| Year |
Citation |
Score |
| 2023 |
Jankovic CL, McIntosh KC, Lofstrand VA, West FG. Stereoselective Intramolecular [2 + 2] Trapping of 1,2-Cyclohexadienes: a Route to Rigid, Angularly Fused Tricyclic Scaffolds. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301668. PMID 37352092 DOI: 10.1002/chem.202301668 |
0.376 |
|
| 2019 |
Lofstrand VA, McIntosh KC, Almehmadi YA, West FG. Strain-Activated Diels-Alder Trapping of 1,2-Cyclohexadienes: Intramolecular Capture by Pendent Furans. Organic Letters. PMID 31343882 DOI: 10.1021/Acs.Orglett.9B02085 |
0.486 |
|
| 2018 |
Atienza BJP, Jensen LD, Noton SL, Ansalem AKV, Hobman T, Fearns R, Marchant DJ, West FG. Dual Catalytic Synthesis of Antiviral Compounds Based on Metallocarbene-Azide Cascade Chemistry. The Journal of Organic Chemistry. PMID 29663810 DOI: 10.1021/Acs.Joc.8B00222 |
0.398 |
|
| 2018 |
Gelozia S, Kwon Y, McDonald R, West FG. One-Pot Generation of Bicyclo[3.1.0]hexanols and Cyclohexanones via Double Interrupted Nazarov Reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29444379 DOI: 10.1002/Chem.201800758 |
0.737 |
|
| 2017 |
Hosseini SN, Johnston JR, West FG. Evidence for heterolytic cleavage of a cyclic oxonium ylide: implications for the mechanism of the Stevens [1,2]-shift. Chemical Communications (Cambridge, England). PMID 29125612 DOI: 10.1039/C7Cc07716E |
0.414 |
|
| 2017 |
Fradette RJ, Kang M, West FG. Oxidation-Initiated Cyclizations of Pentadienyl Ethers: An Alternative Entry to the Nazarov Reaction. Angewandte Chemie (International Ed. in English). PMID 28407344 DOI: 10.1002/Anie.201701748 |
0.381 |
|
| 2017 |
Lin R, Cao L, West FG. Medium-Sized Cyclic Ethers via Stevens [1,2]-Shift of Mixed Monothioacetal-Derived Sulfonium Ylides: Application to Formal Synthesis of (+)-Laurencin. Organic Letters. PMID 28102079 DOI: 10.1021/Acs.Orglett.6B03719 |
0.453 |
|
| 2017 |
West F, Wu Y, Lin R. Intercepting the Nazarov Oxyallyl Intermediate with α-Formylvinyl Anion Equivalents to Access Formal Morita–Baylis–Hillman Alkylation Products Synlett. 28: 1486-1490. DOI: 10.1055/S-0036-1588769 |
0.62 |
|
| 2016 |
Schatz DJ, Kwon Y, Scully TW, West FG. Interrupting the Nazarov Cyclization with Bromine. The Journal of Organic Chemistry. 81: 12494-12498. PMID 27978732 DOI: 10.1021/Acs.Joc.6B02350 |
0.73 |
|
| 2016 |
Lofstrand VA, West FG. Efficient Trapping of 1,2-Cyclohexadienes with 1,3-Dipoles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27219685 DOI: 10.1002/Chem.201602201 |
0.474 |
|
| 2016 |
Kumar Kondapi VP, Soueidan OM, Hosseini SN, Jabari N, West FG. Efficient and Easy Access to Optically Pure Tetrasubstituted Tetrahydrofurans via Stereoselective Opening of C2-Symmetric Epoxide and Aziridine Rings European Journal of Organic Chemistry. 2016: 1367-1379. DOI: 10.1002/Ejoc.201501540 |
0.382 |
|
| 2015 |
Kwon Y, Schatz DJ, West FG. 1,4-Diketones from Cross-Conjugated Dienones: Potassium Permanganate-Interrupted Nazarov Reaction. Angewandte Chemie (International Ed. in English). 54: 9940-3. PMID 26138361 DOI: 10.1002/Anie.201503696 |
0.691 |
|
| 2015 |
Patel A, West FG, Houk KN. Reactivity and stereoselectivity of 6π and nazarov electrocyclizations of bridged bicyclic trienes and divinyl ketones. The Journal of Organic Chemistry. 80: 2790-5. PMID 25633968 DOI: 10.1021/Acs.Joc.5B00070 |
0.406 |
|
| 2015 |
Dunbar CR, West FG. Diastereoselective N-quaternization of piperidines Canadian Journal of Chemistry. 93: 468-476. DOI: 10.1139/Cjc-2014-0423 |
0.366 |
|
| 2015 |
Kwon Y, Schatz DJ, West FG. 1,4-Diketones from Cross-conjugated Dienones: Potassium Permanganate-Interrupted Nazarov Reaction Angewandte Chemie - International Edition. DOI: 10.1002/anie.201503696 |
0.673 |
|
| 2014 |
Wu YK, Dunbar CR, McDonald R, Ferguson MJ, West FG. Experimental and computational studies on interrupted Nazarov reactions: exploration of umpolung reactivity at the α-carbon of cyclopentanones. Journal of the American Chemical Society. 136: 14903-11. PMID 25310874 DOI: 10.1021/Ja507638R |
0.608 |
|
| 2014 |
Kwon Y, Scadeng O, McDonald R, West FG. α-Hydroxycyclopentanones via one-pot oxidation of the trimethylaluminum-mediated Nazarov reaction with triplet oxygen. Chemical Communications (Cambridge, England). 50: 5558-60. PMID 24756235 DOI: 10.1039/C4Cc02330G |
0.707 |
|
| 2014 |
Wu YK, West FG. Formal homologous aldol reactions: interrupting the Nazarov cyclization via carboalkoxylation of alkynes. Organic Letters. 16: 2534-7. PMID 24735109 DOI: 10.1021/Ol500914A |
0.593 |
|
| 2014 |
Matier CD, Kwon Y, West FG. Efficient synthesis of bicyclo[6.3.0]undecadienones by Nazarov cyclization/regioselective elimination Canadian Journal of Chemistry. 92: 58-61. DOI: 10.1139/cjc-2013-0456 |
0.72 |
|
| 2014 |
Bott TM, Atienza BJ, West FG. Azide trapping of metallocarbenes: Generation of reactive C-acylimines and domino trapping with nucleophiles Rsc Advances. 4: 31955-31959. DOI: 10.1039/C4Ra06044J |
0.783 |
|
| 2014 |
West FG, Scadeng O, Wu YK, Fradette RJ, Joy S. The Nazarov Cyclization Comprehensive Organic Synthesis: Second Edition. 5: 827-866. DOI: 10.1016/B978-0-08-097742-3.00519-X |
0.399 |
|
| 2014 |
Scadeng O, West FG. Ready access to alkylidenecyclopentenones by Nazarov cyclization/β- elimination of 2-hydroxyalkyl-1,4-dien-3-ones European Journal of Organic Chemistry. 2014: 1860-1865. DOI: 10.1002/Ejoc.201301537 |
0.432 |
|
| 2013 |
Kwon Y, McDonald R, West FG. Organoaluminum-mediated interrupted Nazarov reaction. Angewandte Chemie (International Ed. in English). 52: 8616-9. PMID 23824964 DOI: 10.1002/Anie.201303996 |
0.697 |
|
| 2013 |
Bonderoff SA, Grant TN, West FG, Tremblay M. Nazarov reactions of vinyl cyclopropylamines: an approach to the imino-Nazarov problem. Organic Letters. 15: 2888-91. PMID 23697970 DOI: 10.1021/Ol4012663 |
0.803 |
|
| 2013 |
Joy S, Nakanishi W, West FG. Hydroxylic additives enhance yield and scalability of silicon-directed Nazarov reaction Tetrahedron Letters. 54: 5573-5576. DOI: 10.1016/J.Tetlet.2013.07.139 |
0.436 |
|
| 2013 |
Murphy GK, Stewart C, West FG. Intramolecular generation and rearrangement of oxonium ylides: Methodology studies and their application in synthesis Tetrahedron. 69: 2667-2686. DOI: 10.1016/J.Tet.2013.01.051 |
0.797 |
|
| 2012 |
Wu YK, Niu T, West FG. Construction of α-amido-indanones via formal allenamide hydroacylation-Nazarov cyclization. Chemical Communications (Cambridge, England). 48: 9186-8. PMID 22864235 DOI: 10.1039/C2Cc34644C |
0.599 |
|
| 2012 |
Johnston JR, West FG. Regioselective synthesis of 2-iminooxazinones from dioxinones and carbodiimides Tetrahedron Letters. 53: 5479-5482. DOI: 10.1016/J.Tetlet.2012.07.100 |
0.433 |
|
| 2012 |
Bonderoff SA, West FG, Tremblay M. Superacid-catalyzed Friedel-Crafts cyclization of unactivated alkenes Tetrahedron Letters. 53: 4600-4603. DOI: 10.1016/J.Tetlet.2012.06.082 |
0.786 |
|
| 2011 |
Wu YK, McDonald R, West FG. Homologous Mukaiyama reactions via trapping of the Nazarov intermediate with silyloxyalkenes. Organic Letters. 13: 3584-7. PMID 21699172 DOI: 10.1021/Ol201125H |
0.593 |
|
| 2011 |
Stewart C, McDonald R, West FG. Expedient route to the tigliane-daphnane skeleton via oxonium ylide [1,2]-shift. Organic Letters. 13: 720-3. PMID 21241059 DOI: 10.1021/Ol102953S |
0.63 |
|
| 2011 |
Scadeng O, Ferguson MJ, West FG. Intermolecular [3 + 3]-cycloadditions of azides with the Nazarov intermediate. Organic Letters. 13: 114-7. PMID 21126097 DOI: 10.1021/Ol102651K |
0.446 |
|
| 2011 |
Rieder CJ, Winberg KJ, West FG. Olefination of α,α'-divinyl ketones through catalytic Meyer-Schuster rearrangement. The Journal of Organic Chemistry. 76: 50-6. PMID 21105713 DOI: 10.1021/Jo101497F |
0.429 |
|
| 2011 |
Bott TM, West FG. Preparation and synthetic applications of azetidines Heterocycles. 84: 223-264. DOI: 10.3987/Rev-11-Sr(P)9 |
0.756 |
|
| 2010 |
Wu YK, West FG. Brønsted acid-mediated Nazarov cyclization of vinylallenes. The Journal of Organic Chemistry. 75: 5410-3. PMID 20670041 DOI: 10.1021/Jo101112T |
0.569 |
|
| 2010 |
Rieder CJ, Fradette RJ, West FG. Hetero aromatic trapping of tricyclic 2-oxidocyclopentenyl cations: A surprisingly efficient example of intermolecular interrupted nazarov reaction Heterocycles. 80: 1413-1427. DOI: 10.3987/Com-09-S(S)132 |
0.352 |
|
| 2010 |
Giese S, Kastrup L, Stiens D, West FG. ChemInform Abstract: Intermolecular Trapping of the Nazarov Intermediate: Domino Electrocyclization/[3 + 2] Cycloadditions with Allylsilanes. Cheminform. 31: no-no. DOI: 10.1002/chin.200034161 |
0.32 |
|
| 2010 |
AMANN CM, FISHER PV, PUGH ML, WEST FG. ChemInform Abstract: Medium-Sized Carbocycles and Ethers from 4-Pyrones: A Photocyclization - Fragmentation Approach. Cheminform. 29: no-no. DOI: 10.1002/chin.199833128 |
0.519 |
|
| 2009 |
Grant TN, Rieder CJ, West FG. Interrupting the Nazarov reaction: domino and cascade processes utilizing cyclopentenyl cations. Chemical Communications (Cambridge, England). 5676-88. PMID 19774236 DOI: 10.1039/B908515G |
0.488 |
|
| 2009 |
Rieder CJ, Winberg KJ, West FG. Cyclization of cross-conjugated trienes: the vinylogous Nazarov reaction. Journal of the American Chemical Society. 131: 7504-5. PMID 19435345 DOI: 10.1021/Ja9023226 |
0.429 |
|
| 2009 |
Bott TM, Vanecko JA, West FG. One-carbon ring expansion of azetidines via ammonium ylide [1,2]-shifts: a simple route to substituted pyrrolidines. The Journal of Organic Chemistry. 74: 2832-6. PMID 19265415 DOI: 10.1021/Jo9001323 |
0.791 |
|
| 2009 |
Li L, Bender JA, West FG. Diastereocontrol in [4+4]-photocycloadditions of pyran-2-ones: effect of ring substituents and chiral ketal Tetrahedron Letters. 50: 1188-1192. DOI: 10.1016/J.Tetlet.2008.12.117 |
0.439 |
|
| 2009 |
Wilson AM, Rheingold AL, Waldman TE, Klein M, West FG, Ernst RD. Fused ring systems derived from reactions of half-open titanocenes with diynes: Syntheses, characterization, cage rearrangements, and structural studies Journal of Organometallic Chemistry. 694: 1112-1121. DOI: 10.1016/J.Jorganchem.2008.09.008 |
0.433 |
|
| 2009 |
Nuss JM, West FG. The Photochemistry of Dienes and Polyenes: Application to the Synthesis of Complex Molecules Patai's Chemistry of Functional Groups. 263-324. DOI: 10.1002/9780470682531.Pat0103 |
0.453 |
|
| 2008 |
Li L, Chase CE, West FG. Cyclooctatrienes from pyran-2-ones via a tandem [4+4]-photocycloaddition/decarboxylation process. Chemical Communications (Cambridge, England). 4025-7. PMID 18758614 DOI: 10.1039/B806871B |
0.381 |
|
| 2008 |
Grant TN, Benson CL, West FG. Ring expansion of lactones and lactams via propiolate 1-carbon intercalation. Organic Letters. 10: 3985-8. PMID 18707105 DOI: 10.1021/Ol8014682 |
0.472 |
|
| 2008 |
Li L, McDonald R, West FG. Concise route to triquinanes from pyran-2-ones. Organic Letters. 10: 3733-6. PMID 18683940 DOI: 10.1021/Ol8013683 |
0.365 |
|
| 2008 |
Rieder CJ, Fradette RJ, West FG. Construction of aryl-substituted triquinanes through the interrupted Nazarov reaction. Chemical Communications (Cambridge, England). 1572-4. PMID 18354803 DOI: 10.1039/B800800K |
0.449 |
|
| 2007 |
Song D, Rostami A, West FG. Domino electrocyclization/azide-capture/schmidt rearrangement of dienones: one-step synthesis of dihydropyridones from simple building blocks. Journal of the American Chemical Society. 129: 12019-22. PMID 17824702 DOI: 10.1021/Ja071041Z |
0.515 |
|
| 2007 |
Grant TN, West FG. Interrupted nazarov reactions using dichlorocyclopropanes: a novel mode of arene trapping. Organic Letters. 9: 3789-92. PMID 17705503 DOI: 10.1021/Ol7015669 |
0.437 |
|
| 2007 |
Benson CL, West FG. Highly stereoselective 6pi electrocyclization of bridged bicyclic 1,3,5-trienes. Organic Letters. 9: 2545-8. PMID 17530764 DOI: 10.1021/Ol070924S |
0.387 |
|
| 2007 |
Rostami A, Wang Y, Arif AM, McDonald R, West FG. Intramolecular azide trapping of the Nazarov intermediate: formation of peroxy-bridged indolizidinones via a deep-seated rearrangement and aerobic oxidation. Organic Letters. 9: 703-6. PMID 17256871 DOI: 10.1021/Ol070053M |
0.435 |
|
| 2007 |
Vanecko JA, West FG. Survey of chemical syntheses of the pyrrolizidine alkaloids turneforcidine and platynecine Heterocycles. 74: 125-143. DOI: 10.3987/Rev-07-Sr(W)5 |
0.373 |
|
| 2007 |
Mahmoud B, West FG. Efficient intermolecular 3+2 trapping of the Nazarov intermediate with vinyl sulfides Tetrahedron Letters. 48: 5091-5094. DOI: 10.1016/J.Tetlet.2007.05.093 |
0.47 |
|
| 2006 |
Liu X, West FG. Construction of fused bis(pyran) units from enones via a hydrosilylation-dihydroxylation-acetalization-reduction sequence. Chemical Communications (Cambridge, England). 5036-8. PMID 17146519 DOI: 10.1039/B610886E |
0.36 |
|
| 2006 |
Murphy GK, West FG. [1,2]- or [2,3]-rearrangement of onium ylides of allyl and benzyl ethers and sulfides via in situ-generated iodonium ylides. Organic Letters. 8: 4359-61. PMID 16956226 DOI: 10.1021/Ol061772O |
0.802 |
|
| 2006 |
Song D, McDonald R, West FG. Diastereoselective [4 + 4]-photocycloaddition reactions of pyran-2-ones: rapid access to functionalized 5-8-5 skeletons. Organic Letters. 8: 4075-8. PMID 16928077 DOI: 10.1021/Ol061576H |
0.449 |
|
| 2006 |
Grant TN, West FG. A new approach to the nazarov reaction via sequential electrocyclic ring opening and ring closure. Journal of the American Chemical Society. 128: 9348-9. PMID 16848467 DOI: 10.1021/Ja063421A |
0.503 |
|
| 2006 |
Murphy GK, Marmsäter FP, West FG. Polycyclic oxonium ylides - Use of cyclic acetals as convenient scaffolds in the construction of fused bicyclic compounds containing a medium ring Canadian Journal of Chemistry. 84: 1470-1486. DOI: 10.1139/V06-111 |
0.765 |
|
| 2006 |
Vanecko JA, Wan H, West FG. Recent advances in the Stevens rearrangement of ammonium ylides. Application to the synthesis of alkaloid natural products Tetrahedron. 62: 1043-1062. DOI: 10.1016/J.Tet.2005.09.123 |
0.358 |
|
| 2005 |
Giese S, Mazzola RD, Amann CM, Arif AM, West FG. Unexpected participation of an unconjugated olefin during Nazarov cyclization of bridged bicyclic dienones. Angewandte Chemie (International Ed. in English). 44: 6546-9. PMID 16173000 DOI: 10.1002/Anie.200501737 |
0.33 |
|
| 2005 |
Vanecko JA, West FG. Ring expansion of azetidinium ylides: rapid access to the pyrrolizidine alkaloids turneforcidine and platynecine. Organic Letters. 7: 2949-52. PMID 15987177 DOI: 10.1021/Ol050915O |
0.52 |
|
| 2005 |
Mazzola RD, White TD, Vollmer-Snarr HR, West FG. Stereoselective Nazarov cyclizations of bridged bicyclic dienones. Organic Letters. 7: 2799-801. PMID 15957950 DOI: 10.1021/Ol051169Q |
0.459 |
|
| 2005 |
Murphy GK, West FG. Hydrazulene ring systems via heteroatom-assisted [1,2]-shift of oxonium and sulfonium ylides. Organic Letters. 7: 1801-4. PMID 15844910 DOI: 10.1021/Ol050396P |
0.684 |
|
| 2005 |
White TD, West FG. Halide trapping of the Nazarov intermediate in strained polycyclic systems: A new interrupted Nazarov reaction Tetrahedron Letters. 46: 5629-5632. DOI: 10.1016/J.Tetlet.2005.06.101 |
0.434 |
|
| 2004 |
Marmsäter FP, Vanecko JA, West FG. Catalyst and ring size effects on periselectivity of oxonium ylide rearrangements. Organic Letters. 6: 1657-60. PMID 15128260 DOI: 10.1021/Ol049493T |
0.31 |
|
| 2004 |
Mazzola RD, Giese S, Benson CL, West FG. Improved yields with added copper(I) salts in carbonylative stille couplings of sterically hindered vinylstannanes. The Journal of Organic Chemistry. 69: 220-3. PMID 14703405 DOI: 10.1021/Jo034788Q |
0.378 |
|
| 2004 |
Browder CC, Marmsäter FP, West FG. Efficient construction of benzohydrindenones from aryltrienones via domino Nazarov electrocyclization - Electrophilic aromatic substitution Canadian Journal of Chemistry. 82: 375-385. DOI: 10.1139/V03-203 |
0.486 |
|
| 2004 |
Yungai A, West FG. Convenient route to centro-substituted triquinacene skeletons via the interrupted Nazarov reaction Tetrahedron Letters. 45: 5445-5448. DOI: 10.1016/J.Tetlet.2004.05.072 |
0.524 |
|
| 2003 |
Marmsäter FP, Murphy GK, West FG. Cyclooctanoid ring systems from mixed acetals via heteroatom-assisted [1,2]-shift of oxonium ylides. Journal of the American Chemical Society. 125: 14724-5. PMID 14640645 DOI: 10.1021/Ja0387249 |
0.671 |
|
| 2003 |
Wang Y, Schill BD, Arif AM, West FG. Formal intermolecular 4 + 4 approach to cyclooctanoids: 4 + 3 capture of the Nazarov oxyallyl intermediate with simple 1,3-dienes. Organic Letters. 5: 2747-50. PMID 12868905 DOI: 10.1021/Ol034985B |
0.448 |
|
| 2003 |
Glaeske KW, Naidu BN, West FG. Stereoselective formation and rearrangement of morpholinium ylides derived from copper carbenoids Tetrahedron Asymmetry. 14: 917-920. DOI: 10.1016/S0957-4166(03)00095-8 |
0.365 |
|
| 2002 |
Marmsäter FP, West FG. New efficient iterative approaches to polycyclic ethers. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 4346-53. PMID 12355522 DOI: 10.1002/1521-3765(20021004)8:19<4346::Aid-Chem4346>3.0.Co;2-S |
0.421 |
|
| 2002 |
Vanecko JA, West FG. A novel, stereoselective silyl-directed Stevens [1,2]-shift of ammonium ylides. Organic Letters. 4: 2813-6. PMID 12182562 DOI: 10.1021/Ol025951R |
0.467 |
|
| 2002 |
Wang Y, West FG. A convenient method for the synthesis of terminal (E)-1,3-dienes Synthesis. 99-103. DOI: 10.1055/S-2002-19297 |
0.421 |
|
| 2002 |
Marmsäter FP, Vanecko JA, West FG. Cyclic oxonium ylides: Building blocks for iterative synthesis of polycyclic ethers Tetrahedron. 58: 2027-2040. DOI: 10.1016/S0040-4020(02)00051-0 |
0.49 |
|
| 2001 |
Browder CC, Marmsäter FP, West FG. Highly efficient trapping of the Nazarov intermediate with substituted arenes. Organic Letters. 3: 3033-5. PMID 11554836 DOI: 10.1021/Ol010159W |
0.5 |
|
| 2001 |
Marmsäter FP, West FG. Iterative approach to polycyclic ethers based on stereoselective oxonium ylide [2,3]-shifts. Journal of the American Chemical Society. 123: 5144-5. PMID 11457364 DOI: 10.1021/Ja015872V |
0.31 |
|
| 2001 |
Smeltzer CC, Cannon MJ, Pinson PR, Munger JD, West FG, Grissom CB. Synthesis and characterization of fluorescent cobalamin (CobalaFluor) derivatives for imaging. Organic Letters. 3: 799-801. PMID 11263885 DOI: 10.1021/Ol006825V |
0.329 |
|
| 2001 |
Fleming M, Fisher PV, Gunawardena GU, Jin Y, Zhang C, Zhang W, Arif AM, West FG. Solvent trapping of photochemically generated pyran-4-one-derived oxyallyls: A convenient cyclopentannulation method Synthesis. 1268-1274. DOI: 10.1055/S-2001-15067 |
0.757 |
|
| 2000 |
Giese S, Kastrup L, Stiens D, West FG. Intermolecular Trapping of the Nazarov Intermediate: Domino Electrocyclization/ Angewandte Chemie (International Ed. in English). 39: 1970-1973. PMID 10940999 DOI: 10.1002/1521-3773(20000602)39:11<1970::Aid-Anie1970>3.0.Co;2-B |
0.378 |
|
| 2000 |
Giese S, West FG. Ionic hydrogenation of oxyallyl intermediates: The reductive nazarov cyclization Tetrahedron. 56: 10221-10228. DOI: 10.1016/S0040-4020(00)00866-8 |
0.443 |
|
| 2000 |
Wilson AM, West FG, Rheingold AL, Ernst RD. Synthesis, characterization, and organic chemistry of an edge-bridged half-open titanocene Inorganica Chimica Acta. 300: 65-72. DOI: 10.1016/S0020-1693(99)00455-7 |
0.326 |
|
| 1999 |
Fleming M, Basta R, Fisher PV, Mitchell S, West FG. Synthesis of Bridged Bicyclic Ethers and Fused Oxetanes from Pyran-4-ones via Tandem Solvent Trapping and Norrish Type II Cyclization(1). The Journal of Organic Chemistry. 64: 1626-1629. PMID 11674228 DOI: 10.1021/Jo9821224 |
0.661 |
|
| 1999 |
Glaeske KW, West FG. Chirality transfer from carbon to nitrogen to carbon via cyclic ammonium ylides Organic Letters. 1: 31-33. DOI: 10.1021/Ol9905349 |
0.341 |
|
| 1999 |
Fleming M, Basta R, Fisher PV, Mitchell S, West FG. Synthesis of bridged bicyclic ethers and fused oxetanes from pyran-4- ones via tandem solvent trapping and norfish type II cyclization Journal of Organic Chemistry. 64: 1626-1629. DOI: 10.1021/jo9821224 |
0.599 |
|
| 1999 |
Bender JA, Arif AM, West FG. Nazarov-initiated diastereoselective cascade polycyclization of aryltrienones [20] Journal of the American Chemical Society. 121: 7443-7444. DOI: 10.1021/Ja991215F |
0.345 |
|
| 1999 |
Wang Y, Arif AM, West FG. A novel cycloisomerization of tetraenones: 4+3 Trapping of the Nazarov oxyallyl intermediate [11] Journal of the American Chemical Society. 121: 876-877. DOI: 10.1021/Ja9837001 |
0.363 |
|
| 1998 |
Bender JA, Blize AE, Browder CC, Giese S, West FG. Highly Diastereoselective Cycloisomerization of Acyclic Trienones. The Interrupted Nazarov Reaction. The Journal of Organic Chemistry. 63: 2430-2431. PMID 11672099 DOI: 10.1021/Jo9803030 |
0.417 |
|
| 1998 |
Amann CM, Fisher PV, Pugh ML, West FG. Medium-Sized Carbocycles and Ethers from 4-Pyrones: A Photocyclization− Fragmentation Approach1 The Journal of Organic Chemistry. 63: 2806-2807. DOI: 10.1021/Jo980274T |
0.549 |
|
| 1998 |
Giese S, West FG. The reductive Nazarov cyclization Tetrahedron Letters. 39: 8393-8396. DOI: 10.1016/S0040-4039(98)01934-0 |
0.439 |
|
| 1998 |
Tester RW, West FG. Medium ring ethers via [1,2]-shift of acetal-derived oxonium ylides Tetrahedron Letters. 39: 4631-4634. DOI: 10.1016/S0040-4039(98)00856-9 |
0.518 |
|
| 1998 |
Bender JA, Daves S, West FG. 1,3-dioxolan-2-ylium cations from acylfurans: Conversion of furyl ketones to esters under nonoxidative conditions Tetrahedron Letters. 39: 2051-2054. DOI: 10.1016/S0040-4039(98)00185-3 |
0.455 |
|
| 1997 |
Gunawardena GU, Arif AM, West FG. Tandem enamine Michael additions to 4-(mesyloxy)cyclopentenones: Bridged tricyclic skeletons via a net [3 + 2] construction Journal of the American Chemical Society. 119: 2066-2067. DOI: 10.1021/Ja963978Y |
0.768 |
|
| 1997 |
Naidu BN, West FG. A short, enantioselective synthesis of (-)-epilupinine from proline via a spirocyclic ammonium ylide Tetrahedron. 53: 16565-16574. DOI: 10.1016/S0040-4020(97)01037-5 |
0.311 |
|
| 1996 |
Stork G, West F, Lee HY, Isaacs RCA, Manabe S. The total synthesis of a natural cardenolide: (+)-digitoxigenin Journal of the American Chemical Society. 118: 10660-10661. DOI: 10.1021/Ja962163M |
0.639 |
|
| 1995 |
Wilson AM, West FG, Arif AM, Ernst RD. Unprecedented diastereoselective addition reactions of 6,6-dimethylcyclohexadienyl titanium complexes to aldehydes and ketones Journal of the American Chemical Society. 117: 8490-8491. DOI: 10.1021/Ja00137A035 |
0.412 |
|
| 1995 |
Chase CE, Jarstfer MB, Arif AM, West FG. Unexpected and efficient photochemical rearrangement of 6-hydroxyethylpyran-2-ones to 4-AIkylidene-5,6-dihydropyrans Tetrahedron Letters. 36: 8531-8534. DOI: 10.1016/0040-4039(95)01828-6 |
0.406 |
|
| 1994 |
West FG, Naidu BN, Tester RW. Profound catalyst effects in the generation and reactivity of carbenoid-derived cyclic ylides Journal of Organic Chemistry. 59: 6892-6894. DOI: 10.1021/Jo00102A007 |
0.344 |
|
| 1994 |
West FG, Naidu BN. Applications of Stevens [1,2]-shifts of cyclic ammonium ylides. A route to morpholin-2-ones Journal of Organic Chemistry. 59: 6051-6056. DOI: 10.1021/Jo00099A041 |
0.323 |
|
| 1994 |
West FG, Amann CM, Fisher PV. Intramolecular carboxylic acid trapping of pyran-4-one derived zwitterions: A novel synthesis of fused bicyclic lactones Tetrahedron Letters. 35: 9653-9656. DOI: 10.1016/0040-4039(94)88351-3 |
0.693 |
|
| 1993 |
West FG, Glaeske KW, Naidu BN. One-step synthesis of tertiary α-amino ketones and α-amino esters from amines and diazocarbonyl compounds Synthesis. 977-980. DOI: 10.1055/S-1993-25984 |
0.391 |
|
| 1993 |
West FG, Eberlein TH, Tester RW. O-bridged medium sized rings via bicyclic oxonium ylides Journal of the Chemical Society, Perkin Transactions 1. 2857-2859. DOI: 10.1039/P19930002857 |
0.363 |
|
| 1993 |
West FG, Koch DJ. Novel bicyclic oxazolines via nitrile capture of photochemically generated oxyallyl zwitterions Journal of the Chemical Society, Chemical Communications. 1681-1682. DOI: 10.1039/C39930001681 |
0.427 |
|
| 1993 |
West FG, Hartke-Karger C, Koch DJ, Kuehn CE, Arif AM. Intramolecular [4 + 3]-Cycloadditions of photochemically generated oxyallyl zwitterions: A route to functionalized cyclooctanoid skeletons Journal of Organic Chemistry. 58: 6795-6803. DOI: 10.1021/Jo00076A047 |
0.353 |
|
| 1993 |
West FG, Gunawardena GU. Pseudocine substitution via internal delivery. Formal cyclopentadienone-ketone Michael adducts from 4-hydroxycyclopentenones Journal of Organic Chemistry. 58: 5043-5044. DOI: 10.1021/Jo00071A008 |
0.784 |
|
| 1993 |
West FG, Willoughby DW. Intramolecular arene trapping of pyran-4-one derived zwitterions: A two-step synthesis of tetrahydrobenz[e]inden-1-ones Journal of Organic Chemistry. 58: 3796-3797. DOI: 10.1021/Jo00067A007 |
0.467 |
|
| 1993 |
West FG, Chase CE, Arif AM. Intramolecular [4 + 4]-photocycloadditions of 2-pyrones: An efficient approach to cyclooctanoid construction Journal of Organic Chemistry. 58: 3794-3795. DOI: 10.1021/Jo00067A006 |
0.433 |
|
| 1993 |
West FG, Gunawardena GU. Pseudocine substitution of 4-(mesyloxy)-2-cyclopentenones: An efficient route to 2,4-disubstituted 2-cyclopentenones Journal of Organic Chemistry. 58: 2402-2406. DOI: 10.1021/Jo00061A010 |
0.442 |
|
| 1993 |
West FG, Fisher PV, Arif AM. Intramolecular alkene trapping of pyran-4-one-derived zwitterions: A novel synthesis of diquinanes and hydrindans Journal of the American Chemical Society. 115: 1595-1597. DOI: 10.1021/Ja00057A066 |
0.681 |
|
| 1993 |
West FG, Naidu BN. New route to substituted piperidines via the stevens [1,2]-shift of ammonium ylides Journal of the American Chemical Society. 115: 1177-1178. DOI: 10.1021/Ja00056A069 |
0.37 |
|
| 1993 |
West FG, Fisher PV, Gunawardena GU, Mitchell S. Photochemical ring-contraction of fused bicyclic 4-pyrones: A novel 2-step cyclopentannulation approach Tetrahedron Letters. 34: 4583-4586. DOI: 10.1016/S0040-4039(00)60630-5 |
0.799 |
|
| 1992 |
Eberlein TH, West FG, Tester RW. The Stevens [1,2]-shift of oxonium ylides: A route to substituted tetrahydrofuranones Journal of Organic Chemistry. 57: 3479-3482. DOI: 10.1021/Jo00038A043 |
0.382 |
|
| 1990 |
West FG, Fisher PV, Willoughby CA. The photochemistry of pyran-4-ones: Intramolecular trapping of the zwitterionic intermediate with pendant hydroxyl groups Journal of Organic Chemistry. 55: 5936-5938. DOI: 10.1021/Jo00311A008 |
0.677 |
|
| 1986 |
Vedejs E, West FG. Ylides by the desilylation of .alpha.-silyl onium salts Chemical Reviews. 86: 941-955. DOI: 10.1021/Cr00075A014 |
0.485 |
|
| 1986 |
Vedejs E, West FG. Ylides by the desilylation of α-silyl onium salts Chemical Reviews. 86: 941-955. |
0.467 |
|
| 1985 |
Vedejs E, Larsen S, West FG. Nonstabilized imidate ylides by the desilylation method: A route to the pyrrolizidine alkaloids retronecine and indicine Journal of Organic Chemistry. 50: 2170-2174. DOI: 10.1002/Chin.198547317 |
0.534 |
|
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