocycloheptatriene Tetrahedron Letters. 19: 713-716. DOI: 10.1016/S0040-4039(01)85374-0 |
0.596 |
|
1978 |
Paquette LA, Grée R. Rhodium(I) catalysis of cycloprop[a]acenaphthylene isomerizations Journal of Organometallic Chemistry. 146: 319-329. DOI: 10.1016/S0022-328X(00)88759-8 |
0.35 |
|
1978 |
Paquette LA, Bunson RL. Substituent influences on the cope equilibrium in semibullvalene Tetrahedron. 34: 1301-1306. DOI: 10.1016/0040-4020(78)88323-9 |
0.343 |
|
1978 |
SPANGET-LARSEN J, GLEITER R, DETTY MR, PAQUETTE LA. ChemInform Abstract: INTERACTION OF WALSH ORBITALS IN TRISHOMOCYCLOHEPTATRIENES AND RELATED HYDROCARBONS Chemischer Informationsdienst. 9. DOI: 10.1002/Chin.197834048 |
0.435 |
|
1977 |
Paquette LA, Wallis TG, Kempe T, Christoph GG, Springer JP, Clardy J. Silver(I) ion catalyzed rearrangements of strained .sigma. bonds. 33. Benzoannulation as a probe of structural dimension and .pi.-electron distribution in elassovalenes. A mathematical model for the assessment of homoaromaticity Journal of the American Chemical Society. 99: 6946-6954. DOI: 10.1021/Ja00463A029 |
0.332 |
|
1977 |
Paquette L, Carmody M. Additions and Corrections - Thermally Promoted Ring Cleavage Reactions of Stereoisomeric Tetracyclo[4.3.0.02,5.07,9]non-3-enes. Pentacycl[5.3.0.02,6.03,5.08,10]decanes and Their Epoxide Counterparts Journal of the American Chemical Society. 99: 6153-6153. DOI: 10.1021/Ja00460A601 |
0.365 |
|
1977 |
Paquette LA, Taylor RT. The consequences of methyl substitution on the efficiency and regioselectivity of C-H insertion during intramolecular cyclization of norcaran-7-, 3-norcaren-7-, and tricyclo[5.1.0.03,5]octan-8-ylidenes Journal of the American Chemical Society. 99: 5708-5715. DOI: 10.1021/Ja00459A031 |
0.358 |
|
1977 |
Paquette LA, Kukla MJ, Ley SV, Traynor SG. The question of delocalization in "anchored" ions with potential trishomoaromatic character. 1. Reduction of tricyclo[5.4.1.04,12]dodeca-2,5,8,10-tetraene as a route to the 10.pi.11C dianion Journal of the American Chemical Society. 99: 4756-4763. DOI: 10.1021/Ja00456A037 |
0.416 |
|
1977 |
Paquette LA, Wallis TG, Hirotsu K, Clardy J. Stereospecific [3,3] shift of a cyclobutene ring involving photofragmentation of a 1,8-bishomocubane as the relay Journal of the American Chemical Society. 99: 2815-2816. DOI: 10.1021/Ja00450A077 |
0.375 |
|
1977 |
Detty MR, Paquette LA. The fate of bishomocycloheptadienyl cations generated by deamination Journal of the American Chemical Society. 99: 834-842. DOI: 10.1021/Ja00445A028 |
0.511 |
|
1977 |
Paquette LA, Detty MR. Stereoisomeric bishomo-3,5-cycloheptadienyl p-toluenesulfonates as probes of the geometric and conformational dependence to long-range cyclopropyl interaction during acetolysis Journal of the American Chemical Society. 99: 828-834. DOI: 10.1021/Ja00445A027 |
0.49 |
|
1977 |
Detty MR, Paquette LA. The question of hexahomobenzene automerization. New synthetic approaches to cis3-1,4,7-cyclononatriene Tetrahedron Letters. 18: 347-350. DOI: 10.1016/S0040-4039(01)92633-4 |
0.503 |
|
1977 |
Taylor RT, Degenhardt CR, Melega WP, Paquette LA. Direct conversion of ketones to vinylsilanes, -germanes, and -stannanes Tetrahedron Letters. 18: 159-162. DOI: 10.1016/S0040-4039(01)92576-6 |
0.345 |
|
1977 |
Detty MR, Paquette LA. The Fate Of Bishomocycloheptadienyl Cations Generated By Deamination Cheminform. 8. DOI: 10.1002/Chin.197717133 |
0.511 |
|
1977 |
PAQUETTE LA, DETTY MR. ChemInform Abstract: STEREOISOMERIC BISHOMO-3,5-CYCLOHEPTADIENYL P-TOLUENESULFONATES AS PROBES OF THE GEOMETRIC AND CONFORMATIONAL DEPENDENCE TO LONG-RANGE CYCLOPROPYL INTERACTION DURING ACETOLYSIS Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/chin.197717093 |
0.442 |
|
1977 |
PAQUETTE LA, LEY SV, TRAYNOR SG, MARTIN JT, GECKLE JM. ChemInform Abstract: FORMATION OF MONOHOMOCYCLOOCTATETRAENE DIANIONS IN LIQUID AMMONIA. ANALYSIS OF THE NUCLEOPHILIC REACTIVITY OF THE CYCLONONATRIENYL ANIONS GENERATED UPO SOLVENT PROTONATION Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/Chin.197710132 |
0.429 |
|
1976 |
Paquette LA, Klobucar WD, Snow RA. Halothiation as a Method for Oxidation of Primary Halides and Terminal Olefins to Aldehydes Synthetic Communications. 6: 575-581. DOI: 10.1080/00397917608063551 |
0.394 |
|
1976 |
Paquette LA, Itoh I, Lipkowitz KB. Synthesis and reactivity patterns of meso- and dl-bistriquinacene. Efficient route to the diastereomeric bivalvanes Journal of Organic Chemistry. 41: 3524-3529. DOI: 10.1021/Jo00884A007 |
0.336 |
|
1976 |
Paquette LA, Carmody MJ. Thermally promoted ring cleavage reactions of stereoisomeric tetracyclo[4.3.0.02,5.07,9]non-3-enes, pentacyclo[5.3.0.02,6.03,5.08,10]decanes, and their epoxide counterparts Journal of the American Chemical Society. 98: 8175-8181. DOI: 10.1021/Ja00441A048 |
0.36 |
|
1976 |
Paquette LA, Ley SV, Traynor SG, Martin JT, Geckle JM. Formation of monohomocyclooctatetraene dianions in liquid ammonia. Analysis of the nucleophilic reactivity of the cyclononatrienyl anions generated upon solvent protonation Journal of the American Chemical Society. 98: 8162-8172. DOI: 10.1021/Ja00441A046 |
0.419 |
|
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