Year |
Citation |
Score |
2015 |
Bobinski TP, Fuchs PL. Citric acid mediated catalytic osmylation/oxidative cleavage of electron deficient olefins: A vinyl sulfone study Tetrahedron Letters. 56: 4151-4154. DOI: 10.1016/J.Tetlet.2015.05.044 |
0.792 |
|
2015 |
Bobinski TP, Fuchs PL. Mechanism-specified 5-exo termini differentiation of a C32-desmethyl C28-C34 aplyronine A analog segment Tetrahedron Letters. 56: 3868-3871. DOI: 10.1016/J.Tetlet.2015.04.098 |
0.791 |
|
2013 |
Kanduluru AK, Banerjee P, Beutler JA, Fuchs PL. A convergent total synthesis of the potent cephalostatin/ritterazine hybrid -25-epi ritterostatin GN1N. The Journal of Organic Chemistry. 78: 9085-92. PMID 23899273 DOI: 10.1021/Jo401171Q |
0.459 |
|
2012 |
Sikervar V, Fleet JC, Fuchs PL. A general approach to the synthesis of enantiopure 19-nor-vitamin D3 and its C-2 phosphate analogs prepared from cyclohexadienyl sulfone. Chemical Communications (Cambridge, England). 48: 9077-9. PMID 22852135 DOI: 10.1039/C2Cc33054G |
0.421 |
|
2012 |
Sikervar V, Fuchs PL. Intramolecular methylation of an allyl sulfone via lithium alkoxyaluminate; application to the enantioselective synthesis of the CD ring of vitamin D3. Organic Letters. 14: 2922-4. PMID 22591038 DOI: 10.1021/Ol301144A |
0.344 |
|
2012 |
Ebrahimian GR, du Jourdin XM, Fuchs PL. Jacobsen protocols for large-scale epoxidation of cyclic dienyl sulfones: application to the (+)-pretazettine core. Organic Letters. 14: 2630-3. PMID 22545718 DOI: 10.1021/Ol300996M |
0.775 |
|
2012 |
Sikervar V, Fleet JC, Fuchs PL. Fluoride-mediated elimination of allyl sulfones: application to the synthesis of a 2,4-dimethyl-A-ring vitamin D3 analogue. The Journal of Organic Chemistry. 77: 5132-8. PMID 22533543 DOI: 10.1021/Jo300672A |
0.387 |
|
2011 |
Hong WP, Noshi MN, El-Awa A, Fuchs PL. Synthesis of the C1-C20 and C15-C27 segments of aplyronine A. Organic Letters. 13: 6342-5. PMID 22107608 DOI: 10.1021/Ol2024746 |
0.766 |
|
2011 |
Srinivasarao M, Kim Y, Li XH, Robbins DW, Fuchs PL. Studies on the synthesis of apoptolidin: synthesis of a C1-C27 fragment of apoptolidin D. The Journal of Organic Chemistry. 76: 7834-41. PMID 21827193 DOI: 10.1021/Jo200934W |
0.809 |
|
2011 |
Srinivasarao M, Park T, Chen Y, Fuchs PL. Noteworthy observations accompanying synthesis of the apoptolidin disaccharide. Chemical Communications (Cambridge, England). 47: 5858-60. PMID 21503348 DOI: 10.1039/C1Cc11448D |
0.804 |
|
2011 |
Sikervar V, Fuchs PL. S(N)2' addition/1,2-elimination of dimethylsulfonium methylide with epoxy vinyl sulfones: synthesis of exocyclic cross-conjugated dienyl sulfones. Chemical Communications (Cambridge, England). 47: 3472-4. PMID 21305095 DOI: 10.1039/C0Cc05405D |
0.374 |
|
2011 |
Srinivasarao M, Kim Y, Li XH, Robbins DW, Fuchs PL. Correction to Studies on the Synthesis of Apoptolidin: Synthesis of a C1–C27Fragment of Apoptolidin D The Journal of Organic Chemistry. 76: 9861-9861. DOI: 10.1021/Jo202181J |
0.764 |
|
2010 |
LaCour TG, Fuchs PL. ChemInform Abstract: Cephalostatin Synthesis. Part 17. Concurrent Ring Opening and Halogenation of Spiroketals. Cheminform. 30: no-no. DOI: 10.1002/chin.199934213 |
0.74 |
|
2010 |
Kim S, Sutton SC, Guo C, LaCour TG, Fuchs PL. ChemInform Abstract: Cephalostatin Synthesis. Part 13. Synthesis of the North 1 Unit of the Cephalostatin Family from Hecogenin Acetate. Cheminform. 30: no-no. DOI: 10.1002/chin.199925226 |
0.725 |
|
2010 |
LACOUR TG, GUO C, BHANDARU S, BOYD MR, FUCHS PL. ChemInform Abstract: Cephalostatin Synthesis. Part 11. Interphylal Product Splicing: The First Total Syntheses of Cephalostatin 1, the North Hemisphere of Ritterazine G, and the Highly Active Hybrid Analogue, Ritterostatin GN1N. Cheminform. 29: no-no. DOI: 10.1002/chin.199825284 |
0.705 |
|
2010 |
HENTEMANN MF, FUCHS PL. ChemInform Abstract: Synthesis via Vinyl Sulfones. Part 74. Scope and Limitations in the Jacobsen Epoxidation of Dienyl Sulfones. Cheminform. 28: no-no. DOI: 10.1002/chin.199745038 |
0.376 |
|
2010 |
XIANG J, FUCHS PL. ChemInform Abstract: Triflone Chemistry. Part 7. Syntheses via Vinyl Sulfones. Part 68. Alkenylation of C-H Bonds via Reaction with Vinyl and Dienyl Triflones. Stereospecific Synthesis of Trisubstituted Vinyl Triflones via Organocopper Addition to Acetyle Cheminform. 28: no-no. DOI: 10.1002/chin.199712068 |
0.343 |
|
2010 |
GUO C, BHANDARU S, FUCHS PL, BOYD MR. ChemInform Abstract: Cephalostatin Synthesis. Part 10. An Efficient Protocol for the Synthesis of Unsymmetrical Pyrazines. Total Synthesis of Dihydrocephalostatin 1 Cheminform. 28: no-no. DOI: 10.1002/chin.199708195 |
0.339 |
|
2010 |
JIN Z, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 66. Palladium(0)-Mediated Aminospirocyclization of Tertiary Allylic Sulfones. Stereospecific Construction of the Azabicyclic Ring System of Cephalotaxine. Cheminform. 27: no-no. DOI: 10.1002/chin.199646139 |
0.32 |
|
2010 |
KIM SH, FUCHS PL. ChemInform Abstract: Synthesis via Vinyl Sulfones. Part 63. Conversion of δ-(Sulfonyl) amino-α-epoxy Ketones to Bicyclic Ketopyrroles via Intramolecular Conjugate-Addition to Azoene Intermediates. Synthesis of the Bicyclic Ketopyrrole Core of the 1-Azaful Cheminform. 27: no-no. DOI: 10.1002/chin.199629144 |
0.366 |
|
2010 |
BHANDARU S, FUCHS PL. ChemInform Abstract: Cephalostatin Chemistry. Part 8. Synthesis of a C14′,15′ Dihydro Derivative of the South Hexacyclic Steroid Unit of Cephalostatin 1. Part 2. Spiroketal Synthesis and Stereochemical Assignment by NMR Spectroscopy. Cheminform. 27: no-no. DOI: 10.1002/chin.199610255 |
0.329 |
|
2010 |
KIM SH, JIN Z, MA S, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 60. Conversion of Vinyl Sulfones to Regiospecifically Functionalized Trisubstituted Olefins. Cheminform. 26: no-no. DOI: 10.1002/chin.199545049 |
0.301 |
|
2010 |
SMITH DC, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 58. A Triply Convergent Total Synthesis of a Symchiral Pyrrolidine-Fused Prostacyclin Analogue (IX). Cheminform. 26: no-no. DOI: 10.1002/chin.199537272 |
0.366 |
|
2010 |
JIN Z, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 56. Addition of γ-Methoxy Allylsulfonyl Anions to Cyclopentenyl Phenyl Sulfones. A Facile Synthesis of β-Cyclopentenyl-Substituted Dienones and Trienones. Cheminform. 26: no-no. DOI: 10.1002/chin.199531040 |
0.31 |
|
2010 |
KIM S, FUCHS PL. ChemInform Abstract: Cephalostatin Chemistry. Part 4. Application of the Reich Iodoso syn- Elimination for the Preparation of an Intermediate Appropriate for the Synthesis of Both Hexacyclic Steroidal Units of Cephalostatin 7. Cheminform. 26: no-no. DOI: 10.1002/chin.199515302 |
0.328 |
|
2010 |
MAHADEVAN A, FUCHS PL. ChemInform Abstract: Synthesis via Vinyl Sulfones. Part 53. A Mild and Convenient Synthesis of Functionalized Methyl Triflones and Vinyl Triflones. Cheminform. 26: no-no. DOI: 10.1002/chin.199501105 |
0.341 |
|
2010 |
JIN Z, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 52. A Highly Efficient Synthesis of β-Substituted Six- and Seven-Membered-Ring Enones via Carbon Alkylation of γ-Methoxy Allylsulfonyl Anions. Cheminform. 25: no-no. DOI: 10.1002/chin.199449114 |
0.321 |
|
2010 |
LEE SW, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 48. Comparison of Vinyl Organolithium and Organopalladium Reagents for Intramolecular Conjugate Addition to Vinyl Sulfones. Cheminform. 24: no-no. DOI: 10.1002/chin.199352162 |
0.357 |
|
2010 |
JIN Z, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 47. Regiospecific Silver(I)- Promoted, Palladium(0)-Catalyzed Intramolecular Addition of Aryl Iodides to Vinyl Sulfones. Cheminform. 24: no-no. DOI: 10.1002/chin.199352097 |
0.36 |
|
2010 |
LI C, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 46. Intramolecular Photocyclization of Aryl Vinyl Sulfones. Cheminform. 24: no-no. DOI: 10.1002/chin.199333094 |
0.361 |
|
2010 |
NEVILL CRJ, BRAISH TF, JAKUBOWSKI JA, FUCHS PL. ChemInform Abstract: Synthesis via Vinyl Sulfones. Part 31. Total Synthesis of a Homochiral Arene-Fused Prostacyclin Analog. Cheminform. 23: no-no. DOI: 10.1002/chin.199239164 |
0.375 |
|
2010 |
NEVILL CRJ, JAKUBOWSKI JA, FUCHS PL. ChemInform Abstract: Synthesis via Vinyl Sulfones. Part 33. Triply-Convergent Synthesis of Two Sets of Homochiral Cyclopent(a)indene Carbacyclin Analogs. Cheminform. 23: no-no. DOI: 10.1002/chin.199239163 |
0.331 |
|
2010 |
HARDINGER SA, JAKUBOWSKI JA, FUCHS PL. ChemInform Abstract: Synthesis via Vinyl Sulfones. Part 30. Triply-Convergent Total Synthesis of a Homochiral Benzoindane-Fused Prostacyclin Analog. Cheminform. 23: no-no. DOI: 10.1002/chin.199239162 |
0.771 |
|
2010 |
MAGAR SS, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 44. Bisalkylation of Dimetalated Phenylsulfonylmethyl Triflone. A (n + 1)Annulation Strategy for Synthesis of Cyclic Vinyl Sulfones. Cheminform. 23: no-no. DOI: 10.1002/chin.199237147 |
0.306 |
|
2010 |
LEE SW, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 43. Controlled Endocyclic and Exocyclic γ-Metalations of β-Substituted Cyclohexenyl Sulfones. Regiospecific Syntheses of γ-Oxygenated Cyclohexenyl Sulfones. Cheminform. 23: no-no. DOI: 10.1002/chin.199213174 |
0.615 |
|
2010 |
BURKHOLDER TP, FUCHS PL. ChemInform Abstract: Synthesis via Vinyl Sulfones. Part 38. Total Synthesis of the Cephalotaxus Alkaloids dl-Cephalotaxine, dl-11-Hydroxycephalotaxine, and dl-Drupacine. Cheminform. 22: no-no. DOI: 10.1002/chin.199114273 |
0.327 |
|
2009 |
Hong WP, El-Awa A, Fuchs PL. Reagent-directed allylic quadraselection. Chemoselective anti- and syn-Lawton S(N)2' methylation of seven-membered epoxyvinylsulfones. Journal of the American Chemical Society. 131: 9150-1. PMID 19534468 DOI: 10.1021/Ja9017557 |
0.776 |
|
2009 |
Lee S, LaCour TG, Fuchs PL. Chemistry of trisdecacyclic pyrazine antineoplastics: the cephalostatins and ritterazines. Chemical Reviews. 109: 2275-314. PMID 19438206 DOI: 10.1021/Cr800365M |
0.785 |
|
2009 |
El-Awa A, Noshi MN, du Jourdin XM, Fuchs PL. Evolving organic synthesis fostered by the pluripotent phenylsulfone moiety. Chemical Reviews. 109: 2315-49. PMID 19438205 DOI: 10.1021/Cr800309R |
0.776 |
|
2009 |
Mollat du Jourdin X, Noshi M, Fuchs PL. Designer discodermolide segments via ozonolysis of vinyl phosphonates. Organic Letters. 11: 543-6. PMID 19117490 DOI: 10.1021/Ol802503H |
0.78 |
|
2009 |
Lee S, Jamieson D, Fuchs PL. Synthesis of C14,15-dihydro-C22,25-epi north unit of cephalostatin 1 via "red-ox" modifications of hecogenin acetate. Organic Letters. 11: 5-8. PMID 19055428 DOI: 10.1021/Ol802122P |
0.804 |
|
2009 |
Mollat du Jourdin X, Noshi M, Fuchs PL. ChemInform Abstract: Synthesis via Vinyl Sulfones. Part 96. Chiral Carbon Collection. Part 18. Designer Discodermolide Segments via Ozonolysis of Vinyl Phosphonates. Cheminform. 40. DOI: 10.1002/chin.200925202 |
0.794 |
|
2008 |
Noshi MN, El-Awa A, Fuchs PL. Second-generation synthesis of syn- and anti-cycloheptadienylsulfone polyketide stereodiads. The Journal of Organic Chemistry. 73: 3274-7. PMID 18348572 DOI: 10.1021/Jo702353E |
0.793 |
|
2007 |
Noshi MN, El-awa A, Torres E, Fuchs PL. Conversion of cyclic vinyl sulfones to transposed vinyl phosphonates. Journal of the American Chemical Society. 129: 11242-7. PMID 17696536 DOI: 10.1021/Ja072890P |
0.795 |
|
2007 |
Lee JS, Cao H, Fuchs PL. Ruthenium-catalyzed mild C-H oxyfunctionalization of cyclic steroidal ethers. The Journal of Organic Chemistry. 72: 5820-3. PMID 17590044 DOI: 10.1021/Jo070382S |
0.394 |
|
2007 |
El-Awa A, du Jourdin XM, Fuchs PL. Asymmetric synthesis of all eight seven-carbon dipropionate stereotetrads. Journal of the American Chemical Society. 129: 9086-93. PMID 17567130 DOI: 10.1021/Ja071217X |
0.817 |
|
2007 |
Kim Y, Fuchs PL. Lactol-directed osmylation. Stereodivergent synthesis of four C-19,20 apoptolidin diols from a single allylic hemiacetal. Organic Letters. 9: 2445-8. PMID 17539652 DOI: 10.1021/Ol0707564 |
0.705 |
|
2007 |
Stockman R, Fuchs P, Karatholuvhu M, Sinclair A, Newton A, Alcaraz M. Synthesis of dl-Histrionicotoxin Synfacts. 2007: 0243-0243. DOI: 10.1055/S-2007-968194 |
0.813 |
|
2006 |
Karatholuvhu MS, Sinclair A, Newton AF, Alcaraz ML, Stockman RA, Fuchs PL. A concise total synthesis of DL-histrionicotoxin. Journal of the American Chemical Society. 128: 12656-7. PMID 17002353 DOI: 10.1021/Ja065015X |
0.821 |
|
2006 |
El-Awa A, Fuchs P. Double Lawton SN2′ addition to epoxyvinyl sulfones: Selective construction of the stereotetrads of aplyronine A Organic Letters. 8: 2905-2908. PMID 16805513 DOI: 10.1021/Ol060530L |
0.786 |
|
2006 |
Lee S, Fuchs PL. In situ nitrosonium ion generation - α-Oximinylation of enol ethers from steroidal spiroketals: Introduction of C23 (R)-OH in cephalostatin intermediates Canadian Journal of Chemistry. 84: 1442-1447. DOI: 10.1139/V06-113 |
0.666 |
|
2005 |
Lee JS, Fuchs PL. A biomimetically inspired, efficient synthesis of the South 7 hemisphere of cephalostatin 7. Journal of the American Chemical Society. 127: 13122-3. PMID 16173721 DOI: 10.1021/Ja0531935 |
0.463 |
|
2004 |
Karatholuvhu MS, Fuchs PL. 3,3,3-trichloropropyl-1-triphenylphosphorane: a reagent for the synthesis of (Z)-1,3-enynes, (Z,Z)-1-chloro-1,3-dienes, and 1,3-diynes. Journal of the American Chemical Society. 126: 14314-5. PMID 15521725 DOI: 10.1021/Ja045112V |
0.806 |
|
2004 |
Lee S, Fuchs PL. An efficient C-H oxidation protocol for alpha-hydroxylation of cyclic steroidal ethers. Organic Letters. 6: 1437-40. PMID 15101761 DOI: 10.1021/Ol049712A |
0.687 |
|
2004 |
Tong Z, Ma S, Fuchs PL. Synthesis of enantiopure five-carbon, stereodiads applicable for the preparation of the mycolactones Journal of Sulfur Chemistry. 25: 1-6. DOI: 10.1080/17415990410001661276 |
0.612 |
|
2004 |
Park T, Torres E, Fuchs PL. Improved and environmentally friendly large-scale preparation of cyclohexadienyl-, cycloheptadienyl sulfone and enantiopure epoxy cycloheptyl sulfones Synthesis. 1895-1900. DOI: 10.1055/S-2004-822318 |
0.685 |
|
2004 |
Li X, Lantrip D, Fuchs PL. Synthesis via Vinyl Sulfones. Part 88. γ-Allyl Phosphinoyl Phenyl Sulfone (GAPPS): A Conjunctive Reagent for the Synthesis of EE, EZ, and ET 1,3-Dienes. Cheminform. 35. DOI: 10.1002/chin.200412063 |
0.347 |
|
2003 |
Li X, Lantrip D, Fuchs PL. Gamma-allyl phosphinoyl phenyl sulfone (GAPPS): a conjunctive reagent for the synthesis of EE, EZ, and ET 1,3-dienes. Journal of the American Chemical Society. 125: 14262-3. PMID 14624559 DOI: 10.1021/Ja0377596 |
0.645 |
|
2003 |
Li W, Fuchs PL. Polyphosphoric acid trimethylsilyl ester promoted intramolecular acylation of an olefin by a carboxylic acid: convenient construction of C-18-functionalized delta14-hecogenin acetate. Organic Letters. 5: 4061-4. PMID 14572249 DOI: 10.1021/Ol035425F |
0.413 |
|
2003 |
Lee JS, Fuchs PL. Efficient protocol for ring opening of spiroketals using trifluoroacetyl trifluoromethanesulfonate (TFAT). Organic Letters. 5: 3619-22. PMID 14507187 DOI: 10.1021/Ol035284H |
0.407 |
|
2003 |
Li W, Fuchs PL. A new protocol for in situ dioxirane reactions: stoichiometric in oxone and catalytic in fluorinated acetophenones. Organic Letters. 5: 2853-6. PMID 12889891 DOI: 10.1021/Ol0348957 |
0.425 |
|
2003 |
Li W, Fuchs PL. An efficient synthesis of the C-23 deoxy, 17 alpha-hydroxy South 1 hemisphere and its cephalostatin 1 analog. Organic Letters. 5: 2849-52. PMID 12889890 DOI: 10.1021/Ol034894E |
0.387 |
|
2003 |
Torres E, Chen Y, Kim IC, Fuchs PL. Functionality propagation by alkylative oxidation of cross-conjugated cycloheptadienyl sulfones. Angewandte Chemie (International Ed. in English). 42: 3124-31. PMID 12866097 DOI: 10.1002/Anie.200350955 |
0.758 |
|
2003 |
Lee JS, Fuchs PL. New oxidative tools for the functionalization of the cephalostatin north 1 hemisphere. Organic Letters. 5: 2247-50. PMID 12816420 DOI: 10.1021/Ol034551G |
0.396 |
|
2003 |
Cacatian ST, Fuchs PL. Synthesis of allyl phosphine oxides/boranes via Horner reaction of bis(diphenylphosphine)ethane monoxide reagent with an aldehyde Tetrahedron. 59: 7177-7187. DOI: 10.1016/S0040-4020(03)01057-3 |
0.824 |
|
2002 |
Lee S, Fuchs PL. Chemospecific chromium[VI] catalyzed oxidation of C-H bonds at -40 degrees C1. Journal of the American Chemical Society. 124: 13978-9. PMID 12440880 DOI: 10.1021/Ja026734O |
0.656 |
|
2002 |
Chen Y, Evarts JB, Torres E, Fuchs PL. Synthesis of termini-differentiated 6-carbon stereotetrads: an alkylative oxidation strategy for preparation of the c21-c26 segment of apoptolidin(1). Organic Letters. 4: 3571-4. PMID 12375890 DOI: 10.1021/Ol026377M |
0.82 |
|
2002 |
Evarts J, Torres E, Fuchs PL. Syntheses of highly substituted enantiopure C6 and C7 enones(1). Journal of the American Chemical Society. 124: 11093-101. PMID 12224957 DOI: 10.1021/Ja026760M |
0.801 |
|
2002 |
Li W, LaCour TG, Fuchs PL. Dyotropic rearrangement facilitated proximal functionalization and oxidative removal of angular methyl groups: efficient syntheses of 23'-deoxy cephalostatin 1 analogues. Journal of the American Chemical Society. 124: 4548-9. PMID 11971687 DOI: 10.1021/Ja017323V |
0.766 |
|
2002 |
Lee S, Fuchs PL. The first total synthesis of (corrected) ritterazine M. Organic Letters. 4: 317-8. PMID 11820868 DOI: 10.1021/Ol016572L |
0.651 |
|
2002 |
Lee S, LaCour TG, Lantrip D, Fuchs PL. Redox refunctionalization of steroid spiroketals. Structure correction of ritterazine M. Organic Letters. 4: 313-6. PMID 11820867 DOI: 10.1021/Ol0165894 |
0.8 |
|
2002 |
Meyers DJ, Fuchs PL. Economical and environmentally friendly syntheses of 2-(phenylsulfonyl)-1,3-cyclohexadiene and 2-(phenylsulfonyl)-1,3-cycloheptadiene. The Journal of Organic Chemistry. 67: 200-4. PMID 11777460 DOI: 10.1021/Jo0107047 |
0.623 |
|
2001 |
Kim HY, Lantrip DA, Fuchs PL. Relative reactivity of anti- and syn-oximino carbonates and carbamates of 2-pyridylacetic acid esters. Organic Letters. 3: 2137-40. PMID 11440563 DOI: 10.1021/Ol015737N |
0.366 |
|
2001 |
Evarts JB, Fuchs PL. An efficient and convenient synthesis of enantiopure 4-(t-butyldimethylsilyloxy)-cyclohex-2-en-1-one: A formal synthesis of (±)-mesembranol Tetrahedron Letters. 42: 3673-3675. DOI: 10.1016/S0040-4039(01)00481-6 |
0.8 |
|
2000 |
Jiang W, Lantrip DA, Fuchs PL. Synthesis of enantiopure termini-differentiated heptane stereotriads. Application to side chain-functionalized tetrahydrofurans of IKD-8344. Organic Letters. 2: 2181-4. PMID 10930238 DOI: 10.1021/Ol005791O |
0.544 |
|
2000 |
LaCour TG, Guo C, Boyd MR, Fuchs PL. Outer-ring stereochemical modulation of cytotoxicity in cephalostatins. Organic Letters. 2: 33-6. PMID 10814239 DOI: 10.1021/Ol991153Y |
0.711 |
|
2000 |
Tong Z, Chen Y, Hentemann MF, Fuchs PL. Synthesis and oxidation reactions of cycloheptatrienyl sulfones Tetrahedron Letters. 41: 7795-7799. DOI: 10.1016/S0040-4039(00)01386-1 |
0.767 |
|
1999 |
LaCour TG, Tong Z, Fuchs PL. Consequences of acid catalysis in concurrent ring opening and halogenation of spiroketals. Organic Letters. 1: 1815-8. PMID 10836039 DOI: 10.1021/Ol991078R |
0.789 |
|
1999 |
Hentemann M, Fuchs PL. Asymmetric epoxy cyclohexenyl sulfones: readily accessible progenitors of stereo defined six-carbon arrays. Organic Letters. 1: 355-7. PMID 10822575 DOI: 10.1021/Ol990523F |
0.405 |
|
1999 |
Lee JW, Fuchs PL. Reduction of azides to primary amines in substrates bearing labile ester functionality. Synthesis of a PEG-solubilized, "Y"-shaped iminodiacetic acid reagent for preparation of folate-tethered drugs. Organic Letters. 1: 179-81. PMID 10822557 DOI: 10.1021/Ol9905248 |
0.392 |
|
1999 |
LaCour TG, Guo C, Ma S, Jeong JU, Boyd MR, Matsunaga S, Fusetani N, Fuchs PL. On topography and functionality in the B-D rings of cephalostatin cytotoxins. Bioorganic & Medicinal Chemistry Letters. 9: 2587-92. PMID 10498214 DOI: 10.1016/S0960-894X(99)00430-8 |
0.707 |
|
1999 |
Guo C, LaCour TG, Fuchs PL. On the relationship of OSW-1 to the cephalostatins. Bioorganic & Medicinal Chemistry Letters. 9: 419-24. PMID 10091695 DOI: 10.1016/S0960-894X(98)00743-4 |
0.717 |
|
1999 |
Jeong JU, Guo C, Fuchs PL. Synthesis of the South unit of cephalostatin. 7. Total syntheses of (+)- cephalostatin 7, (+)-cephalostatin 12, and (+)-ritterazine K Journal of the American Chemical Society. 121: 2071-2084. DOI: 10.1021/Ja9817141 |
0.345 |
|
1999 |
Kim S, Sutton SC, Guo C, LaCour TG, Fuchs PL. Synthesis of the North 1 unit of the cephalostatin family from hecogenin acetate Journal of the American Chemical Society. 121: 2056-2070. DOI: 10.1021/Ja9817139 |
0.726 |
|
1999 |
LaCour TG, Fuchs PL. Concurrent ring opening and halogenation of spiroketals Tetrahedron Letters. 40: 4655-4658. DOI: 10.1016/S0040-4039(99)00827-8 |
0.733 |
|
1999 |
Evarts JB, Fuchs PL. Synthesis of a family of epoxyvinyltriflate stereotetrads from 4- hydroxycyclohex-2-en-1-one Tetrahedron Letters. 40: 2703-2706. DOI: 10.1016/S0040-4039(99)00344-5 |
0.809 |
|
1999 |
Hentemann M, Fuchs PL. Synthesis of 6-carbon termini-differentiated stereotriads via symchiral 2-trifloxy-1,3-cyclohexadiene monoepoxidel Tetrahedron Letters. 40: 2699-2702. DOI: 10.1016/S0040-4039(99)00343-3 |
0.403 |
|
1998 |
LaCour TG, Guo C, Bhandaru S, Boyd MR, Fuchs PL. Interphylal product splicing: The first total syntheses of cephalostatin 1, the North hemisphere of ritterazine G, and the highly active hybrid analogue, ritterostatin G(N)1(N)1 Journal of the American Chemical Society. 120: 692-707. DOI: 10.1021/Ja972160P |
0.716 |
|
1998 |
Xiang J, Fuchs PL. Chemospecific alkynylation of organic iodides Tetrahedron Letters. 39: 8597-8600. DOI: 10.1016/S0040-4039(98)01924-8 |
0.327 |
|
1998 |
Xiang J, Evarts J, Rivkin A, Curran DP, Fuchs PL. Use of allylic trifiones for allylation of C-H bonds Tetrahedron Letters. 39: 4163-4166. DOI: 10.1016/S0040-4039(98)00775-8 |
0.798 |
|
1998 |
Guo C, Fuchs PL. The first synthesis of the aglycone of the potent anti-tumor steroidal saponin OSW-1 Tetrahedron Letters. 39: 1099-1102. DOI: 10.1016/S0040-4039(97)10814-0 |
0.38 |
|
1997 |
Van Dort PC, Fuchs PL. Free Radical Self-Immolative 1,2-Elimination and Reductive Desulfonylation of Aryl Sulfones Promoted by Intramolecular Reactions with Ortho-Attached Carbon-Centered Radicals(1). The Journal of Organic Chemistry. 62: 7142-7147. PMID 11671818 DOI: 10.1021/Jo970445E |
0.352 |
|
1997 |
Van Dort PC, Fuchs PL. Sulfones as Radical Progenitors: An Unprecedented Example of Homolytic Sulfone Cleavage Facilitated by o-Stannyl Substitution of Aryl Sulfones(1). The Journal of Organic Chemistry. 62: 7137-7141. PMID 11671817 DOI: 10.1021/Jo970338K |
0.378 |
|
1997 |
Luo J, Smith MD, Lantrip DA, Wang S, Fuchs PL. Efficient syntheses of pyrofolic acid and pteroyl azide, reagents for the production of carboxyl-differentiated derivatives of folic acid Journal of the American Chemical Society. 119: 10004-10013. DOI: 10.1021/Ja971568J |
0.387 |
|
1997 |
Xiang J, Jiang W, Gong J, Fuchs PL. Stereospecific alkenylation of C-H bonds via reaction with β- heteroatom-functionalized trisubstituted vinyl triflones Journal of the American Chemical Society. 119: 4123-4129. DOI: 10.1021/Ja963636S |
0.527 |
|
1997 |
Xiang J, Jiang W, Fuchs PL. Scope and limitations of functionalized acetylenic triflones in the direct alkynylation of C-H bonds Tetrahedron Letters. 38: 6635-6638. DOI: 10.1016/S0040-4039(97)01577-3 |
0.562 |
|
1997 |
Hentemann MF, Fuchs PL. Scope and limitations in the Jacobsen epoxidation of dienyl sulfones Tetrahedron Letters. 38: 5615-5618. DOI: 10.1016/S0040-4039(97)01275-6 |
0.394 |
|
1997 |
Kim SH, Figueroa I, Fuchs PL. Application of the Grubbs ring-closing metathesis for the construction of a macrocyclic ansa-bridge. Synthesis of the tricyclic core of roseophilin Tetrahedron Letters. 38: 2601-2604. DOI: 10.1016/S0040-4039(97)00424-3 |
0.416 |
|
1997 |
Gong J, Fuchs PL. Alkynylation of aldehydic C-H bonds via reaction with acetylenic triflones. Tetrahedron Letters. 38: 787-790. DOI: 10.1016/S0040-4039(96)02413-6 |
0.401 |
|
1996 |
Xiang J, Fuchs PL. Alkenylation of C-H bonds via reaction with vinyl and dienyl triflones. Stereospecific synthesis of trisubstituted vinyl triflones via organocopper addition to acetylenic triflones Journal of the American Chemical Society. 118: 11986-11987. DOI: 10.1021/Ja962790B |
0.412 |
|
1996 |
Guo C, Bhandaru S, Fuchs PL, Boyd MR. An efficient protocol for the synthesis of unsymmetrical pyrazines. Total synthesis of dihydrocephalostatin 1 Journal of the American Chemical Society. 118: 10672-10673. DOI: 10.1021/Ja962646Q |
0.426 |
|
1996 |
Xiang JS, Mahadevan A, Fuchs PL. Stereo-and regiospecific syntheses of α- and β-substituted vinyl and dienyl triflones via the stille reaction Journal of the American Chemical Society. 118: 4284-4290. DOI: 10.1021/Ja954303I |
0.386 |
|
1996 |
Xiang JS, Fuchs PL. Mechanistic aspects of the C-H alkynylation reaction of acetylenic triflones. Determination of phenyl versus cyclohexyl migratory aptitude for a vinylidine carbene Tetrahedron Letters. 37: 5269-5272. DOI: 10.1016/0040-4039(96)01117-3 |
0.405 |
|
1996 |
Jin Z, Fuchs PL. Use of phosphazene base and phase-transfer conditions for regiospecific alkylative isomerization of vinyl sulfones capable of undergoing β-elimination reactions Tetrahedron Letters. 37: 5249-5252. DOI: 10.1016/0040-4039(96)01111-2 |
0.312 |
|
1996 |
Jin Z, Kim SH, Fuchs PL. Phosphazene base P2-Et mediated isomerization of vinyl sulfones to allyl sulfones Tetrahedron Letters. 37: 5247-5248. DOI: 10.1016/0040-4039(96)01110-0 |
0.301 |
|
1996 |
Kim SH, Fuchs PL. Conversion of δ-(sulfonyl)amino-α-epoxy ketones to bicyclic ketopyrroles via intramolecular conjugate-addition to azoene intermediates. Synthesis of the bicyclic ketopyrrole core of the 1-azafulvene roseophilin Tetrahedron Letters. 37: 2545-2548. DOI: 10.1016/0040-4039(96)00390-5 |
0.428 |
|
1995 |
Smith DC, Fuchs PL. Syntheses Via Vinyl Sulfones. 58. A Triply Convergent Total Synthesis of a Symchiral Pyrrolidine-Fused Prostacyclin Analog The Journal of Organic Chemistry. 60: 2692-2703. DOI: 10.1021/Jo00114A016 |
0.464 |
|
1995 |
Mahadevan A, Fuchs PL. Synthesis via Vinyl Sulfones. 57. Facile Synthesis of Allyl, .gamma.-Iodoallyl, and Cyclopropyl Triflones via Radical-Mediated Atom-Transfer Addition of Iodomethyl Triflone to Olefins and Acetylenes Journal of the American Chemical Society. 117: 3272-3273. DOI: 10.1021/Ja00116A032 |
0.393 |
|
1995 |
Jin Z, Fuchs PL. Addition of .gamma.-Methoxy Allylsulfonyl Anions to Cyclopentenyl Phenyl Sulfones. A Facile Synthesis of .beta.-Cyclopentenyl-Substituted Dienones and Trienones Journal of the American Chemical Society. 117: 3022-3028. DOI: 10.1021/Ja00116A007 |
0.359 |
|
1995 |
Bhandaru S, Fuchs PL. Synthesis of a C14',15' dihydro derivative of the south hexacyclic steroid unit of cephalostatin 1. Part II: Spiroketal synthesis and stereochemical assignment by nmr spectroscopy Tetrahedron Letters. 36: 8351-8354. DOI: 10.1016/0040-4039(95)01805-R |
0.418 |
|
1995 |
Bhandaru S, Fuchs PL. Synthesis of a C14',15' dihydro derivative of the south hexacyclic steroid unit of cephalostatin 1. Part I : regiospecific Rh[II]-mediated intermolecular oxygen alkylation of a primary neopentyl alcohol Tetrahedron Letters. 36: 8347-8350. DOI: 10.1016/0040-4039(95)01804-Q |
0.417 |
|
1995 |
Kim SH, Jin Z, Fuchs PL. Synthesis of beta-substituted cyclopentenones via carbon alkylation of metalated gamma-methoxycyclopentenyl phenylsulfonyl anion Tetrahedron Letters. 36: 4537-4538. DOI: 10.1016/0040-4039(95)00822-T |
0.347 |
|
1995 |
Kim SH, Jin Z, Ma S, Fuchs PL. Conversion of vinyl sulfones to regiospecifically functionalized trisubstituted olefins Tetrahedron Letters. 36: 4013-4014. DOI: 10.1016/0040-4039(95)00701-D |
0.382 |
|
1995 |
Jeong JU, Fuchs PL. Synthesis of the South hexacyclic sterold unit of cephalostatin 7 Tetrahedron Letters. 36: 2431-2434. DOI: 10.1016/0040-4039(95)00308-Y |
0.336 |
|
1995 |
Kim S, Sutton SC, Fuchs PL. Chromium [II]-mediated reductive cleavage of a tertiary halide bearing three β-alkoxy groups. Synthesis of the north hexacyclic steroid unit of the cephalostatin family Tetrahedron Letters. 36: 2427-2430. DOI: 10.1016/0040-4039(95)00307-X |
0.368 |
|
1995 |
Smith DC, Fuchs PL. A triply convergent total synthesis of a symchiral pyrrolidine-fused prostacyclin analog Journal of Organic Chemistry. 60: 2692-2703. |
0.319 |
|
1994 |
Jakubowski JA, Utterback BG, Mais DE, Hardinger SA, Braish TF, Nevill CR, Fuchs PL. Biochemical and pharmacological activity of arene-fused prostacyclin analogues on human platelets. Prostaglandins. 47: 189-201. PMID 8016389 DOI: 10.1016/0090-6980(94)90060-4 |
0.705 |
|
1994 |
Jin Z, Vandort PC, Fuchs PL. New Synthetic Methods Exploiting Vinyl Sulfones Discovered During the Synthesis of a Natural Product Phosphorus, Sulfur, and Silicon and the Related Elements. 95: 1-19. DOI: 10.1080/10426509408034198 |
0.437 |
|
1994 |
Mahadevan A, Li C, Fuchs PL. Silver fluoroborate promoted sulfur alkylation of β-silyl ethyl sulfides. Selective synthesis of β-thioglycosides Synthetic Communications. 24: 3099-3107. DOI: 10.1080/00397919408011323 |
0.304 |
|
1994 |
Smith DC, Lee SW, Fuchs PL. Conversion of amides and lactams to thioamides and thiolactams using hexamethyldisilathiane Journal of Organic Chemistry. 59: 348-354. DOI: 10.1021/Jo00081A011 |
0.393 |
|
1994 |
Jin Z, Fuchs PL. A Highly Efficient Synthesis of .beta.-Substituted Six- and Seven-Membered-Ring Enones via Carbon Alkylation of .gamma.-Methoxy Allylsulfonyl Anions Journal of the American Chemical Society. 116: 5995-5996. DOI: 10.1021/Ja00092A071 |
0.388 |
|
1994 |
Jeong JU, Fuchs PL. Synthesis of a 17-deoxy, C-14,15-dihydro derivative of the North Spiroketal moiety of the cephalostatins. Conversion to a (+)-trisdecacyclic C2 symmetrical pyrazine Journal of the American Chemical Society. 116: 773-774. DOI: 10.1021/Ja00081A050 |
0.401 |
|
1994 |
Li C, Fuchs PL. Methanesulfenyl triflate promoted iminosulfenylation of an allylic trichloroacetimidate. An efficient and stereospecific total synthesis of (+) mannostatin A Tetrahedron Letters. 35: 5121-5124. DOI: 10.1016/S0040-4039(00)77043-2 |
0.416 |
|
1994 |
Li C, Shih TL, Jeong JU, Arasappan A, Fuchs PL. The use of tetramethylguanidinium azide in non-halogenated solvents avoids potential explosion hazards Tetrahedron Letters. 35: 2645-2646. DOI: 10.1016/S0040-4039(00)76995-4 |
0.401 |
|
1994 |
Jeong JU, Fuchs PL. Spiroketal equilibration: Interconversion of 1,6-dioxaspiro[4.4]nonanes and 1,6-dioxaspiro[4.5]decanes. Implications for the synthesis of cephalostatin 7 Tetrahedron Letters. 35: 5385-5388. DOI: 10.1016/S0040-4039(00)73506-4 |
0.358 |
|
1994 |
Mahadevan A, Fuchs PL. A mild and convenient synthesis of functionalized methyl triflones and vinyl triflones Tetrahedron Letters. 35: 6025-6028. DOI: 10.1016/0040-4039(94)88065-4 |
0.479 |
|
1994 |
Kim S, Fuchs PL. Application of the Reich iodoso syn-elimination for the preparation of an intermediate appropriate for the synthesis of both hexacyclic steroidal units of cephalostatin 7 Tetrahedron Letters. 35: 7163-7166. DOI: 10.1016/0040-4039(94)85350-9 |
0.448 |
|
1993 |
Kim S, Fuchs PL. Oxidation and reduction reactions of highly functionalized allyl stannanes. Bicyclic and tricyclic .alpha.-stannylmethyl enones prepared via the Robinson annulation reaction of .beta.'-stannylethyl vinyl ketone Journal of the American Chemical Society. 115: 5934-5940. DOI: 10.1021/Ja00067A006 |
0.471 |
|
1993 |
Lamothe M, Fuchs PL. Intramolecular oxygen versus carbon alkylation of naphthoate esters. A caveat on the mechanistic aspects of neocarzinostatin chemistry Journal of the American Chemical Society. 115: 4483-4496. DOI: 10.1021/Ja00064A010 |
0.406 |
|
1993 |
Li C, Fuchs PL. Intramolecular photocyclization of aryl vinyl sulfones Tetrahedron Letters. 34: 1855-1858. DOI: 10.1016/S0040-4039(00)91946-4 |
0.401 |
|
1993 |
Who Lee S, Fuchs PL. Comparison of vinyl organolithium and organopalladium reagents for intramolecular conjugate addition to vinyl sulfones Tetrahedron Letters. 34: 5209-5212. DOI: 10.1016/S0040-4039(00)73954-2 |
0.471 |
|
1993 |
Jin Z, Fuchs PL. Regiospecific silver[I] promoted, palladium[O]-catalyzed intramolecular addition of aryl iodides to vinyl sulfones Tetrahedron Letters. 34: 5205-5208. DOI: 10.1016/S0040-4039(00)73953-0 |
0.367 |
|
1993 |
Li C, Arasappan A, Fuchs PL. Tetramethylguanidinium azide as a new reagent for the stereoselective synthesis of glycosyl azides Tetrahedron Letters. 34: 3535-3538. DOI: 10.1016/S0040-4039(00)73629-X |
0.453 |
|
1992 |
Magar SS, Desai RC, Fuchs PL. Synthesis of phorbol C-ring analogs: A biomimetic model study on the phorbol to 12-hydroxydaphnetoxin conversion Journal of Organic Chemistry. 57: 5360-5369. DOI: 10.1021/Jo00046A017 |
0.445 |
|
1992 |
Pan Y, Merriman RL, Tanzer LR, Fuchs PL. Synthesis and pharmacological evaluation of nonacyclic and trisdecacyclic pyrazines related to cephalostatin Bioorganic and Medicinal Chemistry Letters. 2: 967-972. DOI: 10.1016/S0960-894X(00)80599-5 |
0.322 |
|
1992 |
Magar SS, Fuchs PL. Bis-alkylation of dimetallated phenylsulfonylmethyl triflone. A n+1 annulation strategy for synthesis of cyclic vinyl sulfones Tetrahedron Letters. 33: 745-748. DOI: 10.1016/S0040-4039(00)77705-7 |
0.409 |
|
1991 |
Berglund RA, Braish TF, Jakubowski JA, Fuchs PL. Triply-convergent synthesis of a homochiral 3,3-dimethyl, 15-cyclohexyl prostacyclin analog Bioorganic and Medicinal Chemistry Letters. 1: 649-652. DOI: 10.1016/S0960-894X(01)81170-7 |
0.395 |
|
1991 |
Nevill CR, Jakubowski JA, Fuchs PL. Triply-convergent synthesis of two sets of homochiral cyclopent[a]indene carbacyclin analogs Bioorganic and Medicinal Chemistry Letters. 1: 83-86. DOI: 10.1016/S0960-894X(01)81098-2 |
0.375 |
|
1991 |
Hardinger SA, Jakubowski JA, Fuchs PL. Triply-convergent syntheses of two homochiral arene-fused prostacyclin analogs related to U68,215 Bioorganic and Medicinal Chemistry Letters. 1: 79-82. DOI: 10.1016/S0960-894X(01)81097-0 |
0.722 |
|
1991 |
Nevill CR, Braish TF, Jakubowski JA, Fuchs PL. Total synthesis of a homochiral arene-fused prostacyclin analog Bioorganic and Medicinal Chemistry Letters. 1: 77-78. DOI: 10.1016/S0960-894X(01)81096-9 |
0.434 |
|
1991 |
Hardinger SA, Jakubowski JA, Fuchs PL. Tripyl-convergent total synthesis of a homochiral benzoindane-fused prostacyclin analog Bioorganic and Medicinal Chemistry Letters. 1: 73-76. DOI: 10.1016/S0960-894X(01)81095-7 |
0.768 |
|
1991 |
Lee SW, Fuchs PL. Controlled endocyclic and exocyclic γ-metalations of β-substituted cyclohexenyl sulfones. Regiospecific syntheses of γ-oxygenated cyclohexenyl sulfones Tetrahedron Letters. 32: 2861-2864. DOI: 10.1016/0040-4039(91)80632-G |
0.667 |
|
1991 |
Magar SS, Fuchs PL. Synthesis of tertiary alcohols via the use of the allyldimethylsilyl moiety as a latent hydroxyl group in the Kumada-Fleming-Tamao reaction Tetrahedron Letters. 32: 7513-7516. DOI: 10.1016/0040-4039(91)80521-7 |
0.395 |
|
1990 |
Nevill CR, Fuchs PL. Annulation reactions of ortho-chloromethyi. aryl cuprates1 Synthetic Communications. 20: 761-772. DOI: 10.1080/00397919008052320 |
0.363 |
|
1990 |
Scarpetti D, Fuchs PL. Fluoride ion mediated intramolecular sulfenylation of .alpha.-silyl sulfones: Ramberg-Baecklund annulation to exocyclic fused olefins Journal of the American Chemical Society. 112: 8084-8090. DOI: 10.1021/Ja00178A036 |
0.421 |
|
1990 |
NEVILL CRJ, FUCHS PL. ChemInform Abstract: Synthesis via Vinyl Sulfones. Part 40. Annulation Reactions of ortho-Chloromethylarylcuprates. Cheminform. 21. DOI: 10.1002/chin.199036147 |
0.351 |
|
1989 |
Berglund RA, Fuchs PL. Synthesis of Fluorinated Dienylic Stannanes Via the Wadsworth-Emmons Reaction Synthetic Communications. 19: 1965-1980. DOI: 10.1080/00397918908052589 |
0.384 |
|
1989 |
Pan Y, Hardinger SA, Fuchs PL. Sn2' Addition Of Organometalllc Reagents To R I -Amino Cyclohexenyl Sulfone Derivative Synthetic Communications. 19: 403-416. DOI: 10.1080/00397918908050680 |
0.754 |
|
1989 |
Ranasinghe MG, Fuchs PL. Ramberg-Bäcklund syntheses and chemodirected annulations of exocyclic allylsilanes Journal of the American Chemical Society. 111: 779-782. DOI: 10.1021/Ja00184A082 |
0.437 |
|
1989 |
Pan Y, Hutchinson DK, Nantz HH, Fuchs PL. SN2' Additions of cuprates to sulfone and ester-polarized cyclopentenylic systems1 1 Syntheses via vinyl sulfones 34. For a review on this subject see Fuchs, P.L.: Braish, T.F. Chem. Rev.1986, 86, 903 Tetrahedron. 45: 467-478. DOI: 10.1016/0040-4020(89)80074-2 |
0.344 |
|
1989 |
PAN Y, HARDINGER SA, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 35. SN2′ Addition of Organometallic Reagents to β′-Amino Cyclohexenyl Sulfone Derivatives. Cheminform. 20. DOI: 10.1002/chin.198951066 |
0.754 |
|
1989 |
PAN Y, HUTCHINSON DK, NANTZ MH, FUCHS PL. ChemInform Abstract: SN2′ Additions of Cuprates to Sulfone and Ester-Polarized Cyclopentenylic Systems. Cheminform. 20. DOI: 10.1002/chin.198922127 |
0.502 |
|
1989 |
RANASINGHE MG, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 36. Ramberg-Baecklund Syntheses and Chemodirected Annulations of Exocyclic Allylsilanes. Cheminform. 20. DOI: 10.1002/chin.198918139 |
0.321 |
|
1988 |
Palmer JT, Fuchs PL. Synthesis and alkylation of vinylsulfinic acids via fluoride cleavage of e-trimethylsilylethyl vinyl sulfones Synthetic Communications. 18: 233-245. DOI: 10.1080/00397918808057829 |
0.454 |
|
1988 |
Ranasinghe MG, Fuchs PL. A facile synthesis of unsymmetrical thiolsulfonates via sulfonylation of mercaptans Synthetic Communications. 18: 227-230. DOI: 10.1080/00397918808057828 |
0.447 |
|
1988 |
Toth JE, Hamann PR, Fuchs PL. Studies culminating in the total synthesis of (dl)-morphine Journal of Organic Chemistry. 53: 4694-4708. DOI: 10.1021/Jo00255A008 |
0.313 |
|
1988 |
Braish TF, Saddler JC, Fuchs PL. Syntheses via vinyl sulfones. 28. Seven-ring annulation. A linch-pin approach to a tetracyclic precursor of the lathrane diterpenes The Journal of Organic Chemistry. 53: 3647-3658. DOI: 10.1021/Jo00251A001 |
0.378 |
|
1988 |
Govindan SV, Fuchs PL. Regiospecific quassinoidal A-ring synthesis via an olefin oxidation strategy Journal of Organic Chemistry. 53: 2593-2597. DOI: 10.1021/Jo00246A036 |
0.42 |
|
1988 |
Burkholder TP, Fuchs PL. Synthesis via vinyl sulfones. 27. Total synthesis of cephalotaxine. The first example of an intramolecular [4 + 2] cycloaddition where the dienophile has been delivered from the face opposite to the tethering moiety Journal of the American Chemical Society. 110: 2341-2342. DOI: 10.1021/ja00215a076 |
0.338 |
|
1988 |
GOVINDAN SV, FUCHS PL. ChemInform Abstract: Bruceantin Support Studies. Part 14. Regiospecific Quassinoidal A-Ring Synthesis via an Olefin Oxidation Strategy. Cheminform. 19. DOI: 10.1002/chin.198842179 |
0.314 |
|
1988 |
NANTZ MH, FUCHS PL. ChemInform Abstract: Efficient Generation and Use of 3-Carbalkoxycyclopentadienone as a Diels-Alder Dienophile. Part 13. Cheminform. 19. DOI: 10.1002/chin.198817156 |
0.527 |
|
1988 |
NANTZ MH, FUCHS PL. ChemInform Abstract: Cycloaromatization Reactions of Methyl 4-Carboxymethyl-5-methoxypenta- 2,4-dienoate. Cheminform. 19. DOI: 10.1002/chin.198804092 |
0.554 |
|
1988 |
Anderson MB, Ranasinghe MG, Palmer JT, Fuchs PL. Nucleophilic and electrophilic mercaptanylations via 2-(trimethylsilyl)ethanethiol-derived reagents Journal of Organic Chemistry. 53: 3125-3127. |
0.301 |
|
1987 |
Anderson MB, Fuchs PL. An efficient method for conversion of carboxylic acid derivatives to allylsi lanes Synthetic Communications. 17: 621-635. DOI: 10.1080/00397918708075736 |
0.389 |
|
1987 |
Nantz MH, Fuchs PL. Cycloaromatization reactions of methyl 4-carbomethoxy-5-methoxy-penta-2,4 -dienoate Synthetic Communications. 17: 761-771. DOI: 10.1080/00397918708063931 |
0.642 |
|
1987 |
Nantz MH, Radisson X, Fuchs PL. Efficient 4+1 syntheses of highly functionalized cyclopentenes Synthetic Communications. 17: 55-69. DOI: 10.1080/00397918708063903 |
0.624 |
|
1987 |
Radisson X, Kwiatkowski PL, Fuchs PL. A Self-Immolative Strategy for 1,2-Elimination of Homallyl Sulfones to 1,3-Dienes Synthetic Communications. 17: 39-53. DOI: 10.1080/00397918708063902 |
0.306 |
|
1987 |
Hardinger SA, Fuchs PL. Synthesis of vinyl sulfones. 23. Addition of organometallic reagents to cyclooctenyl phenyl sulfones The Journal of Organic Chemistry. 52: 2739-2749. DOI: 10.1021/Jo00389A019 |
0.8 |
|
1987 |
Hedstrand DM, Byrn SR, McKenzie AT, Fuchs PL. Bruceantin support studies. 10. Use of an axial .beta.-face thiomethyl control element in intramolecular conjugate additions. Synthesis of a tricyclic bruceantin precursor The Journal of Organic Chemistry. 52: 592-598. DOI: 10.1021/Jo00380A020 |
0.308 |
|
1987 |
Conrad PC, Kwiatkowski PL, Fuchs PL. Synthesis via vinyl sulfones. 18. Rapid access to a series of highly functionalized .alpha.,.beta.-unsaturated cyclopentenones. A caveat on aminospirocyclization The Journal of Organic Chemistry. 52: 586-591. DOI: 10.1021/Jo00380A019 |
0.318 |
|
1987 |
Nantz MH, Fuchs PL. Efficient generation and use of 3-carboalkoxycyclopentadienone as a Diels-Alder dienophile Journal of Organic Chemistry. 52: 5298-5299. DOI: 10.1021/Jo00232A051 |
0.578 |
|
1987 |
Hutchinson DK, Fuchs PL. Synthesis via vinyl sulfones. 22. A chemodirected, triply-convergent total synthesis of d-(+)-carbacyclin Journal of the American Chemical Society. 109: 4755-4756. DOI: 10.1021/Ja00249A068 |
0.397 |
|
1987 |
Kuo F, Fuchs PL. Bruceantin support studies. 12. Synthesis of a pentacyclic ABCDE bruceantin intermediate Journal of the American Chemical Society. 109: 1122-1128. DOI: 10.1021/ja00238a022 |
0.301 |
|
1987 |
PALMER JT, LEARN KS, FUCHS PL. ChemInform Abstract: Cytolasin Report Studies. Part 8. Synthesis and Facile One-Pot Aldol/ Elimination/Diels-Alder Reaction of β-Keto-Z-dienylamides as Cytochalasin C Intermediates. Cheminform. 18. DOI: 10.1002/chin.198710216 |
0.319 |
|
1987 |
HENSEL MJ, FUCHS PL. ChemInform Abstract: Cytolasin Report Studies. Part 6. A Highly Selective Synthesis of a Chiral γ-Amino Trisubstituted Z-Vinyl Ester. Cheminform. 18. DOI: 10.1002/chin.198710172 |
0.303 |
|
1987 |
Hardinger SA, Fuchs PL. Addition of organometallic reagents to cyclooctenyl phenyl sulfones Journal of Organic Chemistry. 52: 2739-2749. |
0.766 |
|
1987 |
Kuo F, Fuchs PL. Synthesis of a pentacyclic ABCDE bruceantin intermediate Journal of the American Chemical Society. 109: 1122-1128. |
0.361 |
|
1986 |
Kuo F, Fuchs PL. Use of 1-penten-3-one-4-phosphonate as a kinetic ethyl vinyl ketone equivalent in the Robinson annulation reaction Synthetic Communications. 16: 1745-1759. DOI: 10.1080/00397918608057197 |
0.402 |
|
1986 |
Palmer JT, Learn KS, Fuchs PL. Synthesis and facile one-pot aldol/elimination/diels-alder reaction of β-keto-Z-dienylamides as cytochalasin C intermediates Synthetic Communications. 16: 1315-1333. DOI: 10.1080/00397918608056379 |
0.47 |
|
1986 |
Hensel MJ, Palmer JT, Learn KS, Fuchs PL. An intramolecular diels-alder reaction of A Z-diene. Generation of the chiral isoindolone nucleus of Cytochalasin C Synthetic Communications. 16: 1297-1314. DOI: 10.1080/00397918608056378 |
0.426 |
|
1986 |
Hensel MJ, Fuchs PL. A highly selective synthesis of a chiral gamma-amino trisubstituted Z-vinyl ester Synthetic Communications. 16: 1285-1295. DOI: 10.1080/00397918608056377 |
0.438 |
|
1986 |
Fuchs PL, Braish TF. Multiply convergent syntheses via conjugate-addition reactions to cycloalkenyl sulfones Chemical Reviews. 86: 903-917. DOI: 10.1021/Cr00075A012 |
0.39 |
|
1986 |
Hutchinson DK, Fuchs PL. On the chemistry of lithium diallyl cuprate Tetrahedron Letters. 27: 1429-1432. DOI: 10.1016/S0040-4039(00)84277-X |
0.396 |
|
1986 |
Hutchinson DK, Hardinger SA, Fuchs PL. Amine-directed addition of cuprate reagents to cyclopentenyl sulfones Tetrahedron Letters. 27: 1425-1428. DOI: 10.1016/S0040-4039(00)84276-8 |
0.768 |
|
1986 |
HUTCHINSON DK, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 16. On the Chemistry of Lithium Diallyl Cuprate. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198638277 |
0.305 |
|
1986 |
HUTCHINSON DK, HARDINGER SA, FUCHS PL. ChemInform Abstract: Syntheses via Vinyl Sulfones. Part 15. Amine-Directed Addition of Cuprate Reagents to Cyclopentenyl Sulfones. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198638153 |
0.781 |
|
1985 |
Braish TF, Fuchs PL. Synthesis of a chiral bicyclo[4.1.0] allylic nitrile via reductive cyclization of a dienyl nitrile Synthetic Communications. 15: 549-567. DOI: 10.1080/00397918508063841 |
0.411 |
|
1985 |
FRISBEE AR, NANTZ MH, KRAMER GW, FUCHS PL. ChemInform Abstract: LABORATORY AUTOMATION. 1: SYNTHESES VIA VINYL SULFONES. 14. ROBOTIC ORCHESTRATION OF ORGANIC REACTIONS: YIELD OPTIMIZATION VIA AN AUTOMATED SYSTEM WITH OPERATOR-SPECIFIED REACTION SEQUENCES Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198510097 |
0.546 |
|
1984 |
Frisbee AR, Nantz MH, Kramer GW, Fuchs PL. Laboratory automation. 1: syntheses via vinyl sulfones. 14. Robotic orchestration of organic reactions: yield optimization via an automated system with operator-specified reaction sequences Journal of the American Chemical Society. 106: 7143-7145. DOI: 10.1021/Ja00335A047 |
0.586 |
|
1984 |
Suryawanshi SN, Fuchs PL. Cesium fluoride mediated intramolecular conjugate-addition reactions of alpha sulfonyl ester to enones and alpha-chloroenones Tetrahedron Letters. 25: 27-30. DOI: 10.1016/S0040-4039(01)91139-6 |
0.305 |
|
1984 |
Suryawanshi SN, Swenson CJ, Jorgensen WL, Fuchs PL. Torsional effects in the baeyer-villiger oxidation Tetrahedron Letters. 25: 1859-1862. DOI: 10.1016/S0040-4039(01)90060-7 |
0.477 |
|
1984 |
Hamann PR, Toth JE, Fuchs PL. Tandem intramolecular conjugate addition/intramolecular alkylation reactions of substituted vinyl sulfones Journal of Organic Chemistry. 49: 3865-3867. DOI: 10.1002/Chin.198511191 |
0.442 |
|
1984 |
SURYAWANSHI SN, SWENSON CJ, JORGENSEN WL, FUCHS PL. ChemInform Abstract: BRUCEANTIN SUPPORT STUDIES. 7. TORSIONAL EFFECTS IN THE BAEYER-VILLIGER OXIDATION Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198435245 |
0.459 |
|
1984 |
Frisbee AR, Nantz MH, Kramer GW, Fuchs PL. ROBOTIC ORCHESTRATION OF ORGANIC REACTIONS: YIELD OPTIMIZATION VIA AN AUTOMATED SYSTEM WITH OPERATOR-SPECIFIED REACTION SEQUENCES Journal of the American Chemical Society. 106: 7143-7145. |
0.523 |
|
1983 |
Pariza RJ, Kuo F, Fuchs PL. An Improved Procedure for the Synthesis of 4-Oxopimelate-Derived Materials.1 Synthetic Communications. 13: 243-254. DOI: 10.1080/00397918308065996 |
0.402 |
|
1983 |
Donaldson RE, Saddler JC, Byrn S, McKenzie AT, Fuchs PL. Syntheses via vinyl sulfones. 11. A triply convergent total synthesis of L-(-)-prostaglandin E2 The Journal of Organic Chemistry. 48: 2167-2188. DOI: 10.1021/Jo00161A010 |
0.339 |
|
1983 |
Hamann PR, Fuchs PL. Conjugate addition of moderately soft anions to a vinyl sulfone Journal of Organic Chemistry. 48: 914-916. DOI: 10.1021/Jo00154A044 |
0.339 |
|
1982 |
Pyne SG, Spellmeyer DC, Chen S, Fuchs PL. Cytochalasin support studies. 5. Conjugate addition of .beta.-oxo ester dianions to vinyl sulfones: a new procedure for seven-ring annulation. Synthesis of a chiral cytochalasin C intermediate via an intramolecular Diels-Alder reaction of a chiral Z diene Journal of the American Chemical Society. 104: 5728-5740. DOI: 10.1021/ja00385a030 |
0.36 |
|
1982 |
Pyne SG, Hensel MJ, Fuchs PL. Chiral and stereochemical control via intramolecular Diels-Alder reaction of Z dienes Journal of the American Chemical Society. 104: 5719-5728. DOI: 10.1021/Ja00385A029 |
0.367 |
|
1981 |
Ponton J, Helquist P, Conrad PC, Fuchs PL. Six-membered-ring annulation via a conjugate addition-alkylation sequence using functionalized aryllithium reagents and vinyl sulfones The Journal of Organic Chemistry. 46: 118-122. DOI: 10.1021/Jo00314A026 |
0.595 |
|
1981 |
Saddler JC, Fuchs PL. Enantiospecific syntheses of .gamma.-substituted enones: organometallic SN2' conjugate-addition reactions of epoxy vinyl sulfones Journal of the American Chemical Society. 103: 2112-2114. DOI: 10.1021/Ja00398A050 |
0.415 |
|
1981 |
Saddler JC, Donaldson RE, Fuchs PL. Enantioconvergent syntheses of two classes of chiral cyclopentenyl sulfone synthons Journal of the American Chemical Society. 103: 2110-2112. DOI: 10.1021/Ja00398A049 |
0.307 |
|
1981 |
Smith SF, Jorgensen WL, Fuchs PL. PULSAR: a personalized microcomputer-based system for keyword search and retrieval of literature information Journal of Chemical Information and Modeling. 21: 209-213. DOI: 10.1021/Ci00032A006 |
0.383 |
|
1981 |
Suryawanshi S, Fuchs P. Synthesis of gamma-hydroxy enones via persulfate oxidation of dienyl ethers. Tetrahedron Letters. 22: 4201-4204. DOI: 10.1016/S0040-4039(01)82104-3 |
0.335 |
|
1980 |
Pyne SG, Hensel MJ, Byrn SR, McKenzie AT, Fuchs PL. Cytochalasin support studies. 2. Chiral and stereochemical control via an intramolecular Diels-Alder reaction of a (Z)-diene Journal of the American Chemical Society. 102: 5960-5962. DOI: 10.1021/Ja00538A068 |
0.366 |
|
1980 |
Barton DL, Conrad PC, Fuchs PL. Conjugate-addition reactions of highly-functionalized aryl lithium reagents to γ-silyloxy-α,β-unsaturated sulfones: consequences of the structure of the sulfone moiety Tetrahedron Letters. 21: 1811-1814. DOI: 10.1016/S0040-4039(00)92786-2 |
0.364 |
|
1980 |
DAILEY ODJ, FUCHS PL. ChemInform Abstract: SYNTHESIS OF A MODEL FOR THE BCE RING SYSTEM OF BRUCEANTIN. A CAVEAT ON THE CYCLOHEXENE → TRANS DIAXIAL DIOL CONVERSION Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198021241 |
0.311 |
|
1979 |
Clark DA, Fuchs PL. Cytochalasin support studies. Macrocycle synthesis via enolate-assisted, intraannular 1,4-fragmentation reactions Journal of the American Chemical Society. 101: 3567-3576. DOI: 10.1021/Ja00507A022 |
0.424 |
|
1979 |
SADDLER JC, CONRAD PC, FUCHS PL. ChemInform Abstract: SYNTHESIS VIA VINYL SULFONES. 2. CONJUGATE-ADDITION REACTIONS OF ORGANOMETALLIC REAGENTS TO Γ-OXYGENATED-α,β-UNSATURATED SULFONES: CONTROL OF STEREOCHEMISTRY AT THE β-POSITION Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197915184 |
0.326 |
|
1978 |
Hopkins PB, Fuchs PL. Chlorosulfenylation-dehydrochlorination reactions. New and improved methodology for the synthesis of unsaturated aryl sulfides and aryl sulfones Journal of Organic Chemistry. 43: 1208-1217. DOI: 10.1021/Jo00400A041 |
0.675 |
|
1978 |
Clark DA, Bunnell CA, Fuchs PL. Synthetic utilization of the imine moiety. 6. Intramolecular carbon alkylation of oxime anions. Stereospecific generation and rearrangement of nitrosocyclopropanes and nitrosocyclobutanes Journal of the American Chemical Society. 100: 7777-7779. DOI: 10.1021/Ja00492A083 |
0.359 |
|
1977 |
Donaldson RE, Fuchs PL. .alpha.'-Functionalization of .beta.,.gamma.-unsaturated cyclohexenones. Utilization of silyl enol ethers produced from the lithium/ammonia reduction of silyl aryl ethers The Journal of Organic Chemistry. 42: 2032-2034. DOI: 10.1021/Jo00431A055 |
0.305 |
|
1973 |
Vedejs E, Bershas JP, Fuchs PL. .gamma.-Substitution of allyl ylides in the Wittig reaction The Journal of Organic Chemistry. 38: 3625-3627. DOI: 10.1021/Jo00960A044 |
0.664 |
|
1973 |
Vedejs E, Snoble KAJ, Fuchs PL. Phosphorus betaines derived from cycloheptene and cyclooctene oxides. Inversion of cyclooctene The Journal of Organic Chemistry. 38: 1178-1183. DOI: 10.1021/Jo00946A024 |
0.659 |
|
1973 |
Vedejs E, Fuchs PL. Inversion of acyclic olefins by the phosphorus betaine method. Scope and limitations Journal of the American Chemical Society. 95: 822-825. DOI: 10.1021/Ja00784A032 |
0.643 |
|
1973 |
VEDEJS E, SNOBLE KAJ, FUCHS PL. ChemInform Abstract: PHOSPHORBETAINE AUS CYCLOHEPTEN- UND CYCLOOCTENOXIDEN, INVERSION VON CYCLOOCTENEN Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197325388 |
0.635 |
|
1972 |
Corey EJ, Fuchs PL. Homoconjugate addition of organocopper reagents to cyclopropanes and its application to the synthesis of prostanoids. Journal of the American Chemical Society. 94: 4014-5. PMID 5037988 DOI: 10.1021/Ja00766A062 |
0.611 |
|
1972 |
Corey E, Fuchs P. A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′) Tetrahedron Letters. 13: 3769-3772. DOI: 10.1016/S0040-4039(01)94157-7 |
0.446 |
|
1972 |
COREY EJ, FUCHS PL. ChemInform Abstract: EIN NEUES VERFAHREN ZUR UMWANDLUNG VON FORMYL-GRUPPEN IN AETHINYL-GRUPPEN Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/chin.197252188 |
0.46 |
|
1972 |
COREY EJ, FUCHS PL. ChemInform Abstract: HOMOKONJUGIERTE ADDITION VON ORGANOKUPFERREAGENZIEN AN CYCLOPROPANE UND IHRE ANWENDUNG BEI DER SYNTH. VON PROSTANOIDEN Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/chin.197234431 |
0.478 |
|
1971 |
Vedejs E, Fuchs PL. Improved aldehyde synthesis from 1,3-dithianes The Journal of Organic Chemistry. 36: 366-367. DOI: 10.1021/Jo00801A033 |
0.718 |
|
1971 |
Vedejs E, Fuchs PL. Olefin inversion by the phosphorus betaine method Journal of the American Chemical Society. 93: 4070-4072. DOI: 10.1021/Ja00745A054 |
0.632 |
|
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