| Year |
Citation |
Score |
| 2019 |
da Silva Gomes R, Corey EJ. A Method for the Catalytic Enantioselective Synthesis of Chiral α-Azido and α-Amino Ketones from Racemic α-Bromo Ketones, and Its Generalization to the Formation of Bonds to C, O, and S. Journal of the American Chemical Society. PMID 31821754 DOI: 10.1021/Jacs.9B12315 |
0.358 |
|
| 2018 |
Han Y, Corey EJ. Method for the Direct Enantioselective Synthesis of Chiral Primary α-Amino Ketones by Catalytic α-Amination. Organic Letters. PMID 30576160 DOI: 10.1021/Acs.Orglett.8B03733 |
0.748 |
|
| 2018 |
Depa SR, Corey EJ. Enantioselective Conversion of Oligoprenol Derivatives to Macro-cycles in the Germacrene, Cembrene and 18-Membered Cyclic Sester-terpene Series. Journal of the American Chemical Society. PMID 30466258 DOI: 10.1021/Jacs.8B10522 |
0.372 |
|
| 2018 |
da Silva Gomes R, Reddy KM, Corey EJ. Synthesis of Chiral Cyclic Alcohols from Chiral Epoxides by H or N Substitution with Frontside Displacement. Organic Letters. PMID 30256646 DOI: 10.1021/Acs.Orglett.8B02822 |
0.372 |
|
| 2018 |
Remarchuk T, Corey EJ. Stereodivergent synthesis of novel chiral C2-symmetric bis-trifluoromethyl-2-oxazolidinones Tetrahedron Letters. 59: 2256-2259. DOI: 10.1016/J.Tetlet.2018.04.072 |
0.379 |
|
| 2017 |
Breitler S, Han Y, Corey EJ. Highly Diastereoselective Cationic Cyclization Reactions Convert a Common Monocyclic Enone to Bicyclic Precursors for the Synthesis of Retigeranic Acids A and B. Organic Letters. 19: 6686-6687. PMID 29192787 DOI: 10.1021/Acs.Orglett.7B03412 |
0.755 |
|
| 2017 |
Han Y, Mahender Reddy K, Corey EJ. Simple Enantioselective Syntheses of (2R,6R)-Hydroxynorketamine and Related Potential Rapid-Onset Antidepressants. Organic Letters. PMID 28892391 DOI: 10.1021/Acs.Orglett.7B02498 |
0.718 |
|
| 2017 |
Mahender Reddy K, Thirupathi B, Corey EJ. Useful Applications of Enantioselective (4 + 2)-Cycloaddition Reactions to the Synthesis of Chiral 1,2-Amino Alcohols, 1,2-Diamines, and β-Amino Acids. Organic Letters. PMID 28858513 DOI: 10.1021/Acs.Orglett.7B02437 |
0.407 |
|
| 2017 |
Bhimireddy E, Corey EJ. Method for Highly Enantioselective Ligation of Two Chiral C(sp(3)) Stereocenters. Journal of the American Chemical Society. PMID 28759226 DOI: 10.1021/Jacs.7B07366 |
0.357 |
|
| 2017 |
Vemula R, Wilde NC, Goreti R, Corey EJ. A New, Short, and Stereocontrolled Synthesis of C2-Symmetric 1,2-Diamines. Organic Letters. PMID 28696724 DOI: 10.1021/Acs.Orglett.7B01768 |
0.801 |
|
| 2016 |
Han Y, Breitler S, Zheng SL, Corey EJ. Enantioselective Conversion of Achiral Cyclohexadienones to Chiral Cyclohexenones by Desymmetrization. Organic Letters. 18: 6172-6175. PMID 27934349 DOI: 10.1021/Acs.Orglett.6B03186 |
0.747 |
|
| 2016 |
Thirupathi B, Breitler S, Mahender Reddy K, Corey EJ. Acceleration of Enantioselective Cycloadditions Catalyzed by Second-Generation Chiral Oxazaborolidinium Triflimidates by Biscoordinating Lewis Acids. Journal of the American Chemical Society. PMID 27530433 DOI: 10.1021/Jacs.6B08018 |
0.369 |
|
| 2016 |
Mahender Reddy K, Bhimireddy E, Thirupathi B, Breitler S, Yu S, Corey EJ. Cationic Chiral Fluorinated Oxazaborolidines. More Potent, Second Generation Catalysts for Highly Enantioselective Cycloaddition Reactions. Journal of the American Chemical Society. PMID 26812167 DOI: 10.1021/Jacs.6B00100 |
0.377 |
|
| 2015 |
Rajendar G, Corey EJ. A systematic study of functionalized oxiranes as initiating groups for cationic polycyclization reactions. Journal of the American Chemical Society. 137: 5837-44. PMID 25871500 DOI: 10.1021/Jacs.5B03229 |
0.402 |
|
| 2014 |
Surendra K, Corey EJ. Diiodoindium(III) cation, InI₂⁺, a potent yneophile. Generation and application to cationic cyclization by selective π-activation of C≡C. Journal of the American Chemical Society. 136: 10918-20. PMID 25095905 DOI: 10.1021/Ja506502P |
0.33 |
|
| 2014 |
Surendra K, Rajendar G, Corey EJ. Useful catalytic enantioselective cationic double annulation reactions initiated at an internal π-bond: method and applications. Journal of the American Chemical Society. 136: 642-5. PMID 24359428 DOI: 10.1021/Ja4125093 |
0.346 |
|
| 2013 |
Newhouse TR, Kaib PS, Gross AW, Corey EJ. Versatile approaches for the synthesis of fused-ring γ-lactones utilizing cyclopropane intermediates. Organic Letters. 15: 1591-3. PMID 23470216 DOI: 10.1021/Ol400362T |
0.815 |
|
| 2013 |
Corey EJ, Kurti L. Enantioselective Chemical Synthesis: Methods, Logic, and Practice Enantioselective Chemical Synthesis: Methods, Logic, and Practice. 1-328. |
0.605 |
|
| 2012 |
Newhouse TR, Li X, Blewett MM, Whitehead CM, Corey EJ. A tetradentate ligand for the enantioselective Ti(IV)-promoted oxidation of sulfides to sulfoxides: origin of enantioselectivity. Journal of the American Chemical Society. 134: 17354-7. PMID 23046346 DOI: 10.1021/Ja305991K |
0.767 |
|
| 2012 |
Surendra K, Corey EJ. Highly enantioselective proton-initiated polycyclization of polyenes. Journal of the American Chemical Society. 134: 11992-4. PMID 22780430 DOI: 10.1021/Ja305851H |
0.363 |
|
| 2011 |
Qiu WW, Surendra K, Yin L, Corey EJ. Selective formation of six-membered oxa- and carbocycles by the In(III)-activated ring closure of acetylenic substrates. Organic Letters. 13: 5893-5. PMID 21992657 DOI: 10.1021/Ol202621G |
0.323 |
|
| 2011 |
Surendra K, Qiu W, Corey EJ. A powerful new construction of complex chiral polycycles by an indium(III)-catalyzed cationic cascade. Journal of the American Chemical Society. 133: 9724-6. PMID 21644499 DOI: 10.1021/Ja204142N |
0.379 |
|
| 2011 |
Mukherjee S, Corey EJ. ChemInform Abstract: Enantioselective Synthesis Based on Catalysis by Chiral Oxazaborolidinium Cations Cheminform. 42: no-no. DOI: 10.1002/chin.201127221 |
0.307 |
|
| 2010 |
Shenvi RA, Corey EJ. Synthetic access to bent polycycles by cation-pi cyclization. Organic Letters. 12: 3548-51. PMID 20670018 DOI: 10.1021/Ol101410G |
0.752 |
|
| 2010 |
Brown MK, Blewett MM, Colombe JR, Corey EJ. Mechanism of the enantioselective oxidation of racemic secondary alcohols catalyzed by chiral Mn(III)-salen complexes. Journal of the American Chemical Society. 132: 11165-70. PMID 20666410 DOI: 10.1021/Ja103103D |
0.669 |
|
| 2010 |
Mukherjee S, Scopton AP, Corey EJ. Enantioselective pathway for the synthesis of laurenditerpenol. Organic Letters. 12: 1836-8. PMID 20337419 DOI: 10.1021/Ol1004802 |
0.414 |
|
| 2010 |
Gao X, Singh RP, Corey EJ. Enantioselective synthesis of a chiral C(3)-symmetric bridgehead amine. Organic Letters. 12: 1812-4. PMID 20329741 DOI: 10.1021/Ol100426M |
0.683 |
|
| 2010 |
Xiong Z, Busch R, Corey EJ. A short total synthesis of (+)-omaezakianol via an epoxide-initiated cationic cascade reaction. Organic Letters. 12: 1512-4. PMID 20218639 DOI: 10.1021/Ol100213E |
0.428 |
|
| 2010 |
Mukherjee S, Corey EJ. [4 + 2] Cycloaddition reactions catalyzed by a chiral oxazaborolidinium cation. Reaction rates and diastereo-, regio-, and enantioselectivity depend on whether both bonds are formed simultaneously. Organic Letters. 12: 1024-7. PMID 20131879 DOI: 10.1021/Ol100032U |
0.321 |
|
| 2010 |
Mukherjee S, Corey EJ. Highly enantioselective Diels-Alder reactions of maleimides catalyzed by activated chiral oxazaborolidines. Organic Letters. 12: 632-5. PMID 20063859 DOI: 10.1021/Ol902865D |
0.366 |
|
| 2010 |
Larionov OV, Corey EJ. Ni(II)-catalyzed enantioselective conjugate addition of acetylenes to alpha,beta-enones. Organic Letters. 12: 300-2. PMID 20000753 DOI: 10.1021/Ol902643W |
0.606 |
|
| 2010 |
Brown MK, Corey EJ. Catalytic enantioselective formation of chiral-bridged dienes which are themselves ligands for enantioselective catalysis. Organic Letters. 12: 172-5. PMID 19947622 DOI: 10.1021/Ol9025793 |
0.459 |
|
| 2010 |
COREY EJ, HELAL CJ. ChemInform Abstract: Asymmetric Synthesis of (S)-Carbinoxamine. New Aspects of Oxazaborolidine-Catalyzed Enantioselective Carbonyl Reduction. Cheminform. 27: no-no. DOI: 10.1002/chin.199645055 |
0.314 |
|
| 2010 |
COREY EJ, WU LI. ChemInform Abstract: Enantioselective Total Synthesis of Miroestrol. Cheminform. 25: no-no. DOI: 10.1002/chin.199404235 |
0.335 |
|
| 2010 |
COREY EJ, SODEOKA M. ChemInform Abstract: An Efficient System for Epoxide-Initiated Cation - Olefin Cyclization. Cheminform. 23: no-no. DOI: 10.1002/chin.199230078 |
0.492 |
|
| 2010 |
COREY EJ, CHENG X, CIMPRICH KA. ChemInform Abstract: 1-Mesityl-2,2,2-trifluoroethanol. An Outstanding New Chiral Controller for Catalyzed Diels-Alder Reactions. Cheminform. 23: no-no. DOI: 10.1002/chin.199229068 |
0.638 |
|
| 2009 |
Surendra K, Corey EJ. A short enantioselective total synthesis of the fundamental pentacyclic triterpene lupeol. Journal of the American Chemical Society. 131: 13928-9. PMID 19788328 DOI: 10.1021/Ja906335U |
0.397 |
|
| 2009 |
Kürti L, Blewett MM, Corey EJ. Origin of enantioselectivity in the Jacobsen epoxidation of olefins. Organic Letters. 11: 4592-5. PMID 19754126 DOI: 10.1021/Ol901859D |
0.754 |
|
| 2009 |
Shenvi RA, Corey EJ. A short and efficient synthesis of (-)-7-methylomuralide, a potent proteasome inhibitor. Journal of the American Chemical Society. 131: 5746-7. PMID 19338298 DOI: 10.1021/Ja901400Q |
0.774 |
|
| 2009 |
Chein RJ, Yeung YY, Corey EJ. Highly enantioselective oxazaborolidine-catalyzed reduction of 1,3-dicarbonyl compounds: role of the additive diethylaniline. Organic Letters. 11: 1611-4. PMID 19278241 DOI: 10.1021/Ol900258F |
0.61 |
|
| 2009 |
Corey EJ. Enantioselective catalysis based on cationic oxazaborolidines. Angewandte Chemie (International Ed. in English). 48: 2100-17. PMID 19235825 DOI: 10.1002/Anie.200805374 |
0.329 |
|
| 2009 |
Baqi Y, Giroux S, Corey EJ. A study of the epoxidation of cycloolefins by the t-BuOH copper-permanganate system. Organic Letters. 11: 959-61. PMID 19182889 DOI: 10.1021/Ol802923N |
0.758 |
|
| 2009 |
Corey E, Czakó B, Kürti L, Mammoto A, Ingber D. Synthesis of Cortistatin Analogues Synfacts. 2009: 1316-1316. DOI: 10.1055/S-0029-1218326 |
0.689 |
|
| 2009 |
Shenvi RA, Corey EJ. Synthesis of (-)-7-Methylomuralide Synfacts. 2009: 1193-1193. DOI: 10.1055/S-0029-1218031 |
0.794 |
|
| 2009 |
Corey E, Yeung Y. Synthesis of a Platensimycin Mimic Synfacts. 2009: 0243-0243. DOI: 10.1055/s-0028-1087695 |
0.31 |
|
| 2009 |
Zhdanov RI, Corey EJ. In memorium Igor Torgov: Torgov's way to total steroid synthesis Steroids. 74: 723-724. DOI: 10.1016/J.Steroids.2009.03.004 |
0.32 |
|
| 2008 |
Giroux S, Corey EJ. Enantioselective synthesis of a simple benzenoid analogue of glycinoeclepin A. Organic Letters. 10: 5617-9. PMID 19007174 DOI: 10.1021/Ol8024633 |
0.787 |
|
| 2008 |
Kürti L, Czakó B, Corey EJ. A short, scalable synthesis of the carbocyclic core of the anti-angiogenic cortistatins from (+)-estrone by B-ring expansion. Organic Letters. 10: 5247-50. PMID 18959422 DOI: 10.1021/Ol802328N |
0.673 |
|
| 2008 |
Yeung YY, Corey EJ. A simple, efficient, and enantiocontrolled synthesis of a near-structural mimic of platensimycin. Organic Letters. 10: 3877-8. PMID 18665602 DOI: 10.1021/Ol801400A |
0.615 |
|
| 2008 |
Giroux S, Bethke A, Fielenbach N, Antebi A, Corey EJ. Syntheses and biological evaluation of B-ring-modified analogues of dafachronic acid A. Organic Letters. 10: 3643-5. PMID 18642835 DOI: 10.1021/Ol801425V |
0.761 |
|
| 2008 |
Surendra K, Corey EJ. Rapid and enantioselective synthetic approaches to germanicol and other pentacyclic triterpenes. Journal of the American Chemical Society. 130: 8865-9. PMID 18597440 DOI: 10.1021/Ja802730A |
0.414 |
|
| 2008 |
Canales E, Corey EJ. Highly enantioselective [4 + 2] cycloaddition reactions catalyzed by a chiral N-methyl-oxazaborolidinium cation. Organic Letters. 10: 3271-3. PMID 18582066 DOI: 10.1021/Ol8011502 |
0.421 |
|
| 2008 |
Kürti L, Chein RJ, Corey EJ. Conformational energetics of cationic backbone rearrangements in triterpenoid biosynthesis provide an insight into enzymatic control of product. Journal of the American Chemical Society. 130: 9031-6. PMID 18558677 DOI: 10.1021/Ja800980H |
0.621 |
|
| 2008 |
Behenna DC, Corey EJ. Simple enantioselective approach to synthetic limonoids. Journal of the American Chemical Society. 130: 6720-1. PMID 18444655 DOI: 10.1021/Ja802376G |
0.792 |
|
| 2008 |
Hicken EJ, Corey EJ. Stereoselective synthesis of woody fragrances related to georgyone and arborone. Organic Letters. 10: 1135-8. PMID 18303897 DOI: 10.1021/Ol8000359 |
0.36 |
|
| 2008 |
Larionov OV, Corey EJ. An unconventional approach to the enantioselective synthesis of caryophylloids. Journal of the American Chemical Society. 130: 2954-5. PMID 18278923 DOI: 10.1021/Ja8003705 |
0.677 |
|
| 2008 |
Liau BB, Gnanadesikan V, Corey EJ. A study of the effect of Z- and E-olefinic geometry on the rates of ring closure of 13-membered dienes. Organic Letters. 10: 1055-7. PMID 18275205 DOI: 10.1021/Ol702868Z |
0.657 |
|
| 2008 |
Giroux S, Corey EJ. An efficient, stereocontrolled synthesis of the 25-(R)-diastereomer of dafachronic acid A from beta-ergosterol. Organic Letters. 10: 801-2. PMID 18247628 DOI: 10.1021/Ol702936F |
0.746 |
|
| 2008 |
Lalic G, Corey EJ. Enantioselective rhodium(I)-triethylamine catalyzed addition of potassium isopropenyl trifluoroborate to enones Tetrahedron Letters. 49: 4894-4896. DOI: 10.1016/J.Tetlet.2008.05.147 |
0.683 |
|
| 2007 |
Lalic G, Corey EJ. An effective enantioselective route to the platensimycin core. Organic Letters. 9: 4921-3. PMID 17929829 DOI: 10.1021/Ol702323S |
0.665 |
|
| 2007 |
Canales E, Corey EJ. Highly enantioselective [2+2]-cycloaddition reactions catalyzed by a chiral aluminum bromide complex. Journal of the American Chemical Society. 129: 12686-7. PMID 17900126 DOI: 10.1021/Ja0765262 |
0.432 |
|
| 2007 |
Yeung YY, Chein RJ, Corey EJ. Conversion of Torgov's synthesis of estrone into a highly enantioselective and efficient process. Journal of the American Chemical Society. 129: 10346-7. PMID 17672468 DOI: 10.1021/Ja0742434 |
0.617 |
|
| 2007 |
Giroux S, Corey EJ. Stereocontrolled synthesis of dafachronic acid A, the ligand for the DAF-12 nuclear receptor of Caenorhabditis elegans. Journal of the American Chemical Society. 129: 9866-7. PMID 17658816 DOI: 10.1021/Ja074306I |
0.761 |
|
| 2007 |
Shen R, Corey EJ. Studies of the stereochemistry of [2+2]-photocycloaddition reactions of 2-cyclohexenones with olefins. Organic Letters. 9: 1057-9. PMID 17291002 DOI: 10.1021/Ol063092R |
0.303 |
|
| 2007 |
Liu D, Canales E, Corey EJ. Chiral oxazaborolidine-aluminum bromide complexes are unusually powerful and effective catalysts for enantioselective Diels-Alder reactions. Journal of the American Chemical Society. 129: 1498-9. PMID 17283985 DOI: 10.1021/Ja068637R |
0.357 |
|
| 2007 |
Yeung YY, Corey EJ. An efficient process for the bromolactamization of unsaturated acids Tetrahedron Letters. 48: 7567-7570. DOI: 10.1016/J.Tetlet.2007.08.113 |
0.32 |
|
| 2007 |
Ryu DH, Kim KH, Sim JY, Corey EJ. Catalytic enantioselective Diels-Alder reactions of furans and 1,1,1-trifluoroethyl acrylate Tetrahedron Letters. 48: 5735-5737. DOI: 10.1016/J.Tetlet.2007.06.097 |
0.349 |
|
| 2006 |
Mushti CS, Kim JH, Corey EJ. Total synthesis of antheliolide A. Journal of the American Chemical Society. 128: 14050-2. PMID 17061886 DOI: 10.1055/S-2007-968201 |
0.404 |
|
| 2006 |
Gnanadesikan V, Corey EJ. Enantioselective beta-lactone formation from ketene and aldehydes catalyzed by a chiral oxazaborolidine. Organic Letters. 8: 4943-5. PMID 17020342 DOI: 10.1021/Ol061979H |
0.362 |
|
| 2006 |
Yeung YY, Gao X, Corey EJ. A general process for the haloamidation of olefins. Scope and mechanism. Journal of the American Chemical Society. 128: 9644-5. PMID 16866514 DOI: 10.1021/Ja063675W |
0.629 |
|
| 2006 |
Reddy BV, Reddy LR, Corey EJ. Novel acetoxylation and C-C coupling reactions at unactivated positions in alpha-amino acid derivatives. Organic Letters. 8: 3391-4. PMID 16836413 DOI: 10.1021/Ol061389J |
0.331 |
|
| 2006 |
Rege PD, Tian Y, Corey EJ. Studies of new indole alkaloid coupling methods for the synthesis of haplophytine. Organic Letters. 8: 3117-20. PMID 16805566 DOI: 10.1021/Ol061319C |
0.411 |
|
| 2006 |
Liu D, Hong S, Corey EJ. Enantioselective synthesis of bridged- or fused-ring bicyclic ketones by a catalytic asymmetric Michael addition pathway. Journal of the American Chemical Society. 128: 8160-1. PMID 16787080 DOI: 10.1021/Ja063332Y |
0.611 |
|
| 2006 |
Reddy LR, Reddy BV, Corey EJ. Efficient method for selective introduction of substituents as C5 of isoleucine and other alpha-amino acids. Organic Letters. 8: 2819-21. PMID 16774265 DOI: 10.1021/Ol060952V |
0.364 |
|
| 2006 |
Yeung YY, Hong S, Corey EJ. A short enantioselective pathway for the synthesis of the anti-influenza neuramidase inhibitor oseltamivir from 1,3-butadiene and acrylic acid. Journal of the American Chemical Society. 128: 6310-1. PMID 16683783 DOI: 10.1021/Ja0616433 |
0.724 |
|
| 2006 |
Reddy LR, Corey EJ. Novel bicyclization reaction leading to a fused beta-lactone. Organic Letters. 8: 1717-9. PMID 16597149 DOI: 10.1021/Ol060464N |
0.31 |
|
| 2006 |
Mascitti V, Corey EJ. Enantioselective synthesis of pentacycloanammoxic acid. Journal of the American Chemical Society. 128: 3118-9. PMID 16522072 DOI: 10.1021/Ja058370G |
0.379 |
|
| 2006 |
Hong S, Corey EJ. Enantioselective syntheses of georgyone, arborone, and structural relatives. Relevance to the molecular-level understanding of olfaction. Journal of the American Chemical Society. 128: 1346-52. PMID 16433554 DOI: 10.1021/Ja057483X |
0.511 |
|
| 2006 |
Snyder SA, Corey EJ. Concise total syntheses of palominol, dolabellatrienone, beta-araneosene, and isoedunol via an enantioselective Diels-Alder macrobicyclization. Journal of the American Chemical Society. 128: 740-2. PMID 16417362 DOI: 10.1021/Ja0576379 |
0.687 |
|
| 2006 |
Weatherhead-Kloster RA, Corey EJ. Theory-guided discovery of unique chemical transformations of cyclopropenes. Organic Letters. 8: 171-4. PMID 16381595 DOI: 10.1021/Ol052752+ |
0.335 |
|
| 2006 |
Corey E, Mascitti V. Synthesis of Pentacycloanammoxic Acid Synfacts. 2006: 0759-0759. DOI: 10.1055/S-2006-941927 |
0.38 |
|
| 2006 |
Corey E, Snyder S. Synthesis of Palominol and Dolabellatrienone Synfacts. 2006: 0531-0531. DOI: 10.1055/S-2006-934485 |
0.697 |
|
| 2006 |
Kingsbury JS, Corey EJ. Synthesis of Isoedunol and β-Araneosene Synfacts. 2006: 185-185. DOI: 10.1055/S-2006-931924 |
0.308 |
|
| 2006 |
Zhou G, Corey EJ. Synthesis of Aflatoxin B2 Synfacts. 2006: 105-105. DOI: 10.1055/S-2005-921774 |
0.334 |
|
| 2006 |
Mascitti V, Corey EJ. Photochemical studies on ladderane formation from conjugated esters in solution or solid phase Tetrahedron Letters. 47: 5879-5882. DOI: 10.1016/J.Tetlet.2006.06.066 |
0.31 |
|
| 2006 |
Hong BC, Kim S, Kim TS, Corey EJ. Synthesis and properties of several isomers of the cardioactive steroid ouabain Tetrahedron Letters. 47: 2711-2715. DOI: 10.1016/J.Tetlet.2006.02.089 |
0.654 |
|
| 2006 |
Mi Y, Corey EJ. A practical synthesis of S-quinuclidine-2-carboxylic acid and its enantiomer Tetrahedron Letters. 47: 2515-2516. DOI: 10.1016/J.Tetlet.2006.02.064 |
0.366 |
|
| 2006 |
Chau FHV, Corey EJ. Short and simple synthesis of chelating bis-ethers and bis-amines in the bicyclo[3.3.1]nonane series Tetrahedron Letters. 47: 2581-2583. DOI: 10.1016/J.Tetlet.2006.02.038 |
0.421 |
|
| 2006 |
Ge M, Corey EJ. A method for the catalytic enantioselective synthesis of 6-silylated 2-cyclohexenones Tetrahedron Letters. 47: 2319-2321. DOI: 10.1016/J.Tetlet.2006.02.014 |
0.378 |
|
| 2006 |
Snyder SA, Corey EJ. Regioselective aldol condensations of a cholestanone-derived dialdehyde: New twists on a classic reaction Tetrahedron Letters. 47: 2083-2086. DOI: 10.1016/J.Tetlet.2006.01.136 |
0.673 |
|
| 2005 |
Hogan PC, Corey EJ. Proteasome inhibition by a totally synthetic beta-lactam related to salinosporamide A and omuralide. Journal of the American Chemical Society. 127: 15386-7. PMID 16262399 DOI: 10.1021/Ja056284A |
0.663 |
|
| 2005 |
Lou Y, Remarchuk TP, Corey EJ. Catalysis of enantioselective [2+1]-cycloaddition reactions of ethyl diazoacetate and terminal acetylenes using mixed-ligand complexes of the series Rh2(RCO2)n(L*4-n). Stereochemical heuristics for ligand exchange and catalyst synthesis. Journal of the American Chemical Society. 127: 14223-30. PMID 16218616 DOI: 10.1021/Ja052254W |
0.353 |
|
| 2005 |
Kingsbury JS, Corey EJ. Enantioselective total synthesis of isoedunol and beta-araneosene featuring unconventional strategy and methodology. Journal of the American Chemical Society. 127: 13813-5. PMID 16201801 DOI: 10.1021/Ja055137+ |
0.4 |
|
| 2005 |
Zhou G, Corey EJ. Short, enantioselective total synthesis of aflatoxin B2 using an asymmetric [3+2]-cycloaddition step. Journal of the American Chemical Society. 127: 11958-9. PMID 16117532 DOI: 10.1021/Ja054503M |
0.408 |
|
| 2005 |
Reddy LR, Fournier JF, Subba Reddy BV, Corey EJ. An efficient, stereocontrolled synthesis of a potent omuralide-salinosporin hybrid for selective proteasome inhibition. Journal of the American Chemical Society. 127: 8974-6. PMID 15969573 DOI: 10.1021/Ja052376O |
0.627 |
|
| 2005 |
Reddy LR, Saravanan P, Fournier JF, Subba Reddy BV, Corey EJ. Simple enantiospecific syntheses of the C(2)-diastereomers of omuralide and 3-methylomuralide. Organic Letters. 7: 2703-5. PMID 15957926 DOI: 10.1021/Ol050874W |
0.621 |
|
| 2005 |
Reddy LR, Fournier JF, Reddy BV, Corey EJ. New synthetic route for the enantioselective total synthesis of salinosporamide A and biologically active analogues. Organic Letters. 7: 2699-701. PMID 15957925 DOI: 10.1021/Ol0508734 |
0.656 |
|
| 2005 |
Ryu DH, Corey EJ. Enantioselective cyanosilylation of ketones catalyzed by a chiral oxazaborolidinium ion. Journal of the American Chemical Society. 127: 5384-7. PMID 15826176 DOI: 10.1021/Ja050543E |
0.657 |
|
| 2005 |
Ryu DH, Zhou G, Corey EJ. Nonparallelism between reaction rate and dienophile-catalyst affinity in catalytic enantioselective Diels-Alder reactions. Organic Letters. 7: 1633-6. PMID 15816770 DOI: 10.1021/Ol0503236 |
0.612 |
|
| 2005 |
Yu JQ, Wu HC, Corey EJ. Pd(OH)2/C-mediated selective oxidation of silyl enol ethers by tert-butylhydroperoxide, a useful method for the conversion of ketones to alpha,beta-enones or beta-silyloxy-alpha,beta-enones. Organic Letters. 7: 1415-7. PMID 15787520 DOI: 10.1021/Ol050284Y |
0.48 |
|
| 2005 |
Reddy BVS, Reddy LR, Corey EJ. Dimethylaluminum methyltellurate, a new reagent for the cleavage of hindered methyl esters under exceptionally mild conditions by a novel mechanism Tetrahedron Letters. 46: 4589-4593. DOI: 10.1016/J.Tetlet.2005.05.003 |
0.333 |
|
| 2004 |
Mascitti V, Corey EJ. Total synthesis of (+/-)-pentacycloanammoxic acid. Journal of the American Chemical Society. 126: 15664-5. PMID 15571387 DOI: 10.1021/Ja044089A |
0.386 |
|
| 2004 |
Hu QY, Zhou G, Corey EJ. Application of chiral cationic catalysts to several classical syntheses of racemic natural products transforms them into highly enantioselective pathways. Journal of the American Chemical Society. 126: 13708-13. PMID 15493929 DOI: 10.1021/Ja046154M |
0.406 |
|
| 2004 |
Zhang FY, Corey EJ. Highly enantioselective dimerization of alpha,beta-enones catalyzed by a rigid quaternary ammonium salt. Organic Letters. 6: 3397-9. PMID 15355061 DOI: 10.1021/Ol048583V |
0.339 |
|
| 2004 |
Kwak YS, Corey EJ. Catalytic enantioselective conjugate addition of trimethylsilylacetylene to 2-cyclohexen-1-one. Organic Letters. 6: 3385-8. PMID 15355058 DOI: 10.1021/Ol048623V |
0.343 |
|
| 2004 |
Lou Y, Horikawa M, Kloster RA, Hawryluk NA, Corey EJ. A new chiral Rh(II) catalyst for enantioselective [2 + 1]-cycloaddition. mechanistic implications and applications. Journal of the American Chemical Society. 126: 8916-8. PMID 15264821 DOI: 10.1021/Ja047064K |
0.796 |
|
| 2004 |
Ryu DH, Corey EJ. Highly enantioselective cyanosilylation of aldehydes catalyzed by a chiral oxazaborolidinium ion. Journal of the American Chemical Society. 126: 8106-7. PMID 15225038 DOI: 10.1002/chin.200444038 |
0.619 |
|
| 2004 |
Hu QY, Rege PD, Corey EJ. Simple, catalytic enantioselective syntheses of estrone and desogestrel. Journal of the American Chemical Society. 126: 5984-6. PMID 15137761 DOI: 10.1021/Ja048808X |
0.373 |
|
| 2004 |
Ryu DH, Zhou G, Corey EJ. Enantioselective and structure-selective Diels-Alder reactions of unsymmetrical quinones catalyzed by a chiral oxazaborolidinium cation. Predictive selection rules. Journal of the American Chemical Society. 126: 4800-2. PMID 15080683 DOI: 10.1021/Ja049323B |
0.632 |
|
| 2003 |
Davidson JP, Corey EJ. First enantiospecific total synthesis of the antitubercular marine natural product pseudopteroxazole. Revision of assigned stereochemistry. Journal of the American Chemical Society. 125: 13486-9. PMID 14583045 DOI: 10.1021/Ja0378916 |
0.415 |
|
| 2003 |
Zhou G, Hu QY, Corey EJ. Useful enantioselective bicyclization reactions using an N-protonated chiral oxazaborolidine as catalyst. Organic Letters. 5: 3979-82. PMID 14535758 DOI: 10.1021/Ol035542A |
0.357 |
|
| 2003 |
Huang J, Corey EJ. A mechanistically guided design leads to the synthesis of an efficient and practical new reagent for the highly enantioselective, catalytic dihydroxylation of olefins. Organic Letters. 5: 3455-8. PMID 12967298 DOI: 10.1021/Ol035192S |
0.361 |
|
| 2003 |
Sprott KT, Corey EJ. A new cationic, chiral catalyst for highly enantioselective Diels-Alder reactions. Organic Letters. 5: 2465-7. PMID 12841756 DOI: 10.1021/Ol034706K |
0.377 |
|
| 2003 |
Ryu DH, Corey EJ. Triflimide activation of a chiral oxazaborolidine leads to a more general catalytic system for enantioselective Diels-Alder addition. Journal of the American Chemical Society. 125: 6388-90. PMID 12785777 DOI: 10.1021/Ja035393R |
0.657 |
|
| 2003 |
Baran PS, Guerrero CA, Corey EJ. The first method for protection-deprotection of the indole 2,3-pi bond. Organic Letters. 5: 1999-2001. PMID 12762706 DOI: 10.1021/Ol034634X |
0.779 |
|
| 2003 |
Baran PS, Guerrero CA, Corey EJ. Short, enantioselective total synthesis of okaramine N. Journal of the American Chemical Society. 125: 5628-9. PMID 12733890 DOI: 10.1021/Ja034491+ |
0.792 |
|
| 2003 |
Yu JQ, Corey EJ. A mild, catalytic, and highly selective method for the oxidation of alpha,beta-enones to 1,4-enediones. Journal of the American Chemical Society. 125: 3232-3. PMID 12630876 DOI: 10.1021/Ja0340735 |
0.496 |
|
| 2003 |
Corey EJ, Noe MC. Preparation of O‐Allyl‐N‐(9‐Anthracenylmethyl)cinchonidinium Bromide as a Phase Transfer Catalyst for the Enantioselective Alkylation of Glycine Benzophenone Imine tert‐Butyl Ester: (4S)‐2‐(Benzhydrylidenamino)pentanedioic Acid, 1‐tert‐Butyl Ester‐5‐Methyl Ester Organic Syntheses. 80: 38-45. DOI: 10.1002/0471264180.Os080.05 |
0.353 |
|
| 2003 |
Pikul S, Corey EJ. Enantioselective, Catalytic Diels‐Alder Reaction: (1S‐endo)‐3‐(Bicyclo[2.2.1]Hept‐5‐en‐2‐ylcarbonyl)‐2‐Oxazolidinone Organic Syntheses. 30-30. DOI: 10.1002/0471264180.Os071.04 |
0.342 |
|
| 2003 |
Corey EJ, Seebach D. 1,3-Dithiane Organic Syntheses. 72-72. DOI: 10.1002/0471264180.Os050.22 |
0.53 |
|
| 2002 |
Corey EJ. Catalytic enantioselective Diels--Alder reactions: methods, mechanistic fundamentals, pathways, and applications. Angewandte Chemie (International Ed. in English). 41: 1650-67. PMID 19750685 DOI: 10.1002/1521-3773(20020517)41:10<1650::Aid-Anie1650>3.0.Co;2-B |
0.362 |
|
| 2002 |
Radetich B, Corey EJ. A study of oligoprenyl coupling reactions with allylic stannanes. Organic Letters. 4: 3463-4. PMID 12323044 DOI: 10.1021/Ol026568P |
0.301 |
|
| 2002 |
Mi Y, Schreiber JV, Corey EJ. Total synthesis of (+)-alpha-onocerin in four steps via four-component coupling and tetracyclization steps. Journal of the American Chemical Society. 124: 11290-1. PMID 12236742 DOI: 10.1021/Ja027373F |
0.441 |
|
| 2002 |
Ryu DH, Lee TW, Corey EJ. Broad-spectrum enantioselective diels-alder catalysis by chiral, cationic oxazaborolidines. Journal of the American Chemical Society. 124: 9992-3. PMID 12188655 DOI: 10.1021/Ja027468H |
0.68 |
|
| 2002 |
Yu JQ, Corey EJ. Diverse pathways for the palladium(II)-mediated oxidation of olefins by tert-butylhydroperoxide. Organic Letters. 4: 2727-30. PMID 12153220 DOI: 10.1021/Ol0262340 |
0.519 |
|
| 2002 |
Hu T, Corey EJ. Short syntheses of (+/-)-delta-araneosene and humulene utilizing a combination of four-component assembly and palladium-mediated cyclization. Organic Letters. 4: 2441-3. PMID 12098267 DOI: 10.1021/Ol026205P |
0.305 |
|
| 2002 |
Baran PS, Corey EJ. A short synthetic route to (+)-austamide, (+)-deoxyisoaustamide, and (+)-hydratoaustamide from a common precursor by a novel palladium-mediated indole --> dihydroindoloazocine cyclization. Journal of the American Chemical Society. 124: 7904-5. PMID 12095326 DOI: 10.1021/Ja026663T |
0.669 |
|
| 2002 |
Corey EJ, Shibata T, Lee TW. Asymmetric Diels-Alder reactions catalyzed by a triflic acid activated chiral oxazaborolidine. Journal of the American Chemical Society. 124: 3808-9. PMID 11942799 DOI: 10.1021/Ja025848X |
0.541 |
|
| 2002 |
Radetich B, Corey EJ. A general stereocontrolled, convergent synthesis of oligoprenols that parallels the biosynthetic pathway. Journal of the American Chemical Society. 124: 2430-1. PMID 11890779 DOI: 10.1021/Ja0127537 |
0.366 |
|
| 2002 |
Corey EJ, Weigel LO, Floyd D, Bock MG. Total synthesis of (.+-.)-N-methylmaysenine Cheminform. 11. DOI: 10.1021/Ja00524A046 |
0.326 |
|
| 2002 |
Corey EJ, Hua DH, Pan BC, Seitz SP. Total Synthesis Of Aplasmomycin Cheminform. 14. DOI: 10.1002/Chin.198309340 |
0.418 |
|
| 2002 |
Corey EJ, Niwa H, Knolle J. Total synthesis of (S)-12-hydroxy-5,8,14-cis,-10-trans-eicosatetraenoic acid (Samuelsson's HETE) Cheminform. 9. DOI: 10.1002/Chin.197827145 |
0.331 |
|
| 2002 |
Corey EJ, Beames DJ. A Method For The Protection Of Lactones And Esters Against Nucleophilic Attack Cheminform. 4. DOI: 10.1002/Chin.197344213 |
0.3 |
|
| 2002 |
Corey EJ, Nicolaou KC, Snyder SA, Montagnon T, Vassilikogiannakis G. Cover Picture: Angew. Chem. Int. Ed. 10/2002 Angewandte Chemie International Edition. 41: 1629-1629. DOI: 10.1002/1521-3773(20020517)41:10<1629::Aid-Anie1629>3.0.Co;2-0 |
0.709 |
|
| 2002 |
Corey EJ, Nicolaou KC, Snyder SA, Montagnon T, Vassilikogiannakis GE. Titelbild: Angew. Chem. 10/2002 Angewandte Chemie. 114: 1703-1703. DOI: 10.1002/1521-3757(20020517)114:10<1703::Aid-Ange1703>3.0.Co;2-# |
0.674 |
|
| 2001 |
Arrow KJ, Axelrod J, Benacerraf B, Berg P, Bishop JM, Bloembergen N, Brown HC, Cibelli J, Cohen S, Cooper LN, Corey EJ, Cronin JW, Curl R, Dulbecco R, Fischer EH, et al. Nobel laureates' letter to President Bush. The Washington Post. A02. PMID 12462241 |
0.465 |
|
| 2001 |
Hu T, Corey EJ. A novel and selective photoisomerization of allylic benzoates. Organic Letters. 3: 3547-8. PMID 11678704 DOI: 10.1021/Ol016657M |
0.323 |
|
| 2001 |
Lee TW, Corey EJ. (2-methoxyphenyl)dimethylsilyl lithium and cuprate reagents offer unique advantages in multistep synthesis. Organic Letters. 3: 3337-9. PMID 11594828 DOI: 10.1021/Ol0165746 |
0.485 |
|
| 2001 |
Zhang J, Corey EJ. A simple enantioselective synthesis of serratenediol. Organic Letters. 3: 3215-6. PMID 11574034 DOI: 10.1021/Ol016543A |
0.44 |
|
| 2001 |
Corey EJ, Zhang J. Highly effective transition structure designed catalyst for the enantio- and position-selective dihydroxylation of polyisoprenoids. Organic Letters. 3: 3211-4. PMID 11574033 DOI: 10.1021/Ol016577I |
0.338 |
|
| 2001 |
Johnson TW, Corey EJ. Enantiospecific synthesis of the proposed structure of the antitubercular marine diterpenoid pseudopteroxazole: revision of stereochemistry. Journal of the American Chemical Society. 123: 4475-9. PMID 11457233 DOI: 10.1021/Ja010221K |
0.395 |
|
| 2001 |
Lee TW, Corey EJ. Enantioselective total synthesis of eunicenone A. Journal of the American Chemical Society. 123: 1872-7. PMID 11456807 DOI: 10.1021/Ja004043R |
0.6 |
|
| 2001 |
Crane SN, Corey EJ. A novel enantioselective synthetic route to omuralide analogues with the potential for species selectivity in proteasome inhibition. Organic Letters. 3: 1395-7. PMID 11348243 DOI: 10.1021/Ol015757P |
0.382 |
|
| 2001 |
Zhang F, Corey EJ. Enantio- and diastereoselective michael reactions of silyl enol ethers and chalcones by catalysis using a chiral quaternary ammonium salt. Organic Letters. 3: 639-41. PMID 11178845 DOI: 10.1021/Ol015592K |
0.37 |
|
| 2001 |
Corey EJ, Lee TW. The formyl C–H⋯O hydrogen bond as a critical factor in enantioselective Lewis-acid catalyzed reactions of aldehydes Chemical Communications. 1321-1329. DOI: 10.1039/B104800G |
0.337 |
|
| 2001 |
Breuning M, Corey EJ. Catalytic Enantioselective Diels-Alder Reactions of 1,4-Quinone Monoketals Organic Letters. 3: 1559-1562. DOI: 10.1021/Ol015852Y |
0.37 |
|
| 2001 |
Corey EJ, Lee TW. The formyl C-H···O hydrogen bond as a critical factor in enantioselective Lewis-acid catalyzed reactions of aldehydes Chemical Communications. 1321-1329. |
0.437 |
|
| 2000 |
Corey EJ, Zhang FY. Enantioselective Michael addition of nitromethane to alpha, beta-enones catalyzed by chiral quaternary ammonium salts. A simple synthesis of (R)-baclofen. Organic Letters. 2: 4257-9. PMID 11150213 DOI: 10.1021/Ol0068344 |
0.353 |
|
| 2000 |
Han X, Crane SN, Corey EJ. A short catalytic enantioselective synthesis of the vascular antiinflammatory eicosanoid (11R,12S)-oxidoarachidonic acid. Organic Letters. 2: 3437-8. PMID 11082002 DOI: 10.1021/Ol006430B |
0.38 |
|
| 2000 |
Wendt KU, Schulz GE, Corey EJ, Liu DR. Enzyme Mechanisms for Polycyclic Triterpene Formation. Angewandte Chemie (International Ed. in English). 39: 2812-2833. PMID 11027983 DOI: 10.1002/1521-3773(20000818)39:16<2812::Aid-Anie2812>3.0.Co;2-# |
0.457 |
|
| 2000 |
Wendt KU, Schulz GE, Corey EJ, Liu DR. Cover Picture. Angewandte Chemie (International Ed. in English). 39: 2795. PMID 11027982 DOI: 10.1002/1521-3773(20000818)39:16<2795::AID-ANIE2795>3.0.CO;2-8 |
0.382 |
|
| 2000 |
Han X, Corey EJ. A short catalytic enantioselective synthesis of the proinflammatory eicosanoid 12(R)-hydroxy- 5(Z),8(Z),10(E),14(Z)-eicosatetraenoic acid (12(R)-HETE). Organic Letters. 2: 2543-4. PMID 10956542 DOI: 10.1021/Ol0062392 |
0.332 |
|
| 2000 |
Lazerwith SE, Johnson TW, Corey EJ. Syntheses and stereochemical revision of pseudopterosin G-J aglycon and helioporin E. Organic Letters. 2: 2389-92. PMID 10930291 DOI: 10.1021/Ol006192K |
0.715 |
|
| 2000 |
Ge M, Stoltz BM, Corey EJ. Mechanistic Insights into the Factors Determining Exo-Endo Selectivity in the Lewis Acid-Catalyzed Diels-Alder Reaction of 1,3-Dienes with 2-Cycloalkenones. Organic Letters. 2: 1927-1929. PMID 10891193 DOI: 10.1021/Ol0060026 |
0.646 |
|
| 2000 |
Busch-Petersen J, Corey EJ. A Rhodium(II) catalytic approach to the synthesis of ethers of a minor component in a tautomeric set. Organic Letters. 2: 1641-3. PMID 10841499 DOI: 10.1021/Ol005964+ |
0.392 |
|
| 2000 |
Zhang FY, Corey EJ. Highly enantioselective Michael reactions catalyzed by a chiral quaternary ammonium salt. Illustration by asymmetric syntheses of (S)-ornithine and chiral 2-cyclohexenones. Organic Letters. 2: 1097-100. PMID 10804563 DOI: 10.1021/Ol0056527 |
0.385 |
|
| 2000 |
Martinez EJ, Corey EJ. A new, more efficient, and effective process for the synthesis of a key pentacyclic intermediate for production of ecteinascidin and phthalascidin antitumor agents. Organic Letters. 2: 993-6. PMID 10768205 DOI: 10.1021/Ol0056729 |
0.388 |
|
| 2000 |
Xiong Z, Corey EJ. Simple enantioselective total synthesis of glabrescol, a chiral C2-symmetric pentacyclic oxasqualenoid [17] Journal of the American Chemical Society. 122: 9328-9329. DOI: 10.1021/Ja0024901 |
0.405 |
|
| 2000 |
Stoltz BM, Kano T, Corey EJ. Enantioselective total synthesis of nicandrenones [10] Journal of the American Chemical Society. 122: 9044-9045. DOI: 10.1021/Ja0024892 |
0.659 |
|
| 2000 |
Xiong Z, Corey EJ. Simple total synthesis of the pentacyclic C(s)-symmetric structure attributed to the squalenoid glabrescol and three C(s)-symmetric diastereomers compel structural revision Journal of the American Chemical Society. 122: 4831-4832. DOI: 10.1021/Ja000842Y |
0.308 |
|
| 2000 |
Busch-Petersen J, Corey EJ. Lithium N-trityl-N-(R)-1-phenethylamide, a readily available and useful base for the enantioselective formation of chiral enolates from achiral ketones Tetrahedron Letters. 41: 6941-6944. DOI: 10.1016/S0040-4039(00)01185-0 |
0.318 |
|
| 2000 |
Corey EJ, Choi S. Chiral diazaborolidine-mediated enantioselective aldol reactions of phenylthioacetate esters Tetrahedron Letters. 41: 2769-2772. DOI: 10.1016/S0040-4039(00)00302-6 |
0.392 |
|
| 2000 |
Wendt K, Schulz G, Corey E, Liu D. Mechanismen der enzymatischen Bildung polycyclischer Triterpene Angewandte Chemie. 112: 2930-2952. DOI: 10.1002/1521-3757(20000818)112:16<2930::Aid-Ange2930>3.0.Co;2-S |
0.393 |
|
| 1999 |
Han X, Corey EJ. A catalytic enantioselective total synthesis of (-)-wodeshiol. Organic Letters. 1: 1871-2. PMID 10836046 DOI: 10.1021/Ol991151D |
0.378 |
|
| 1999 |
Sarakinos G, Corey EJ. A practical new chiral controller for asymmetric Diels-Alder and alkylation reactions. Organic Letters. 1: 1741-4. PMID 10836034 DOI: 10.1021/Ol991007S |
0.376 |
|
| 1999 |
Barnes-Seeman D, Corey EJ. A two-step total synthesis of the natural pentacycle trichodimerol, a novel inhibitor of TNF-alpha production. Organic Letters. 1: 1503-4. PMID 10825998 DOI: 10.1021/Ol991070H |
0.794 |
|
| 1999 |
Steinhagen H, Corey EJ. A simple convergent approach to the synthesis of the antiviral agent virantmycin. Organic Letters. 1: 823-4. PMID 10823211 DOI: 10.1021/Ol9908575 |
0.318 |
|
| 1999 |
Sarakinos G, Corey EJ. Simple and practical routes to enantiomerically pure 5-(trialkylsilyl)-2-cyclohexenones. Organic Letters. 1: 811-4. PMID 10823209 DOI: 10.1021/Ol990805F |
0.395 |
|
| 1999 |
Martinez EJ, Corey EJ. Enantioselective synthesis of saframycin A and evaluation of antitumor activity relative to ecteinascidin/saframycin hybrids. Organic Letters. 1: 75-7. PMID 10822537 DOI: 10.1021/Ol990553I |
0.41 |
|
| 1999 |
Lanza RP, Arrow KJ, Axelrod J, Baltimore D, Benacerraf B, Bloch KE, Bloembergen N, Brown HC, Brown MS, Cibelli JB, Cohen S, Cooper LN, Corey EJ, Dulbecco R, Fischer EH, et al. Science over politics. Science (New York, N.Y.). 283: 1849-50. PMID 10206888 DOI: 10.1126/Science.283.5409.1849B |
0.331 |
|
| 1999 |
Martinez EJ, Owa T, Schreiber SL, Corey EJ. Phthalascidin, a synthetic antitumor agent with potency and mode of action comparable to ecteinascidin 743. Proceedings of the National Academy of Sciences of the United States of America. 96: 3496-501. PMID 10097064 DOI: 10.1073/Pnas.96.7.3496 |
0.413 |
|
| 1999 |
Corey EJ, Li WD. Total synthesis and biological activity of lactacystin, omuralide and analogs. Chemical & Pharmaceutical Bulletin. 47: 1-10. PMID 9987821 DOI: 10.1248/Cpb.47.1 |
0.334 |
|
| 1999 |
Huang AX, Xiong Z, Corey EJ. An exceptionally short and simple enantioselective total synthesis of pentacyclic triterpenes of the β-amyrin family Journal of the American Chemical Society. 121: 9999-10003. DOI: 10.1021/Ja992411P |
0.366 |
|
| 1999 |
He F, Bo Y, Altom JD, Corey EJ. Enantioselective total synthesis of aspidophytine [13] Journal of the American Chemical Society. 121: 6771-6772. DOI: 10.1021/Ja9915201 |
0.633 |
|
| 1999 |
Han X, Stoltz BM, Corey EJ. Cuprous chloride accelerated Stille reactions. A general and effective coupling system for sterically congested substrates and for enantioselective synthesis Journal of the American Chemical Society. 121: 7600-7605. DOI: 10.1021/Ja991500Z |
0.649 |
|
| 1999 |
Corey EJ, Huang AX. A short enantioselective total synthesis of the third-generation oral contraceptive desogestrel Journal of the American Chemical Society. 121: 710-714. DOI: 10.1021/Ja983179A |
0.391 |
|
| 1999 |
Edelson BS, Stoltz BM, Corey EJ. A simple and effective procedure for removal of tri-n-butyltin halides from reaction mixtures Tetrahedron Letters. 40: 6729-6730. DOI: 10.1016/S0040-4039(99)01394-5 |
0.601 |
|
| 1999 |
Horikawa M, Busch-Petersen J, Corey EJ. Enantioselective synthesis of β-hydroxy-α-amino acid esters by aldol coupling using a chiral quaternary ammonium salt as catalyst Tetrahedron Letters. 40: 3843-3846. DOI: 10.1016/S0040-4039(99)00636-X |
0.388 |
|
| 1999 |
Busch-Petersen J, Bo Y, Corey EJ. New, practical and effective sources of fluoride ion for desilylation to form carbon anions Tetrahedron Letters. 40: 2065-2068. DOI: 10.1016/S0040-4039(99)00166-5 |
0.526 |
|
| 1999 |
Corey EJ, Stoltz BM. Novel annulation products derived by selective attack on the C(18) angular methyl group of the cardenolide ouabain Tetrahedron Letters. 40: 2061-2064. DOI: 10.1016/S0040-4039(99)00165-3 |
0.644 |
|
| 1999 |
Corey EJ, Li WDZ, Nagamitsu T, Fenteany G. The structural requirements for inhibition of proteasome function by the lactacystin-derived β-lactone and synthetic analogs Tetrahedron. 55: 3305-3316. DOI: 10.1016/S0040-4020(98)01142-9 |
0.707 |
|
| 1999 |
Corey EJ, Zhang FY. re- and si-face-selective nitroaldol reactions catalyzed by a rigid chiral quaternary ammonium salt: A highly stereoselective synthesis of the HIV protease inhibitor amprenavir (Vertex 478) Angewandte Chemie - International Edition. 38: 1931-1934. DOI: 10.1002/(Sici)1521-3773(19990712)38:13/14<1931::Aid-Anie1931>3.0.Co;2-4 |
0.362 |
|
| 1998 |
Corey EJ, Li W, Nagamitsu T. An Efficient and Concise Enantioselective Total Synthesis of Lactacystin. Angewandte Chemie (International Ed. in English). 37: 1676-1679. PMID 29711503 DOI: 10.1002/(Sici)1521-3773(19980703)37:12<1676::Aid-Anie1676>3.0.Co;2-T |
0.518 |
|
| 1998 |
Corey EJ, Guzman-Perez A. The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters. Angewandte Chemie (International Ed. in English). 37: 388-401. PMID 29711174 DOI: 10.1002/(Sici)1521-3773(19980302)37:4<388::Aid-Anie388>3.0.Co;2-V |
0.351 |
|
| 1998 |
Corey EJ, Helal CJ. Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method. Angewandte Chemie (International Ed. in English). 37: 1986-2012. PMID 29711061 DOI: 10.1002/(Sici)1521-3773(19980817)37:15<1986::Aid-Anie1986>3.0.Co;2-Z |
0.327 |
|
| 1998 |
Corey EJ, Luo G, Lin LS. Exceptionally Simple Enantioselective Syntheses of Chiral Hexa- and Tetracyclic Polyprenoids of Sedimentary Origin. Angewandte Chemie (International Ed. in English). 37: 1126-1128. PMID 29711018 DOI: 10.1002/(Sici)1521-3773(19980504)37:8<1126::Aid-Anie1126>3.0.Co;2-0 |
0.367 |
|
| 1998 |
Corey EJ, Lazerwith SE. A direct and efficient stereocontrolled synthetic route to the pseudopterosins, potent marine antiinflammatory agents Journal of the American Chemical Society. 120: 12777-12782. DOI: 10.1021/ja983041s |
0.725 |
|
| 1998 |
Corey EJ, Staas DD. Demonstration of a Common Concerted Mechanistic Pathway for the Acid-Catalyzed Cyclization of 5,6-Unsaturated Oxiranes in Chemical and Enzymatic Systems Journal of the American Chemical Society. 120: 3526-3527. DOI: 10.1021/Ja980096L |
0.324 |
|
| 1998 |
Corey EJ, Li W, Reichard GA. A new magnesium-catalyzed doubly diastereoselective anti-aldol reaction leads to a highly efficient process for the total synthesis of lactacystin in quantity Journal of the American Chemical Society. 120: 2330-2336. DOI: 10.1021/Ja973444C |
0.421 |
|
| 1998 |
Corey EJ, Li WDZ. An efficient total synthesis of a new and highly active analog of lactacystin Tetrahedron Letters. 39: 7475-7478. DOI: 10.1016/S0040-4039(98)01674-8 |
0.411 |
|
| 1998 |
Corey EJ, Zheng GZ. 2,6-bis(triisopropylsilyl)pyridine, an extreme example of the effect of strong steric screening on basicity Tetrahedron Letters. 39: 6151-6154. DOI: 10.1016/S0040-4039(98)01299-4 |
0.302 |
|
| 1998 |
Corey EJ, Noe MC, Xu F. Highly enantioselective synthesis of cyclic and functionalized α-amino acids by means of a chiral phase transfer catalyst Tetrahedron Letters. 39: 5347-5350. DOI: 10.1016/S0040-4039(98)01067-3 |
0.379 |
|
| 1998 |
Singh AK, Corey EJ. A Simple Synthesis of 4-Carboxyatractyligenin from Atractyligenin Journal of the Indian Chemical Society. 75: 841-842. |
0.304 |
|
| 1997 |
Corey EJ, Xu F, Noe MC. A Rational Approach to Catalytic Enantioselective Enolate Alkylation Using a Structurally Rigidified and Defined Chiral Quaternary Ammonium Salt under Phase Transfer Conditions Journal of the American Chemical Society. 119: 12414-12415. DOI: 10.1021/Ja973174Y |
0.311 |
|
| 1997 |
Corey EJ, Guzman-Perez A, Lazerwith SE. An Enantioselective Synthetic Route to Atractyligenin Using the Oxazaborolidine-Catalyzed Reduction of β-Silyl- or β-Stannyl-Substituted α,β-Enones as a Key Step Journal of the American Chemical Society. 119: 11769-11776. DOI: 10.1021/Ja973034O |
0.768 |
|
| 1997 |
Corey EJ, Luo G, Lin LS. A Simple Enantioselective Synthesis of the Biologically Active Tetracyclic Marine Sesterterpene Scalarenedial Journal of the American Chemical Society. 119: 9927-9928. DOI: 10.1021/Ja972690L |
0.391 |
|
| 1997 |
Corey EJ, Cheng H, Baker CH, Matsuda SPT, Li D, Song X. Studies on the substrate binding segments and catalytic action of lanosterol synthase. Affinity labeling with carbocations derived from mechanism-based analogs of 2,3-oxidosqualene and site-directed mutagenesis probes Journal of the American Chemical Society. 119: 1289-1296. DOI: 10.1021/Ja963228O |
0.327 |
|
| 1997 |
Corey EJ, Cheng H, Baker CH, Matsuda SPT, Li D, Song X. Methodology for the preparation of pure recombinant S. cerevisiae lanosterol synthase using a baculovirus expression system. Evidence that oxirane cleavage and A-ring formation are concerted in the biosynthesis of lanosterol from 2,3-oxidosqualene Journal of the American Chemical Society. 119: 1277-1288. DOI: 10.1021/Ja963227W |
0.411 |
|
| 1997 |
Corey EJ, Barnes-Seeman D, Lee TW. The mechanistic basis for diastereoselectivity in the Matteson rearrangement Tetrahedron-Asymmetry. 8: 3711-3713. DOI: 10.1016/S0957-4166(97)00528-4 |
0.79 |
|
| 1997 |
Corey EJ, Roberts BE. Remarkably complex and unpredictable cyclization and rearrangement reactions of cations derived from unsaturated oxiranes Tetrahedron Letters. 38: 8921-8924. DOI: 10.1016/S0040-4039(97)10426-9 |
0.366 |
|
| 1997 |
Corey EJ, Roberts BE. The Application Of A Shapiro Reaction - Suzuki Coupling Sequence To The Stereoselective Synthesis Of E-Trisubstituted Olefins Tetrahedron Letters. 38: 8919-8920. DOI: 10.1016/S0040-4039(97)10425-7 |
0.372 |
|
| 1997 |
Corey EJ, Lee J, Roberts BE. The Application Of The Shapiro Reaction To The Stereoselective Synthesis Of E-Trisubstituted Olefins For Cation-Olefin Cyclization By Three Component Coupling Tetrahedron Letters. 38: 8915-8918. DOI: 10.1016/S0040-4039(97)10424-5 |
0.362 |
|
| 1997 |
Corey EJ, Kühnle FNM. A simplified synthesis of (±)-1,2-diphenyl-1,2-diaminoethane (1) from benzaldehyde and ammonia. Revision of the structures of the long-known intermediates “hydrobenzamide” and “amarine” Tetrahedron Letters. 38: 8631-8634. DOI: 10.1016/S0040-4039(97)10372-0 |
0.323 |
|
| 1997 |
Corey EJ, Helal CJ. An Efficient Catalytic Stereoselective Route to a Key Intermediate for the Synthesis of the Long-Lived PGI2 Analog ZK 96480 (CicaprostTM) Tetrahedron Letters. 38: 7511-7514. DOI: 10.1016/S0040-4039(97)01803-0 |
0.445 |
|
| 1997 |
Corey EJ, Liu K. New Stereospecific Synthetic Routes to the Bicyclo[3.2.1]octane Subunit of the Kaurenoids and Gibberellins Tetrahedron Letters. 38: 7491-7494. DOI: 10.1016/S0040-4039(97)01798-X |
0.329 |
|
| 1997 |
Corey EJ, Azimioara MD, Fischer AK. A novel synthesis of the fluorene skeleton Tetrahedron Letters. 38: 6625-6626. DOI: 10.1016/S0040-4039(97)01534-7 |
0.741 |
|
| 1997 |
Corey EJ, Barnes-Seeman D, Lee TW, Goodman SN. A transition-state model for the Mikami enantioselective ene reaction Tetrahedron Letters. 38: 6513-6516. DOI: 10.1016/S0040-4039(97)01517-7 |
0.781 |
|
| 1997 |
Guzman-Perez A, Corey E. Allylic 4-methoxybenzoates display excellent reagent-controlled double diastereoselection in the sharpless asymmetric dihydroxylation: Application to highly selective total syntheses of polyols Tetrahedron Letters. 38: 5941-5944. DOI: 10.1016/S0040-4039(97)01327-0 |
0.412 |
|
| 1997 |
Corey EJ, Lin S, Luo G. Stereospecific Synthesis Of Tetrasubstituted Z-Enol Silyl Ethers By A Three Component Coupling Process Tetrahedron Letters. 38: 5771-5774. DOI: 10.1016/S0040-4039(97)01293-8 |
0.377 |
|
| 1997 |
Corey EJ, Lee TW. Enantioselective Diels-Alder reactions between cyclopentadiene and α,β-acetylenic aldehydes catalyzed by a chiral super Lewis acid Tetrahedron Letters. 38: 5755-5758. DOI: 10.1016/S0040-4039(97)01287-2 |
0.528 |
|
| 1997 |
Corey EJ, Barnes-Seeman D, Lee TW. The formyl C-H--O hydrogen bond as a critical factor in enantioselective reactions of aldehydes, Part 4, aldol, ethylation, hydrocyanation and Diels-Alder reactions catalyzed by chiral Bb, Ti and a1 Lewis acids Tetrahedron Letters. 38: 4351-4354. DOI: 10.1016/S0040-4039(97)00932-5 |
0.79 |
|
| 1997 |
Corey EJ, Palani A. Aromatic Annulation: Two New Methods for the Synthesis of Chiral Bicyclic Phenols Tetrahedron Letters. 38: 2397-2400. DOI: 10.1016/S0040-4039(97)00387-0 |
0.416 |
|
| 1997 |
Corey E, Zheng GZ. Catalytic reactions of samarium (II) iodide Tetrahedron Letters. 38: 2045-2048. DOI: 10.1016/S0040-4039(97)00263-3 |
0.361 |
|
| 1997 |
Corey EJ, Barnes-Seeman D, Lee TW. The formyl C-H--O hydrogen bond as a key to transition-state organization in enantioselective allylation, aldol and Diels-Alder reactions catalyzed by chiral Lewis acids Tetrahedron Letters. 38: 1699-1702. DOI: 10.1016/S0040-4039(97)00193-7 |
0.797 |
|
| 1997 |
Corey EJ, Rohde JJ. The application of the formyl C-H--O hydrogen bond postulate to the understanding of enantioselective reactions involving chiral boron Lewis acids and aldehydes Tetrahedron Letters. 38: 37-40. DOI: 10.1016/S0040-4039(96)02249-6 |
0.326 |
|
| 1997 |
Corey EJ, Rohde JJ, Fischer A, Azimioara MD. A hypothesis for conformational restriction in complexes of formyl compounds with boron Lewis acids. Experimental evidence for formyl CH--O and CH--F hydrogen bonds Tetrahedron Letters. 38: 33-36. DOI: 10.1016/S0040-4039(96)02248-4 |
0.735 |
|
| 1996 |
Corey EJ, Matsuda SP, Baker CH, Ting AY, Cheng H. Molecular cloning of a Schizosaccharomyces pombe cDNA encoding lanosterol synthase and investigation of conserved tryptophan residues. Biochemical and Biophysical Research Communications. 219: 327-31. PMID 8604986 DOI: 10.1006/Bbrc.1996.0232 |
0.577 |
|
| 1996 |
Corey EJ, Wood HB. A New Strategy for Stereocontrol of Cation−Olefin Cyclization. The First Chemical Emulation of the A/B-trans-9,10-syn-Folding Pathway of Steroid Biosynthesis from 2,3-Oxidosqualene Journal of the American Chemical Society. 118: 11982-11983. DOI: 10.1021/Ja9632926 |
0.3 |
|
| 1996 |
Corey EJ, Gin DY, Kania RS. Enantioselective total synthesis of ecteinascidin 743 Journal of the American Chemical Society. 118: 9202-9203. DOI: 10.1021/Ja962480T |
0.794 |
|
| 1996 |
Corey EJ, Noe MC. A critical analysis of the mechanistic basis of enantioselectivity in the bis-cinchona alkaloid catalyzed dihydroxylation of olefins Journal of the American Chemical Society. 118: 11038-11053. DOI: 10.1021/Ja961233M |
0.313 |
|
| 1996 |
Hayashi Y, Rohde JJ, Corey EJ. A Novel Chiral Super-Lewis Acidic Catalyst for Enantioselective Synthesis Journal of the American Chemical Society. 118: 5502-5503. DOI: 10.1021/Ja960766S |
0.64 |
|
| 1996 |
Corey EJ, Sarshar S, Azimioara MD, Newbold RC, Noe MC. X-ray crystal and NMR structure of a highly reactive bidentate 1,2-diamine-OsO4 complex, formally a 20-electron outer valence shell species. Mechanistic implications for the 1,2-diamine-accelerated dihydroxylation of olefins by OsO4 Journal of the American Chemical Society. 118: 7851-7852. DOI: 10.1021/Ja960536D |
0.727 |
|
| 1996 |
Corey EJ, Noe MC. Kinetic investigations provide additional evidence that an enzyme-like binding pocket is crucial for high enantioselectivity in the bis-cinchona alkaloid catalyzed asymmetric dihydroxylation of olefins Journal of the American Chemical Society. 118: 319-329. DOI: 10.1021/Ja952567Z |
0.307 |
|
| 1996 |
Corey EJ, Gin DY. A convergent enantioselective synthesis of the tetrahydroisoquinoline unit in the spiro ring of ecteinascidin 743 Tetrahedron Letters. 37: 7163-7166. DOI: 10.1016/0040-4039(96)01622-X |
0.784 |
|
| 1996 |
Corey EJ, Helal CJ. Asymmetric synthesis of (S)-carbinoxamine. New aspects of oxazaborolidine-catalyzed enantioselective carbonyl reduction Tetrahedron Letters. 37: 5675-5678. DOI: 10.1016/0040-4039(96)01198-7 |
0.415 |
|
| 1996 |
Corey E, Helal CJ. Catalytic enantioselective synthesis of the second generation histamine antagonist cetirizine hydrochloride Tetrahedron Letters. 37: 4837-4840. DOI: 10.1016/0040-4039(96)00964-1 |
0.436 |
|
| 1996 |
Corey EJ, Noe MC, Ting AY. Improved enantioselective dihydroxylation of bishomoallylic alcohol derivatives using a mechanistically inspired bis-cinchona alkaloid catalyst Tetrahedron Letters. 37: 1735-1738. DOI: 10.1016/0040-4039(96)00163-3 |
0.569 |
|
| 1996 |
Noe MC, Corey EJ. Position and enantioselective dihydroxylation of 2-hydroxymethyl-and 2-hydroxyethyl-1,3-butadiene derivatives using bis-cinchona alkaloid catalysts Tetrahedron Letters. 37: 1739-1742. DOI: 10.1016/0040-4039(96)00162-1 |
0.326 |
|
| 1995 |
Fenteany G, Standaert RF, Lane WS, Choi S, Corey EJ, Schreiber SL. Inhibition of proteasome activities and subunit-specific amino-terminal threonine modification by lactacystin. Science (New York, N.Y.). 268: 726-31. PMID 7732382 DOI: 10.1126/Science.7732382 |
0.705 |
|
| 1995 |
Baker CH, Matsuda SP, Liu DR, Corey EJ. Molecular cloning of the human gene encoding lanosterol synthase from a liver cDNA library. Biochemical and Biophysical Research Communications. 213: 154-60. PMID 7639730 DOI: 10.1006/Bbrc.1995.2110 |
0.482 |
|
| 1995 |
Corey EJ, Letavic MA. Enantioselective Total Synthesis of Gracilins B and C Using Catalytic Asymmetric Diels-Alder Methodology. [Erratum to document cited in CA123:340457] Journal of the American Chemical Society. 117: 12017-12017. DOI: 10.1021/Ja00153A033 |
0.345 |
|
| 1995 |
Corey EJ, Virgil SC, Cheng H, Baker CH, Matsuda SPT, Singh V, Sarshar S. New insights regarding the cyclization pathway for sterol biosynthesis from (S)-2,3-oxidosqualene Journal of the American Chemical Society. 117: 11819-11820. DOI: 10.1021/Ja00152A030 |
0.595 |
|
| 1995 |
Corey EJ, Noe MC, Guzman-Perez A. Kinetic resolution by enantioselective dihydroxylation of secondary allylic 4-methoxybenzoate esters using a mechanistically designed cinchona alkaloid catalyst Journal of the American Chemical Society. 117: 10817-10824. DOI: 10.1021/Ja00149A004 |
0.336 |
|
| 1995 |
Corey EJ, Letavic MA. Enantioselective Total Synthesis Of Gracilins B And C Using Catalytic Asymmetric Diels-Alder Methodology Journal of the American Chemical Society. 117: 9616-9617. DOI: 10.1021/Ja00142A051 |
0.402 |
|
| 1995 |
Corey EJ, Roberts BE, Dixon BR. Enantioselective Total Synthesis of .beta.-Elemene and Fuscol Based on Enantiocontrolled Ireland-Claisen Rearrangement Journal of the American Chemical Society. 117: 193-196. DOI: 10.1021/Ja00106A023 |
0.317 |
|
| 1995 |
Corey EJ, Lee D, Sarshar S. Convenient routes to symmetrical benzils and chiral 1,2-diaryl-1,2-diaminoethanes, useful controllers and probes for enantioselective synthesis Tetrahedron-Asymmetry. 6: 3-6. DOI: 10.1016/0957-4166(94)00336-A |
0.401 |
|
| 1995 |
Corey E, Helal CJ. Novel electronic effects of remote substituents on the oxazaborolidine-catalyzed enantioselective reduction of ketones Tetrahedron Letters. 36: 9153-9156. DOI: 10.1016/0040-4039(95)01961-G |
0.353 |
|
| 1995 |
Gant TG, Noe MC, Corey EJ. The first enantioselective synthesis of the chemotactic factor sirenin by an intramolecular [2 + 1] cyclization using a new chiral catalyst Tetrahedron Letters. 36: 8745-8748. DOI: 10.1016/0040-4039(95)01924-7 |
0.415 |
|
| 1995 |
Corey EJ, Noe MC, Lin S. A mechanistically designed bis-cinchona alkaloid ligand allows position- and enantioselective dihydroxylation of farnesol and other oligoprenyl derivatives at the terminal isopropylidene unit Tetrahedron Letters. 36: 8741-8744. DOI: 10.1016/0040-4039(95)01920-D |
0.321 |
|
| 1995 |
Corey EJ, Noe MC, Guzman-Perez A. Catalytic enantioselective synthesis of (14R)-14-hydroxy-4,14-retro-retinol from retinyl acetate Tetrahedron Letters. 36: 4171-4174. DOI: 10.1016/0040-4039(95)00774-7 |
0.377 |
|
| 1994 |
Fenteany G, Standaert RF, Reichard GA, Corey EJ, Schreiber SL. A beta-lactone related to lactacystin induces neurite outgrowth in a neuroblastoma cell line and inhibits cell cycle progression in an osteosarcoma cell line. Proceedings of the National Academy of Sciences of the United States of America. 91: 3358-62. PMID 8159752 DOI: 10.1073/Pnas.91.8.3358 |
0.706 |
|
| 1994 |
Corey EJ, Guzman-Perez A, Noe MC. Short enantioselective synthesis of (-)-ovalicin, a potent inhibitor of angiogenesis, using substrate-enhanced catalytic asymmetric dihydroxylation Journal of the American Chemical Society. 116: 12109-12110. DOI: 10.1021/Ja00105A084 |
0.362 |
|
| 1994 |
Corey EJ, Sarshar S, Lee D. First Example of a Highly Enantioselective Catalytic Diels-Alder Reaction of an Achiral C2v-Symmetric Dienophile and an Achiral Diene Journal of the American Chemical Society. 116: 12088-12090. DOI: 10.1021/Ja00105A074 |
0.354 |
|
| 1994 |
Corey EJ, Rao SA, Noe MC. Catalytic diastereoselective synthesis of cis-1,2-disubstituted cyclopropanols from esters using a vicinal dicarbanion equivalent Journal of the American Chemical Society. 116: 9345-9346. DOI: 10.1021/Ja00099A068 |
0.397 |
|
| 1994 |
Corey EJ, Guzman-Perez A, Loh T. Demonstration of the Synthetic Power of Oxazaborolidine-Catalyzed Enantioselective Diels-Alder Reactions by Very Efficient Routes to Cassiol and Gibberellic Acid Journal of the American Chemical Society. 116: 3611-3612. DOI: 10.1021/Ja00087A062 |
0.526 |
|
| 1994 |
Corey EJ, Cimprich KA. Highly Enantioselective Alkynylation of Aldehydes Promoted by Chiral Oxazaborolidines Journal of the American Chemical Society. 116: 3151-3152. DOI: 10.1021/Ja00086A066 |
0.353 |
|
| 1994 |
Corey EJ, Hong BC. Chemical emulation of the biosynthetic route to glycinoeclepin from a cycloartenol derivative Journal of the American Chemical Society. 116: 3149-3150. DOI: 10.1021/Ja00086A065 |
0.604 |
|
| 1994 |
Corey EJ, Chen Z. Enantioselective synthesis of γ-hydroxysilanes, 1,3-diols and cyclopropanes by reaction of a chiral epoxide with a racemic α-silyl organolithium reagent Tetrahedron Letters. 35: 8731-8734. DOI: 10.1016/S0040-4039(00)78483-8 |
0.37 |
|
| 1994 |
Corey EJ, Noe MC, Grogan MJ. A mechanistically designed mono-cinchona alkaloid is an excellent catalyst for the enantioselective dihydroxylation of olefins Tetrahedron Letters. 35: 6427-6430. DOI: 10.1016/S0040-4039(00)78237-2 |
0.34 |
|
| 1994 |
Corey E, Wang Z. Conversion of arachidonic acid to the prostaglandin endoperoxide PGG2, a chemical analog of the biosynthetic pathway Tetrahedron Letters. 35: 539-542. DOI: 10.1016/S0040-4039(00)75832-1 |
0.35 |
|
| 1994 |
Corey EJ, Gant TG. A catalytic enantioselective synthetic route to the important antidepressant sertraline Tetrahedron Letters. 35: 5373-5376. DOI: 10.1016/S0040-4039(00)73503-9 |
0.391 |
|
| 1994 |
Corey E, Lee J, Liu DR. First demonstration of a carbocation-olefin cyclization route to the lanosterol series Tetrahedron Letters. 35: 9149-9152. DOI: 10.1016/0040-4039(94)88450-1 |
0.559 |
|
| 1994 |
Corey EJ, Cywin CL, Noe MC. Synthesis and X-ray structure of a novel chiral trinuclear titanium-tetraol complex Tetrahedron Letters. 35: 69-72. DOI: 10.1016/0040-4039(94)88164-2 |
0.323 |
|
| 1993 |
Corey EJ, Loh TP, AchyuthaRao S, Daley DC, Sarshar S. Stereocontrolled total synthesis of (+)- and (-)-epibatidine Journal of Organic Chemistry. 58: 5600-5602. DOI: 10.1021/Jo00073A013 |
0.42 |
|
| 1993 |
Corey EJ, Chen Z, Tanoury GJ. A new and highly enantioselective synthetic route to P-chiral phosphines and diphosphines Journal of the American Chemical Society. 115: 11000-11001. DOI: 10.1021/Ja00076A072 |
0.339 |
|
| 1993 |
Corey EJ, Wu LI. Enantioselective total synthesis of miroestrol Journal of the American Chemical Society. 115: 9327-9328. DOI: 10.1021/Ja00073A074 |
0.443 |
|
| 1993 |
Corey EJ, Lee J. Enantioselective total synthesis of oleanolic acid, erythrodiol, .beta.-amyrin, and other pentacyclic triterpenes from a common intermediate Journal of the American Chemical Society. 115: 8873-8874. DOI: 10.1021/Ja00072A064 |
0.355 |
|
| 1993 |
Corey EJ, Wu YJ. Total synthesis of (.+-.)-paeoniflorigenin and paeoniflorin Journal of the American Chemical Society. 115: 8871-8872. DOI: 10.1021/Ja00072A063 |
0.421 |
|
| 1993 |
Corey EJ, Daigneault S, Dixon BR. A biomimetic chemical synthesis of humulene from farnesol Tetrahedron Letters. 34: 3675-3678. DOI: 10.1016/S0040-4039(00)79198-2 |
0.437 |
|
| 1993 |
Corey E, Helal CJ. A catalytic enantioselective synthesis of chiral monosubstituted oxiranes Tetrahedron Letters. 34: 5227-5230. DOI: 10.1016/S0040-4039(00)73959-1 |
0.442 |
|
| 1993 |
Corey EJ, Noe MC, Wen-Chung S. A short and convergent enantioselective synthesis of (3S)-2,3-oxidosqualene Tetrahedron Letters. 34: 5995-5998. DOI: 10.1016/S0040-4039(00)61710-0 |
0.375 |
|
| 1993 |
Corey EJ, Reichard GA, Kania R. Studies on the total synthesis of lactacystin. An improved aldol coupling reaction and a β-lactone intermediate in thiol ester formation Tetrahedron Letters. 34: 6977-6980. DOI: 10.1016/S0040-4039(00)61575-7 |
0.37 |
|
| 1993 |
Corey EJ, Reichard GA. Synthesis of (6R,7S)-lactacystin and 6-deoxylactacystin from a common intermediate Tetrahedron Letters. 34: 6973-6976. DOI: 10.1016/S0040-4039(00)61574-5 |
0.307 |
|
| 1993 |
Corey EJ, Choi S. An enantioselective synthesis of (6R)-lactacystin Tetrahedron Letters. 34: 6969-6972. DOI: 10.1016/S0040-4039(00)61573-3 |
0.334 |
|
| 1993 |
Corey E, Roper TD, Ishihara K, Sarakinos G. Catalytic enantioselective Diels-Alder reactions using titanium complexes of cis-N-sulfonyl-2-amino-1-indanols Tetrahedron Letters. 34: 8399-8402. DOI: 10.1016/S0040-4039(00)61343-6 |
0.79 |
|
| 1993 |
Corey E, Lee D. The E/Z geometry of the enolate component determines face selection of the aldehyde component in chiral diazaborolidine-directed enantioselective aldol coupling Tetrahedron Letters. 34: 1737-1740. DOI: 10.1016/S0040-4039(00)60765-7 |
0.359 |
|
| 1993 |
Corey EJ, Zhe W. Enantioselective conversion of aldehydes to cyanohydrins by a catalytic system with separate chiral binding sites for aldehyde and cyanide components Tetrahedron Letters. 34: 4001-4004. DOI: 10.1016/S0040-4039(00)60600-7 |
0.382 |
|
| 1993 |
Corey E, Loh T. Catalytic enantioselective diels-alder addition to furan provides a direct synthetic route to many chiral natural products Tetrahedron Letters. 34: 3979-3982. DOI: 10.1016/S0040-4039(00)60594-4 |
0.578 |
|
| 1993 |
Corey EJ, Houpis IN. The control of diastereoselectivity in the Michael reaction of ketonic enolates with crotonic acid derivatives Tetrahedron Letters. 34: 2421-2424. DOI: 10.1016/S0040-4039(00)60431-8 |
0.409 |
|
| 1992 |
Corey EJ, Rao KS, Ghosh AK. INTRAMOLECULAR AND INTERMOLECULAR HYDROXYL REACTIVITY DIFFERENCES IN GINKGOLIDES A, B AND C AND THEIR CHEMICAL APPLICATIONS. Tetrahedron Letters. 33: 6955-6958. PMID 30310244 DOI: 10.1016/S0040-4039(00)60905-X |
0.545 |
|
| 1992 |
Corey EJ, Cywin CL. A simple enantioselective synthesis of (1S,4R)-bicyclo[2.2.1]hept-2-ene-2-methanol Journal of Organic Chemistry. 57: 7372-7373. DOI: 10.1021/Jo00052A072 |
0.338 |
|
| 1992 |
Corey EJ, Jones GB. Reductive cleavage of tert-butyldimethylsilyl ethers by diisobutylaluminum hydride Journal of Organic Chemistry. 57: 1028-1029. DOI: 10.1021/Jo00029A050 |
0.326 |
|
| 1992 |
Corey EJ, Reichard GA. Total synthesis of lactacystin Journal of the American Chemical Society. 114: 10677-10678. DOI: 10.1021/Ja00052A096 |
0.421 |
|
| 1992 |
Corey EJ, Loh TP, Roper TD, Azimioara MD, Noe MC. The origin of greater than 200:1 enantioselectivity in a catalytic Diels-Alder reaction as revealed by physical and chemical studies Journal of the American Chemical Society. 114: 8290-8292. DOI: 10.1021/Ja00047A050 |
0.773 |
|
| 1992 |
Corey EJ, Sarshar S, Bordner J. X-ray crystallographic and NMR studies on the origins of high enantioselectivity in diels-alder reactions catalyzed by a chiral diazaaluminolidine Journal of the American Chemical Society. 114: 7938-7939. DOI: 10.1021/Ja00046A065 |
0.321 |
|
| 1992 |
Corey EJ, Link JO. A general, catalytic, and enantioselective synthesis of .alpha.-amino acids Journal of the American Chemical Society. 114: 1906-1908. DOI: 10.1021/Ja00031A069 |
0.367 |
|
| 1992 |
Corey EJ, Virgil SC, Liu DR, Sarshar S. The methyl group at C(10) of 2,3-oxidosqualene is crucial to the correct folding of this substrate in the cyclization-rearrangement step of sterol biosynthesis Journal of the American Chemical Society. 114: 1524-1525. DOI: 10.1021/Ja00030A083 |
0.466 |
|
| 1992 |
Corey E, Link JO, Shao Y. Two effective procedures for the synthesis of trichloromethyl ketones, useful precursors of chiral α-amino and α-hydroxy acids Tetrahedron Letters. 33: 3435-3438. DOI: 10.1016/S0040-4039(00)92656-X |
0.404 |
|
| 1992 |
Corey E, Link JO. A new process for the enantioselective synthesis of chiral α-aryloxy- and α-hydroxy acids Tetrahedron Letters. 33: 3431-3434. DOI: 10.1016/S0040-4039(00)92655-8 |
0.368 |
|
| 1992 |
Corey EJ, Azimioara M, Sarshar S. X-Ray crystal structure of a chiral oxazaborolidine catalyst for enantioselective carbonyl reduction Tetrahedron Letters. 33: 3429-3430. DOI: 10.1016/S0040-4039(00)92654-6 |
0.74 |
|
| 1992 |
Corey E, Shieh W. A simple synthetic process for the elaboration of oligoprenols by stereospecific coupling of di-, tri-, or oligoisoprenoid units Tetrahedron Letters. 33: 6435-6438. DOI: 10.1016/S0040-4039(00)79008-3 |
0.317 |
|
| 1992 |
Corey E, Link JO. A new process for the generation of 1,3,2-oxazaborolidines, catalysts for enantioselective synthesis Tetrahedron Letters. 33: 4141-4144. DOI: 10.1016/S0040-4039(00)74673-9 |
0.381 |
|
| 1992 |
Corey EJ, Cimprich KA. Enantioselective routes to chiral benzylic thiols, sulfinic esters and sulfonic acids illustrated by the 1-phenylethyl series Tetrahedron Letters. 33: 4099-4102. DOI: 10.1016/S0040-4039(00)74662-4 |
0.695 |
|
| 1992 |
Corey EJ, Yi KY, Matsuda SPT. Catalytic enatioselective synthesis of (3S)-2,3-oxidosqualene Tetrahedron Letters. 33: 2319-2322. DOI: 10.1016/S0040-4039(00)74200-6 |
0.405 |
|
| 1992 |
Corey E, Ishihara K. Highly enantioselective catalytic Diels-Alder addition promoted by a chiral bis(oxazoline)-magnesium complex Tetrahedron Letters. 33: 6807-6810. DOI: 10.1016/S0040-4039(00)61781-1 |
0.535 |
|
| 1992 |
Corey EJ, Loh TP, Sarshar S, Azimioara M. The structure of the 2-methylacrolein boron trifluoride complex in the crystalline phase and in solution Tetrahedron Letters. 33: 6945-6948. DOI: 10.1016/S0040-4039(00)60902-4 |
0.774 |
|
| 1992 |
Corey EJ, Cywin CL, Roper TD. Enantioselective Mukaiyama-aldol and aldol-dihydropyrone annulation reactions catalyzed by a tryptophan-derived oxazaborolidine Tetrahedron Letters. 33: 6907-6910. DOI: 10.1016/S0040-4039(00)60892-4 |
0.753 |
|
| 1992 |
Corey E, Link JO, Bakshi RK. A mechanistic and structural analysis of the basis for high enantioselectivity in the oxazaborolidine-catalyzed reduction of trihalomethyl ketones by catecholborane Tetrahedron Letters. 33: 7107-7110. DOI: 10.1016/S0040-4039(00)60848-1 |
0.328 |
|
| 1991 |
Bansal R, Cooper GF, Corey EJ. Stereoselective synthesis of an important prostaglandin synthetic intermediate Journal of Organic Chemistry. 56: 1329-1332. DOI: 10.1021/Jo00003A083 |
0.355 |
|
| 1991 |
Corey EJ, Link JO. A Catalytic Enantioselective Synthesis Of Denopamine, A Useful Drug For Congestive Heart Failure Journal of Organic Chemistry. 56: 442-444. DOI: 10.1021/Jo00001A084 |
0.355 |
|
| 1991 |
Corey EJ, Loh TP. First application of attractive intramolecular interactions to the design of chiral catalysts for highly enantioselective Diels-Alder reactions Journal of the American Chemical Society. 113: 8966-8967. DOI: 10.1021/Ja00023A066 |
0.323 |
|
| 1991 |
Corey EJ, Imai N, Zhang HY. Designed catalyst for enantioselective Diels-Alder addition from a C2-symmetric chiral bis(oxazoline)-iron(III) complex Journal of the American Chemical Society. 113: 728-729. DOI: 10.1021/Ja00002A081 |
0.306 |
|
| 1991 |
Corey EJ, Jones GB. Enantioselective route to α-hydroxy aldehyde and acid derivatives Tetrahedron Letters. 32: 5713-5716. DOI: 10.1016/S0040-4039(00)93537-8 |
0.416 |
|
| 1991 |
Corey EJ, Kigoshi H. A route for the enantioselective total synthesis of antheridic acid, the antheridium-inducing factor from anemia phyllitidis Tetrahedron Letters. 32: 5025-5028. DOI: 10.1016/S0040-4039(00)93418-X |
0.433 |
|
| 1991 |
Corey EJ, Decicco CP, Newbold RC. Highly enantioselective and diastereoselective synthesis of β-amino acid esters and β-lactams from achiral esters and imines Tetrahedron Letters. 32: 5287-5290. DOI: 10.1016/S0040-4039(00)92366-9 |
0.361 |
|
| 1991 |
Corey E, Rao K. Enantioselective total synthesis of ginkgolide derivatives lacking the tert-butyl group, an essential structural subunit for antagonism of platelet activating factor Tetrahedron Letters. 32: 4623-4626. DOI: 10.1016/S0040-4039(00)92265-2 |
0.345 |
|
| 1991 |
Corey E, Sodeoka M. An effective system for epoxide-initiated cation-olefin cyclization Tetrahedron Letters. 32: 7005-7008. DOI: 10.1016/0040-4039(91)85025-Z |
0.544 |
|
| 1991 |
Corey EJ, Choi S. Highly enantioselective routes to Darzens and acetate aldol products from achiral aldehydes and t-butyl bromoacetate Tetrahedron Letters. 32: 2857-2860. DOI: 10.1016/0040-4039(91)80631-F |
0.365 |
|
| 1991 |
Corey EJ, Imai N, Pikul S. Catalytic enantioselective synthesis of a key intermediate for the synthesis of prostanoids Tetrahedron Letters. 32: 7517-7520. DOI: 10.1016/0040-4039(91)80522-8 |
0.394 |
|
| 1991 |
Corey EJ, Cheng XM, Cimprich KA. 1-Mesityl-2,2,2-trifluoroethanol, an outstanding new chiral controller for catalyzed diels-alder reactions Tetrahedron Letters. 32: 6839-6842. DOI: 10.1016/0040-4039(91)80420-B |
0.667 |
|
| 1991 |
Corey EJ, Cheng XM, Cimprich KA, Sarshar S. Remarkably effective and simple syntheses of enantiomerically pure secondary carbinols from achiral ketones Tetrahedron Letters. 32: 6835-6838. DOI: 10.1016/0040-4039(91)80419-7 |
0.688 |
|
| 1991 |
Corey EJ, Matsumura Y. Evidence for the importance of π-π-attractive interactions in Enantioselective Diels-Alder reactions chiral catalysts of type (RO)2TiCl2 Tetrahedron Letters. 32: 6289-6292. DOI: 10.1016/0040-4039(91)80149-Z |
0.336 |
|
| 1991 |
Corey EJ. The Logic of Chemical Synthesis: Multistep Synthesis of Complex Carbogenic Molecules(Nobel Lecture) Angewandte Chemie International Edition in English. 30: 455-465. DOI: 10.1002/Anie.199104553 |
0.362 |
|
| 1991 |
Corey EJ. Die Logik der chemischen Synthese: Vielstufige Synthesen komplexer „carbogener” Moleküle (Nobel-Vortrag) Angewandte Chemie. 103: 469-479. DOI: 10.1002/Ange.19911030504 |
0.356 |
|
| 1990 |
Corey EJ, Wright SW. Total synthesis of colneleic acid Journal of Organic Chemistry. 55: 1670-1673. DOI: 10.1021/Jo00292A049 |
0.304 |
|
| 1990 |
Corey EJ, Yuen PW, Hannon FJ, Wierda DA. Polyfunctional, structurally defined catalysts for the enantioselective addition of dialkylzinc reagents to aldehydes Journal of Organic Chemistry. 55: 784-786. DOI: 10.1021/Jo00290A002 |
0.332 |
|
| 1990 |
Corey EJ, Houpis IN. Total synthesis of glycinoeclepin A Journal of the American Chemical Society. 112: 8997-8998. DOI: 10.1021/Ja00180A064 |
0.415 |
|
| 1990 |
Corey EJ, Virgil SC. Enantioselective total synthesis of a protosterol, 3.beta.,20-dihydroxyprotost-24-ene Journal of the American Chemical Society. 112: 6429-6431. DOI: 10.1021/Ja00173A059 |
0.318 |
|
| 1990 |
Corey EJ, Kim SS. Versatile chiral reagent for the highly enantioselective synthesis of either anti or syn ester aldols Journal of the American Chemical Society. 112: 4976-4977. DOI: 10.1021/Ja00168A062 |
0.42 |
|
| 1990 |
Corey EJ, Yu CM, Lee DH. A practical and general enantioselective synthesis of chiral propa-1,2-dienyl and propargyl carbinols Journal of the American Chemical Society. 112: 878-879. DOI: 10.1021/Ja00158A064 |
0.36 |
|
| 1990 |
Corey EJ, Carpino P. A new enantiospecific route to the pseudopterosins Tetrahedron Letters. 31: 3857-3858. DOI: 10.1016/S0040-4039(00)97487-2 |
0.399 |
|
| 1990 |
Corey EJ, Wei-guo S. Total synthesis of a potent thromboxane A2 antagonist Tetrahedron Letters. 31: 3833-3836. DOI: 10.1016/S0040-4039(00)97481-1 |
0.33 |
|
| 1990 |
Corey E, Carpino P. A simplified synthesis of (+)-brefeldin A Tetrahedron Letters. 31: 7555-7558. DOI: 10.1016/S0040-4039(00)97297-6 |
0.431 |
|
| 1990 |
Corey EJ, Wei-guo S. Identification of a crucial substructural unit for thromboxane A2 receptor binding Tetrahedron Letters. 31: 2677-2680. DOI: 10.1016/S0040-4039(00)94670-7 |
0.3 |
|
| 1990 |
Corey EJ, Lotto GI. The origin of enantioselectivity in the dihydroxylation of olefins by osmium tetroxide and cinchona alkaloid derivatives Tetrahedron Letters. 31: 2665-2668. DOI: 10.1016/S0040-4039(00)94667-7 |
0.377 |
|
| 1990 |
Corey EJ, Bakshi RK. A new system for catalytic enantioselective reduction of achiral ketones to chiral alcohols. Synthesis of chiral α-hydroxy acids Tetrahedron Letters. 31: 611-614. DOI: 10.1016/S0040-4039(00)94581-7 |
0.383 |
|
| 1990 |
Corey E, Link JO. The first enantioselective syntheses of pure R- and S-isoproterenol Tetrahedron Letters. 31: 601-604. DOI: 10.1016/S0040-4039(00)94578-7 |
0.326 |
|
| 1990 |
Corey EJ, Kamiyama K. A simple stereoselective synthesis of a tetracyclic C14 ginkgolide Tetrahedron Letters. 31: 3995-3998. DOI: 10.1016/S0040-4039(00)94481-2 |
0.401 |
|
| 1989 |
Corey EJ, Posner GH, Atkinson RF, Wingard AK, Halloran DJ, Radzik DM, Nash JJ. Formation of olefins via pyrolysis of sulfonate esters The Journal of Organic Chemistry. 54: 389-393. DOI: 10.1021/Jo00263A024 |
0.533 |
|
| 1989 |
Corey EJ, Jardine PD, Virgil S, Yuen PW, Connell RD. Enantioselective vicinal hydroxylation of terminal and E-1,2-disubstituted olefins by a chiral complex of osmium tetroxide. An effective controller system and a rational mechanistic model Journal of the American Chemical Society. 111: 9243-9244. DOI: 10.1021/Ja00208A025 |
0.355 |
|
| 1989 |
Corey EJ, Yu CM, Kim SS. A practical and efficient method for enantioselective allylation of aldehydes Journal of the American Chemical Society. 111: 5495-5496. DOI: 10.1021/Ja00196A082 |
0.343 |
|
| 1989 |
Corey E, Link JO. A new chiral catalyst for the enantioselective synthesis of secondary alcohols and deuterated primary alcohols by carbonyl reduction Tetrahedron Letters. 30: 6275-6278. DOI: 10.1016/S0040-4039(01)93871-7 |
0.352 |
|
| 1989 |
Corey EJ, Chen C-, Reichard GA. (+)-1(S), 5(R), 8(S)-8-phenyl-2-azabicyclo[3.3.0]octan-8-ol n,o-methylboronate (2) and its enantiomer, chiral chemzymes which serve as catalysts for their own enantioselective synthesis Tetrahedron Letters. 30: 5547-5550. DOI: 10.1016/S0040-4039(01)93796-7 |
0.388 |
|
| 1989 |
Corey E, Huang H. Enantioselective synthesis of the C(18) – C(35) segment of immunosuppressant FK-506 using efficient new methodology Tetrahedron Letters. 30: 5235-5238. DOI: 10.1016/S0040-4039(01)93750-5 |
0.393 |
|
| 1989 |
Corey EJ, Ohtani M. Enantiospecific synthesis of a rigid, C2 symmetric, chiral guanidine by a new and direct method Tetrahedron Letters. 30: 5227-5230. DOI: 10.1016/S0040-4039(01)93748-7 |
0.419 |
|
| 1989 |
Corey EJ, Reichard GA. Enantioselective and practical syntheses of R- and S-fluoxetines Tetrahedron Letters. 30: 5207-5210. DOI: 10.1016/S0040-4039(01)93743-8 |
0.332 |
|
| 1989 |
Corey EJ, Yuen P. A short, stereospecific route to chiral trans-2,6-disubstituted quinuclidines Tetrahedron Letters. 30: 5825-5828. DOI: 10.1016/S0040-4039(01)93481-1 |
0.448 |
|
| 1989 |
Corey EJ, Su W, Cleaver MB. A simple and efficient synthesis of (7E, 9E, 11Z, 13E)-(5S, 6R, 15S)-trihydroxyeicosatetraenoic acid (6R-lipoxin A) Tetrahedron Letters. 30: 4181-4184. DOI: 10.1016/S0040-4039(01)80684-5 |
0.315 |
|
| 1989 |
Corey E, Hahl RW. Synthesis of a limonoid, azadiradione Tetrahedron Letters. 30: 3023-3026. DOI: 10.1016/S0040-4039(00)99392-4 |
0.434 |
|
| 1989 |
Corey EJ, Jardine PDS. A short and efficient enantioselective route to a key intermediate for the total synthesis of forskolin Tetrahedron Letters. 30: 7297-7300. DOI: 10.1016/S0040-4039(00)70681-2 |
0.455 |
|
| 1989 |
Corey EJ, Hannon FJ, Boaz NW. Coordinattvely induced 1,4-diastereoselection in the reaction of acyclic α,β-enones with organocopper reagents. A new type of organocopper reagent Tetrahedron. 45: 545-555. DOI: 10.1016/0040-4020(89)80082-1 |
0.669 |
|
| 1988 |
Corey EJ, Ghosh AK. TOTAL SYNTHESIS OF GINKGOLIDE A. Tetrahedron Letters. 29: 3205-3206. PMID 31595095 DOI: 10.1016/0040-4039(88)85122-0 |
0.601 |
|
| 1988 |
Corey EJ, Kang MC, Desai MC, Ghosh AK, Houpis IN. Total Synthesis of (±)-Ginkgolide B. Journal of the American Chemical Society. 110: 649-651. PMID 31527923 DOI: 10.1021/Ja00210A083 |
0.553 |
|
| 1988 |
Corey EJ, Shibata S, Bakshi RK. An efficient and catalytically enantioselective route to (S)-(-)-phenyloxirane The Journal of Organic Chemistry. 53: 2861-2863. DOI: 10.1021/Jo00247A044 |
0.33 |
|
| 1988 |
Corey EJ, Jardine PDS, Mohri T. Enantioselective route to a key intermediate in the total synthesis of forskolin Tetrahedron Letters. 29: 6409-6412. DOI: 10.1016/S0040-4039(00)82359-X |
0.406 |
|
| 1988 |
Corey EJ, Xiang YB. Enantioselective total synthesis of (−)-preclavulone-A Tetrahedron Letters. 29: 995-998. DOI: 10.1016/0040-4039(88)85317-6 |
0.376 |
|
| 1988 |
Corey EJ, Su W. Enantioselective total synthesis of bilobalide, A C15 ginkgolide Tetrahedron Letters. 29: 3423-3426. DOI: 10.1016/0040-4039(88)85179-7 |
0.449 |
|
| 1988 |
Corey E, Gavai AV. Enantioselective route to a key intermediate in the total synthesis of ginkgolide B Tetrahedron Letters. 29: 3201-3204. DOI: 10.1016/0040-4039(88)85121-9 |
0.391 |
|
| 1988 |
Corey EJ, Ha DC. Total synthesis of venustatriol Tetrahedron Letters. 29: 3171-3174. DOI: 10.1016/0040-4039(88)85113-X |
0.438 |
|
| 1988 |
Corey EJ, Mehrotra MM. A simple and enantioselective synthesis of (+)-biotin Tetrahedron Letters. 29: 57-60. DOI: 10.1016/0040-4039(88)80015-7 |
0.39 |
|
| 1987 |
Corey EJ, Ghosh AK. Two-Step Synthesis of Furans by Mn(III)-Promoted Annulation of Enol Ethers. Chemistry Letters. 16: 223-226. PMID 31595102 DOI: 10.1246/Cl.1987.223 |
0.624 |
|
| 1987 |
Corey EJ, Ghosh AK. Mn(III)-PROMOTED ANNULATION OF ENOL ETHERS AND ESTERS TO FUSED OR SPIRO 2-CYCLOPENTENONES. Tetrahedron Letters. 28: 175-178. PMID 31595094 DOI: 10.1016/S0040-4039(00)95679-X |
0.627 |
|
| 1987 |
d'Alarcao M, Corey EJ, Cunard C, Ramwell P, Uotila P, Vargas R, Wroblewska B. The vasodilatation induced by hydroperoxy metabolites of arachidonic acid in the rat mesenteric and pulmonary circulation. British Journal of Pharmacology. 91: 627-32. PMID 3607370 DOI: 10.1111/J.1476-5381.1987.Tb11256.X |
0.672 |
|
| 1987 |
Chang M, Rao MK, Reddanna P, Li CH, Tu CPD, Corey EJ, Reddy CC. I. Specificity of the glutathione S-transferases in the conversion of leukotriene A4 to leukotriene C4 Archives of Biochemistry and Biophysics. 259: 536-547. PMID 2827579 DOI: 10.1016/0003-9861(87)90520-0 |
0.301 |
|
| 1987 |
Corey EJ, Bakshi RK, Shibata S, Chen CP, Singh VK. A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses Journal of the American Chemical Society. 109: 7925-7926. DOI: 10.1021/Ja00259A075 |
0.596 |
|
| 1987 |
Corey EJ, Su WG. Total synthesis of a C15 ginkgolide, (.+-.)-bilobalide Journal of the American Chemical Society. 109: 7534-7536. DOI: 10.1021/Ja00258A050 |
0.358 |
|
| 1987 |
Corey EJ, Bakshi RK, Shibata S. Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications Journal of the American Chemical Society. 109: 5551-5553. DOI: 10.1021/Ja00252A056 |
0.387 |
|
| 1987 |
Corey EJ, Wess G, Xiang YB, Singh AK. Stereospecific total synthesis of (.+-.)-cafestol Journal of the American Chemical Society. 109: 4717-4718. DOI: 10.1021/Ja00249A043 |
0.424 |
|
| 1987 |
Corey EJ, Reid JG, Myers AG, Hahl RW. Simple synthetic route to the limonoid system Journal of the American Chemical Society. 109: 918-919. DOI: 10.1021/Ja00237A058 |
0.658 |
|
| 1987 |
Corey EJ, D'Alarcao M, Matsuda SPT, Lansbury PT, Yamada Y. Intermediacy of 8-(R)-HPETE in the conversion of arachidonic acid to pre-clavulone a by Clavularia viridis. Implications for the biosynthesis of marine prostanoids Journal of the American Chemical Society. 109: 289-290. DOI: 10.1021/Ja00235A053 |
0.687 |
|
| 1987 |
Corey EJ, Magriotis PA. Total synthesis and absolute configuration of 7,20-diisocyanoadociane Journal of the American Chemical Society. 109: 287-289. DOI: 10.1021/Ja00235A052 |
0.414 |
|
| 1987 |
Corey E, Burk RM. Total synthesis of (±)-tricyclohexaprenol, a possible forerunner of sterols in the evolution of biomembranes Tetrahedron Letters. 28: 6413-6416. DOI: 10.1016/S0040-4039(00)96875-8 |
0.328 |
|
| 1987 |
Corey EJ, Xiang YB. A method for the off-ring functionalization of carbon-substituted furans. Synthesis of kahweol from cafestol Tetrahedron Letters. 28: 5403-5406. DOI: 10.1016/S0040-4039(00)96739-X |
0.38 |
|
| 1987 |
Corey EJ, Nagata R. Synthesis of three new dehydroarachidonic acid derivatives and their oxidation by soybean lipoxygenase Tetrahedron Letters. 28: 5391-5394. DOI: 10.1016/S0040-4039(00)96736-4 |
0.381 |
|
| 1987 |
Corey EJ, Su W. A novel, one-step annulation process for the synthesis of ring-fused 2-cyclopentenones Tetrahedron Letters. 28: 5241-5244. DOI: 10.1016/S0040-4039(00)96697-8 |
0.425 |
|
| 1987 |
Corey EJ, Hannon FJ. Zinc complexes of chiral phenols as catalysts for enantioselective addition of organozinc reagents to aldehydes Tetrahedron Letters. 28: 5237-5240. DOI: 10.1016/S0040-4039(00)96696-6 |
0.34 |
|
| 1987 |
Corey EJ, Hannon FJ. Chiral catalysts for the enantioselective addition of organometallic reagents to aldehydes Tetrahedron Letters. 28: 5233-5236. DOI: 10.1016/S0040-4039(00)96695-4 |
0.334 |
|
| 1987 |
Corey EJ, Seibel WL, Kappos JC. Mechanism of the nitrous acid-induced dealkylation of trisubstituted (terminal isopropylidene) olefins to form acetylenes Tetrahedron Letters. 28: 4921-4924. DOI: 10.1016/S0040-4039(00)96659-0 |
0.315 |
|
| 1987 |
Corey EJ, Nagata R, Wright SW. Biomimetic total synthesis of colneleic acid and its function as a lipoxygenase inhibitor Tetrahedron Letters. 28: 4917-4920. DOI: 10.1016/S0040-4039(00)96658-9 |
0.334 |
|
| 1987 |
Corey E, Ritter K, Yus M, Nájera C. Biomimetic synthesis of a preclavulone a model Tetrahedron Letters. 28: 3547-3550. DOI: 10.1016/S0040-4039(00)95531-X |
0.499 |
|
| 1987 |
Yamane H, Nohara K, Takahashi N, Corey E, Myers AG, Schraudolft H, Takeno K. Biological activity of antheridic acid, an antheridiogen of anemia phyllitidis Phytochemistry. 26: 1855-1857. DOI: 10.1016/S0031-9422(00)81715-X |
0.619 |
|
| 1987 |
COREY EJ, REID JG, MYERS AG, HAHL RW. ChemInform Abstract: Simple Synthetic Route to the Limonoid System. Cheminform. 18. DOI: 10.1002/chin.198724285 |
0.638 |
|
| 1986 |
Corey EJ, Naef R, Hannon FJ. Enantioselective conjugate addition of rationally designed chiral cuprate reagents to 2-cycloalkenones Journal of the American Chemical Society. 108: 7114-7116. DOI: 10.1021/Ja00282A052 |
0.321 |
|
| 1986 |
Corey EJ, Su W, Houpis IN. Useful new annulation reactions of vicinal dicarboxylic esters Tetrahedron Letters. 27: 5951-5954. DOI: 10.1016/S0040-4039(00)85370-8 |
0.426 |
|
| 1986 |
Corey EJ, Mehrotra MM. A stereoselective and practical synthesis of 5,6(S,S)-epoxy-15(S)-hydroxy-7(E),9(E),11(Z),13(E)-eicosatetraenoic acid (4), possible precursor of the lipoxins Tetrahedron Letters. 27: 5173-5176. DOI: 10.1016/S0040-4039(00)85161-8 |
0.343 |
|
| 1986 |
Corey E, Myers AG, Takahashi N, Yamane H, Schraudolf H. Constitution of antheridium-inducing factor of anemia phyllitidis Tetrahedron Letters. 27: 5083-5084. DOI: 10.1016/S0040-4039(00)85138-2 |
0.615 |
|
| 1986 |
Corey EJ, d'Alarcao M. 12-methylidene-10(Z), 13(Z)-nonadecadienoic acid, a new irreversible inhibitor of soybean lipoxygenase Tetrahedron Letters. 27: 3589-3590. DOI: 10.1016/S0040-4039(00)84856-X |
0.692 |
|
| 1986 |
Corey E, d'Alarcao M, Matsuda SP. A new irreversible inhibitor of soybean lipoxygenase; relevance to mechanism Tetrahedron Letters. 27: 3585-3588. DOI: 10.1016/S0040-4039(00)84855-8 |
0.695 |
|
| 1986 |
Corey E, Seibel WL. A simple stereoselective synthesis of -γ-bisabolene Tetrahedron Letters. 27: 909-910. DOI: 10.1016/S0040-4039(00)84134-9 |
0.418 |
|
| 1986 |
Corey E, Seibel WL. First stekeospecific synthesis of -γ-bisabolene. A method for the concurrent generation of a ring and a tetrasubstituted exocyclic double bond. Tetrahedron Letters. 27: 905-908. DOI: 10.1016/S0040-4039(00)84133-7 |
0.392 |
|
| 1986 |
COREY EJ, MYERS AG. ChemInform Abstract: Total Synthesis of (±)-Antheridium-Inducing Factor (A M) of the Fern Anemia phyllitidis. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198601325 |
0.594 |
|
| 1985 |
Lee TH, Mencia-Huerta JM, Shih C, Corey EJ, Lewis RA, Austen KF. Effects of exogenous arachidonic, eicosapentaenoic, and docosahexaenoic acids on the generation of 5-lipoxygenase pathway products by ionophore-activated human neutrophils. The Journal of Clinical Investigation. 74: 1922-33. PMID 6096400 DOI: 10.1172/Jci111612 |
0.31 |
|
| 1985 |
Spadari S, Focher F, Kuenzle C, Corey EJ, Myers AG, Hardt N, Rebuzzini A, Ciarrocchi G, Pedrali-Noy G. In vivo distribution and activity of aphidicolin on dividing and quiescent cells. Antiviral Research. 5: 93-101. PMID 3925878 DOI: 10.1016/0166-3542(85)90035-X |
0.596 |
|
| 1985 |
Corey EJ, Long AK, Rubenstein SD. Computer-assisted analysis in organic synthesis. Science (New York, N.Y.). 228: 408-18. PMID 3838594 DOI: 10.1126/Science.3838594 |
0.345 |
|
| 1985 |
Marfat A, Corey EJ. Synthesis and structure elucidation of leukotrienes. Advances in Prostaglandin, Thromboxane, and Leukotriene Research. 14: 155-228. PMID 2992244 |
0.748 |
|
| 1985 |
Corey EJ, Myers AG. Total synthesis of (.+-.)-antheridium-inducing factor (AAn) of the Fern Anemia phyllitidis. Clarification of stereochemistry Journal of the American Chemical Society. 107: 5574-5576. DOI: 10.1021/Ja00305A067 |
0.661 |
|
| 1985 |
Corey EJ, Desai MC, Engler TA. Total synthesis of (.+-.)-retigeranic acid Cheminform. 16: 4339-4341. DOI: 10.1021/Ja00300A049 |
0.383 |
|
| 1985 |
Corey EJ, Peterson RT. Enantioselective Michael reactions. Stereoselective addition of enolates of phenmenthol esters to crotonates Tetrahedron Letters. 26: 5025-5028. DOI: 10.1016/S0040-4039(01)80843-1 |
0.438 |
|
| 1985 |
Corey EJ, Su W. Simple synthesis and assignment of stereochemistry of lipoxin A Tetrahedron Letters. 26: 281-284. DOI: 10.1016/S0040-4039(01)80797-8 |
0.414 |
|
| 1985 |
Corey EJ, Desai MC. Highly reactive equivalents of allylidenetriphenylphosphoranes for the stereospecific synthesis of 1,3-dienes by cis-olefination of hindered aldehydes Tetrahedron Letters. 26: 5747-5748. DOI: 10.1016/S0040-4039(00)98914-7 |
0.404 |
|
| 1985 |
Corey EJ, Gross AW. Carbolactonization of olefins under mild conditions by cyanoacetic and malonic acids promoted by manganese (III) acetate Tetrahedron Letters. 26: 4291-4294. DOI: 10.1016/S0040-4039(00)98715-X |
0.325 |
|
| 1985 |
Corey EJ, d'Alarcao M, Kyler KS. Synthesis of new lipoxygenase inhibitors 13-thia- and 10-thiaarachidonic acids Tetrahedron Letters. 26: 3919-3922. DOI: 10.1016/S0040-4039(00)98687-8 |
0.716 |
|
| 1985 |
Corey EJ, Mehrotra MM, Su W. On the synthesis and structure of lipoxin B Tetrahedron Letters. 26: 1919-1922. DOI: 10.1016/S0040-4039(00)98341-2 |
0.347 |
|
| 1985 |
Corey EJ, Boaz NW. The reactions of combined organocuprate-chlorotrimethylsilane reagents with conjugated carbonyl compounds Tetrahedron Letters. 26: 6019-6022. DOI: 10.1016/S0040-4039(00)95114-1 |
0.662 |
|
| 1985 |
Corey EJ, Boaz NW. Evidence for a reversible d, π-complexation, β-cupration sequence in the conjugate addition reaction of Gilman reagents with α,β-enones. Tetrahedron Letters. 26: 6015-6018. DOI: 10.1016/S0040-4039(00)95113-X |
0.656 |
|
| 1985 |
Corey EJ, Desai MC. Simple synthesis of (±)-β-trans-bergamotene Tetrahedron Letters. 26: 3535-3538. DOI: 10.1016/S0040-4039(00)89184-4 |
0.311 |
|
| 1985 |
Corey EJ, Kang J, Kyler K. Activation of methylenetriphenylphosphorane by reaction with t-butyl- or sec-butyllithium Tetrahedron Letters. 26: 555-558. DOI: 10.1016/S0040-4039(00)89146-7 |
0.302 |
|
| 1985 |
Corey EJ, Gross AW. Methods for the synthesis of chiral hindered amines The Journal of Organic Chemistry. 50: 5391-5393. DOI: 10.1002/Chin.198623170 |
0.405 |
|
| 1985 |
Corey EJ, Samuelsson B. One-Step Conversion Of Primary Alcohols In The Carbohydrate Series To The Corresponding Carboxylic Tert-Butyl Esters Cheminform. 16. DOI: 10.1002/Chin.198521334 |
0.513 |
|
| 1985 |
Corey EJ, Dittami JP. Total Synthesis Of (.+-.)-Ovalicin Cheminform. 16. DOI: 10.1002/Chin.198519311 |
0.421 |
|
| 1985 |
COREY EJ, CLARK DA, MARFAT A. ChemInform Abstract: STRUCTURE ELUCIDATION AND TOTAL SYNTHESIS OF THE LEUKOTRIENES Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198510383 |
0.771 |
|
| 1985 |
Corey EJ, Shimoji K, Shih C. Synthesis Of Prostaglandins Via A 1,2-Dioxabicyclo(2.2.1)Heptane (Endoperoxide) Intermediate. Stereochemical Divergence Of Enzymic And Biomimetic Chemical Cyclization Reactions Cheminform. 16. DOI: 10.1002/Chin.198506191 |
0.367 |
|
| 1984 |
Corey EJ, Samuelsson B. One-step conversion of primary alcohols in the carbohydrate series to the corresponding carboxylic tert-butyl esters Journal of Organic Chemistry. 49: 4735-4735. DOI: 10.1021/Jo00198A034 |
0.513 |
|
| 1984 |
Corey EJ, Shimoji K, Shih C. Synthesis of prostaglandins via a 1,2-dioxabicyclo[2.2.1]heptane (endoperoxide) intermediate. Stereochemical divergence of enzymic and biomimetic chemical cyclization reactions Journal of the American Chemical Society. 106: 6425-6427. DOI: 10.1021/Ja00333A057 |
0.366 |
|
| 1984 |
Corey EJ, Samuelsson B, Luzzio FA. A new method for the synthesis of organic nitro compounds Journal of the American Chemical Society. 106: 3682-3683. DOI: 10.1021/Ja00324A052 |
0.523 |
|
| 1984 |
Corey EJ, De B. Total synthesis and stereochemistry of hybridalactone Journal of the American Chemical Society. 106: 2735-2736. DOI: 10.1021/Ja00321A063 |
0.43 |
|
| 1984 |
Corey EJ, Tramontano A. Total synthesis of bongkrekic acid Journal of the American Chemical Society. 106: 462-463. DOI: 10.1021/Ja00314A056 |
0.383 |
|
| 1984 |
Corey EJ, Hua DH, Seitz SP. Methods for the interconversion of protective groups. Transformation of mem ethers into isopropylthiomethyl ethers or cyanomethyl ethers Tetrahedron Letters. 25: 3-6. DOI: 10.1016/S0040-4039(01)91133-5 |
0.376 |
|
| 1984 |
Corey E, Myers AG. Efficient synthesis and intramolecular cyclopropanation of unsaturated diazoacetic esters Tetrahedron Letters. 25: 3559-3562. DOI: 10.1016/S0040-4039(01)91075-5 |
0.691 |
|
| 1984 |
Corey EJ, Su W, Mehrotra MM. An efficient and simple method for the conversion of 15-HPETE to 14,15-EPETE (lipotriene A) and 5-HPETE to leukotriene a as the methyl esters Tetrahedron Letters. 25: 5123-5126. DOI: 10.1016/S0040-4039(01)81540-9 |
0.364 |
|
| 1984 |
Corey EJ, Su W. Total synthesis of biologically active metabolites of arachidonic acid. The two 8-hydroxy-11,12(S,S)-epoxyeicosa-5,14(Z),9(E)-trienoic acids. Tetrahedron Letters. 25: 5119-5122. DOI: 10.1016/S0040-4039(01)81539-2 |
0.393 |
|
| 1984 |
Corey EJ, Kyler K, Raju N. A short,three-component total synthesis of 12-hydroxyeicosa-5,8,14(Z), 10(E)-tetraenoic acid (12-HETE) via the corresponding ketone Tetrahedron Letters. 25: 5115-5118. DOI: 10.1016/S0040-4039(01)81538-0 |
0.388 |
|
| 1984 |
Corey E, Rücker C. The 1,3 O→C silyl rearrangement of silyl enol ether anions - synthesis of α-silyl ketones Tetrahedron Letters. 25: 4345-4348. DOI: 10.1016/S0040-4039(01)81434-9 |
0.364 |
|
| 1984 |
Corey E, Ponder JW. Stereochemistry of the hygrolidins Tetrahedron Letters. 25: 4325-4328. DOI: 10.1016/S0040-4039(01)81429-5 |
0.612 |
|
| 1984 |
Corey EJ, Wright SW. A Simple Process For The Purification Of Arachidonic Acid Tetrahedron Letters. 25: 2729-2730. DOI: 10.1016/S0040-4039(01)81275-2 |
0.307 |
|
| 1984 |
Corey EJ, Wright SW. A Convenient Synthesis Of O-Alkyl Thioesters From Esters Tetrahedron Letters. 25: 2639-2640. DOI: 10.1016/S0040-4039(01)81250-8 |
0.335 |
|
| 1984 |
Corey E, Eckrich TM. A new route to -disubstituted olefins. A simple synthesis of polyunsaturated fatty acids by reiterative coupling Tetrahedron Letters. 25: 2419-2422. DOI: 10.1016/S0040-4039(01)81194-1 |
0.365 |
|
| 1984 |
Corey E, Eckrich TM. A method for the stereospecific synthesis of chiral -2-alkylcyclopropyllithium reagents Tetrahedron Letters. 25: 2415-2418. DOI: 10.1016/S0040-4039(01)81193-X |
0.379 |
|
| 1984 |
Corey E, De B, Ponder JW, Berg JM. The stereochemistry and biosynthesis of hybridalactone, an eicosanoid from Tetrahedron Letters. 25: 1015-1018. DOI: 10.1016/S0040-4039(01)80088-5 |
0.618 |
|
| 1984 |
Corey EJ, Gross AW. Highly selective, kinetically controlled enolate formation using lithium dialkylamides in the presence of trimethylchlorosilane Tetrahedron Letters. 25: 495-498. DOI: 10.1016/S0040-4039(00)99920-9 |
0.303 |
|
| 1984 |
Corey E, Engler T. Methods for stereospecific synthesis of or hydrindanones Tetrahedron Letters. 25: 149-152. DOI: 10.1016/S0040-4039(00)99826-5 |
0.336 |
|
| 1984 |
Corey EJ, Boaz NW. d-orbital stereoelectronic control of the stereochemistry of SN2′ displacements by organocuprate reagents Tetrahedron Letters. 25: 3063-3066. DOI: 10.1016/0040-4039(84)80008-8 |
0.644 |
|
| 1984 |
Corey EJ, Boaz NW. Stereochemistry of the sn2′ displacement of chiral 1, 3-disubstituted bromoallenes to form chiral acetylenes Tetrahedron Letters. 25: 3059-3062. DOI: 10.1016/0040-4039(84)80007-6 |
0.668 |
|
| 1984 |
Corey EJ, Boaz NW. A stereospecific synthesis of chiral 1,3-disubstituted bromoallenes Tetrahedron Letters. 25: 3055-3058. DOI: 10.1016/0040-4039(84)80006-4 |
0.656 |
|
| 1984 |
Corey EJ, Ohuchida S, Hahl R. Total synthesis of C22-prostanoids in the E and F series based on docosahexaenoic acid Journal of the American Chemical Society. 106: 3875-3876. DOI: 10.1002/Chin.198440335 |
0.327 |
|
| 1984 |
Corey EJ, Samuelsson B, Luzzio FA. A New Method For The Synthesis Of Organic Nitro Compounds Cheminform. 15. DOI: 10.1002/Chin.198439296 |
0.523 |
|
| 1984 |
Corey EJ, Mehrotra MM. Total synthesis of (.+-.)-clavulones Journal of the American Chemical Society. 106: 3384-3384. DOI: 10.1002/Chin.198436332 |
0.418 |
|
| 1984 |
Corey EJ, De B. Total Synthesis And Stereochemistry Of Hybridalactone Cheminform. 15. DOI: 10.1002/Chin.198432329 |
0.433 |
|
| 1984 |
Corey EJ, Tramontano A. Total Synthesis Of Bongkrekic Acid Cheminform. 15. DOI: 10.1002/Chin.198417373 |
0.403 |
|
| 1983 |
Corey EJ, Shih C, Cashman JR. Docosahexaenoic acid is a strong inhibitor of prostaglandin but not leukotriene biosynthesis. Proceedings of the National Academy of Sciences of the United States of America. 80: 3581-4. PMID 6304720 DOI: 10.1073/Pnas.80.12.3581 |
0.315 |
|
| 1983 |
Corey EJ. Chemical studies on slow reacting substances/leukotrienes. Experientia. 38: 1259-75. PMID 6129158 DOI: 10.1007/Bf01954913 |
0.328 |
|
| 1983 |
Corey EJ, Albright JO. Total synthesis of leukotrienes. An effective procedure for the synthesis of conjugated dienals by four-carbon homologation Journal of Organic Chemistry. 48: 2114-2115. DOI: 10.1021/Jo00160A042 |
0.367 |
|
| 1983 |
Corey EJ, Shimoji K. Total synthesis of the major human urinary metabolite of prostaglandin D2, a key diagnostic indicator Journal of the American Chemical Society. 105: 1662-1664. DOI: 10.1021/Ja00344A047 |
0.306 |
|
| 1983 |
Corey EJ, Mehrotra MM. Stereochemistry of the lipoxygenase-catalyzed allylic hydroperoxide→oxiranylcarbinol rearrangements Tetrahedron Letters. 24: 4921-4922. DOI: 10.1016/S0040-4039(01)99811-9 |
0.302 |
|
| 1983 |
Corey E, Mehrotra MM, Cashman JR. New synthetic routes to leukotrienes and other arachidonate derived epoxy eicosatetraenoic acids (epete's). Exclusion of the hydroxy epoxide pathway for leukotriene biosynthesis Tetrahedron Letters. 24: 4917-4920. DOI: 10.1016/S0040-4039(01)99810-7 |
0.413 |
|
| 1983 |
Corey E, Kang J, Laguzza BC, Jones RL. Total synthesis of 12-()-10-hydroxy--11,12-epoxyeicosa-5,9,14-()-trienoic acids, metabolites of arachidonic acid in mammalian blood platelets Tetrahedron Letters. 24: 4913-4916. DOI: 10.1016/S0040-4039(01)99809-0 |
0.318 |
|
| 1983 |
Corey EJ, Pyne SG, Su W. Total Synthesis Of Leukotriene B5 Tetrahedron Letters. 24: 4883-4886. DOI: 10.1016/S0040-4039(01)99801-6 |
0.342 |
|
| 1983 |
Corey EJ, Raju N. A new general synthetic route to bridged carboxylic ortho esters Tetrahedron Letters. 24: 5571-5574. DOI: 10.1016/S0040-4039(00)94143-1 |
0.394 |
|
| 1983 |
Corey E, Eckrich TM. A new and simple synthesis of alkoxy- and aryloxymethyllithium reagents (roch2li) Tetrahedron Letters. 24: 3163-3164. DOI: 10.1016/S0040-4039(00)88124-1 |
0.375 |
|
| 1983 |
Corey EJ, Pyne SG. Conversion of ketones having δ, ε{lunate}-π-functions to cyclopentanols by zinc-trimethylchlorosilane Tetrahedron Letters. 24: 2821-2824. DOI: 10.1016/S0040-4039(00)88033-8 |
0.323 |
|
| 1983 |
Corey EJ, Pyne SG, Schafer AI. Synthesis of a new series of potent inhibitors of thromboxane A2 biosynthesis Tetrahedron Letters. 24: 3291-3294. DOI: 10.1016/S0040-4039(00)86251-6 |
0.303 |
|
| 1983 |
Corey E, Shimoji K. Magnesium and zinc-catalyzed thioketalization Tetrahedron Letters. 24: 169-172. DOI: 10.1016/S0040-4039(00)81357-X |
0.347 |
|
| 1983 |
Corey EJ, Iguchi S, Albright JO, De B. Studies on the conformational mobility of arachidonic acid. Facile macrolactonization of 20-hydroxyarachidonic acid. Tetrahedron Letters. 24: 37-40. DOI: 10.1016/S0040-4039(00)81320-9 |
0.304 |
|
| 1983 |
Corey EJ, Albright JO. Total synthesis of leukotrienes. An effective procedure for the synthesis of conjugated dienals by four-carbon homologation Cheminform. 14. DOI: 10.1002/Chin.198346347 |
0.367 |
|
| 1983 |
Corey EJ, Pan BC, Hua DH, Deardorff DR. Total synthesis of aplasmomycin. Stereocontrolled construction of the C(3)-C(17) fragment Cheminform. 14. DOI: 10.1002/Chin.198309339 |
0.31 |
|
| 1982 |
Lee CW, Lewis RA, Corey EJ, Barton A, Oh H, Tauber AI, Austen KF. Oxidative inactivation of leukotriene C4 by stimulated human polymorphonuclear leukocytes. Proceedings of the National Academy of Sciences of the United States of America. 79: 4166-70. PMID 6955794 DOI: 10.1073/Pnas.79.13.4166 |
0.463 |
|
| 1982 |
Lewis RA, Mencia-Huerta JM, Soberman RJ, Hoover D, Marfat A, Corey EJ, Austen KF. Radioimmunoassay for leukotriene B4. Proceedings of the National Academy of Sciences of the United States of America. 79: 7904-8. PMID 6296855 DOI: 10.1073/Pnas.79.24.7904 |
0.733 |
|
| 1982 |
Showell HJ, Otterness IG, Marfat A, Corey EJ. Inhibition of leukotriene B4-induced neutrophil degranulation by leukotriene B4-dimethylamide. Biochemical and Biophysical Research Communications. 106: 741-7. PMID 6288032 DOI: 10.1016/0006-291X(82)91773-9 |
0.723 |
|
| 1982 |
Drazen JM, Venugopalan CS, Austen KF, Brion F, Corey EJ. Effects of leukotriene E on pulmonary mechanics in the guinea pig. The American Review of Respiratory Disease. 125: 290-4. PMID 6279000 DOI: 10.1164/Arrd.1982.125.3.290 |
0.503 |
|
| 1982 |
Corey EJ, Hua DH, Pan BC, Seitz SP. Total synthesis of aplasmomycin Journal of the American Chemical Society. 104: 6818-6820. DOI: 10.1021/Ja00388A074 |
0.421 |
|
| 1982 |
Corey EJ, Pan BC, Hua DH, Deardorff DR. Total synthesis of aplasmomycin. Stereocontrolled construction of the C(3)-C(17) fragment Journal of the American Chemical Society. 104: 6816-6818. DOI: 10.1021/Ja00388A073 |
0.31 |
|
| 1982 |
Corey EJ, Munroe JE. Total synthesis of gibberellic acid. A simple synthesis of a key intermediate Journal of the American Chemical Society. 104: 6129-6130. DOI: 10.1021/Ja00386A055 |
0.438 |
|
| 1982 |
Corey EJ, Hoover DJ. Total synthesis of 5-desoxyleukotriene D. A new and useful equivalent of the 4-formyl-trans, trans-1,3-butadienyl anion Tetrahedron Letters. 23: 3463-3466. DOI: 10.1016/S0040-4039(00)87642-X |
0.38 |
|
| 1982 |
Corey E, Barton AE. Chemical conversion of arachidonic acid to slow reacting substances Tetrahedron Letters. 23: 2351-2354. DOI: 10.1016/S0040-4039(00)87339-6 |
0.355 |
|
| 1982 |
Corey EJ, Hopkins B. A mild procedure for the conversion of 1,2-diols to olefins Tetrahedron Letters. 23: 1979-1982. DOI: 10.1016/S0040-4039(00)87238-X |
0.356 |
|
| 1982 |
Corey E, Kang J. Short, stereocontrolled syntheses of irreversible eicosanoid biosynthesis inhibitors. 5,6- , 8,9- , and 11,12-dehydroarachidonic acid Tetrahedron Letters. 23: 1651-1654. DOI: 10.1016/S0040-4039(00)87181-6 |
0.353 |
|
| 1982 |
Corey E, Rücker C. Useful synthetic reagents derived from 1-triisopropylsilylpropyne and 1,3-[triisopropylsilyl]propyne, direct, stereoselective synthesis of either or enynes Tetrahedron Letters. 23: 719-722. DOI: 10.1016/S0040-4039(00)86930-0 |
0.41 |
|
| 1982 |
Corey EJ, Hopkins PB. Diisopropylsilyl ditriflate and di-tert-butysilyl ditriflate: new reagents for the protection of diols Tetrahedron Letters. 23: 4871-4874. DOI: 10.1016/S0040-4039(00)85735-4 |
0.647 |
|
| 1982 |
Corey EJ, Hopkins PB, Barton AE, Bangerter B, Borgeat P. Proton magnetic resonance spectra of leukotriene a methyl ester (I), leukotriene B methyl ester diacetate (II) and 12-epi-6-E,8-Z-leukotriene B methyl ester diacetate (III; 5-S,12-di-HETE) Tetrahedron. 38: 2653-2657. DOI: 10.1016/0040-4020(82)80018-5 |
0.586 |
|
| 1982 |
Corey EJ, Hoover DJ. Total Synthesis Of 5‐Desoxyleukotriene D. A New And Useful Equivalent Of The 4‐Formyl‐Trans,Trans‐1,3‐Butadienyl Anion Cheminform. 14: 3463-3466. DOI: 10.1002/Chin.198301362 |
0.376 |
|
| 1981 |
Levine L, Morgan RA, Lewis RA, Austen KF, Clark DA, Marfat A, Corey EJ. Radioimmunoassay of the leukotrienes of slow reacting substance of anaphylaxis. Proceedings of the National Academy of Sciences of the United States of America. 78: 7692-6. PMID 6950409 DOI: 10.1073/Pnas.78.12.7692 |
0.731 |
|
| 1981 |
Baskar JF, Torchiana DF, Biggers JD, Corey EJ, Andersen NH, Subramanian N. Inhibition of hatching of mouse blastocysts in vitro by various prostaglandin antagonists. Journal of Reproduction and Fertility. 63: 359-63. PMID 6946238 DOI: 10.1530/Jrf.0.0630359 |
0.481 |
|
| 1981 |
Drazen JM, Lewis RA, Austen KF, Toda M, Brion F, Marfat A, Corey EJ. Contractile activities of structural analogs of leukotrienes C and D: necessity of a hydrophobic region. Proceedings of the National Academy of Sciences of the United States of America. 78: 3195-8. PMID 6942424 DOI: 10.1073/Pnas.78.5.3195 |
0.776 |
|
| 1981 |
Lewis RA, Drazen JM, Austen KF, Toda M, Brion F, Marfat A, Corey EJ. Contractile activities of structural analogs of leukotrienes C and D: role of the polar substituents. Proceedings of the National Academy of Sciences of the United States of America. 78: 4579-83. PMID 6270684 DOI: 10.1073/Pnas.78.7.4579 |
0.772 |
|
| 1981 |
Corey EJ, Kang J. Stereospecific total synthesis of 11(R)-HETE (2), lipoxygenation product of arachidonic acid via the prostaglandin pathway Journal of the American Chemical Society. 103: 4618-4619. DOI: 10.1021/Ja00405A071 |
0.333 |
|
| 1981 |
Corey EJ, Hashimoto S, Barton AE. Chirally directed synthesis of (-)-methyl 5(S), 6(S)-oxido-7-hydroxyheptanoate, a key intermediate for the total synthesis of leukotrienes A, C, D and E Journal of the American Chemical Society. 103: 721-722. DOI: 10.1021/Ja00393A063 |
0.38 |
|
| 1981 |
Corey EJ, Estreicher H. 3-Nitrocycloalkenones, synthesis and use as reverse affinity cycloalkynone equivalents Tetrahedron Letters. 22: 603-606. DOI: 10.1016/S0040-4039(01)92500-6 |
0.391 |
|
| 1981 |
Corey EJ, Marfat A, Hoover DJ. Stereospecific total synthesis of 12-(r)- and 12- (s)-forms of 6-trans leukotriene B Tetrahedron Letters. 22: 1587-1590. DOI: 10.1016/S0040-4039(01)90384-3 |
0.759 |
|
| 1981 |
Corey EJ, Marfat A, Munroe J, Kim KS, Hopkins PB, Brion F. A Stereocontrolled and effective synthesis of leukotriene B (1). Tetrahedron Letters. 22: 1077-1080. DOI: 10.1016/S0040-4039(01)90241-2 |
0.795 |
|
| 1981 |
Corey E, Cho H, Rücker C, Hua DH. Studies with trialkylsilyltriflates: new syntheses and applications Tetrahedron Letters. 22: 3455-3458. DOI: 10.1016/S0040-4039(01)81930-4 |
0.339 |
|
| 1981 |
Corey EJ, Marfat A, Laguzza BC. Total synthesis of 5S, 12S-dihydroxy-6,10-E,8,14-Z-eicosatetraenoic acid (5S,12S-di-HETE) (2), a new human metabolite of arachidonic acid Tetrahedron Letters. 22: 3339-3342. DOI: 10.1016/S0040-4039(01)81899-2 |
0.765 |
|
| 1981 |
Corey E, Hashimoto S. A practical process for large-scale synthesis of (S)-5-hydroxy-6-trans-8,11,14-cis-eicosatetraenoic acid (5-HETE) Tetrahedron Letters. 22: 299-302. DOI: 10.1016/0040-4039(81)80080-9 |
0.369 |
|
| 1981 |
COREY EJ, HOPKINS PB, MUNROE JE, MARFAT A, HASHIMOTO S. ChemInform Abstract: TOTAL SYNTHESIS OF 6-TRANS,10-CIS AND (.+-.)-6-TRANS,8-CIS ISOMERS OF LEUKOTRIENE B Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198114329 |
0.781 |
|
| 1981 |
COREY EJ, WEIGEL LO, CHAMBERLIN AR, CHO H, HUA DH. ChemInform Abstract: TOTAL SYNTHESIS OF MAYTANSINE Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198103312 |
0.648 |
|
| 1980 |
Corey EJ, Niwa H, Falck JR, Mioskowski C, Arai Y, Marfat A. Recent studies on the chemical synthesis of eicosanoids. Advances in Prostaglandin and Thromboxane Research. 6: 19-25. PMID 7386258 |
0.786 |
|
| 1980 |
Drazen JM, Austen KF, Lewis RA, Clark DA, Goto G, Marfat A, Corey EJ. Comparative airway and vascular activities of leukotrienes C-1 and D in vivo and in vitro. Proceedings of the National Academy of Sciences of the United States of America. 77: 4354-8. PMID 6933488 DOI: 10.1073/Pnas.77.7.4354 |
0.721 |
|
| 1980 |
Clark DA, Goto G, Marfat A, Corey EJ, Hammarström S, Samuelsson B. 11-Trans leukotriene C: a naturally occurring slow reacting substance. Biochemical and Biophysical Research Communications. 94: 1133-9. PMID 6772184 DOI: 10.1016/0006-291X(80)90537-9 |
0.79 |
|
| 1980 |
Rådmark O, Malmsten C, Samuelsson B, Goto G, Marfat A, Corey EJ. Leukotriene A. Isolation from human polymorphonuclear leukocytes. The Journal of Biological Chemistry. 255: 11828-31. PMID 6254983 |
0.735 |
|
| 1980 |
Lewis RA, Drazen JM, Austen KF, Clark DA, Corey EJ. Identification of the C(6)-S-conjugate of leukotriene A with cysteine as a naturally occurring slow reacting substance of anaphylaxis (SRS-A). Importance of the 11-cis-geometry for biological activity. Biochemical and Biophysical Research Communications. 96: 271-7. PMID 6254506 DOI: 10.1016/0006-291X(80)91210-3 |
0.301 |
|
| 1980 |
Rådmark O, Malmsten C, Samuelsson B, Clark DA, Goto G, Marfat A, Corey EJ. Leukotriene A: stereochemistry and enzymatic conversion to leukotriene B. Biochemical and Biophysical Research Communications. 92: 954-61. PMID 6244821 DOI: 10.1016/0006-291X(80)90795-0 |
0.789 |
|
| 1980 |
Lewis RA, Austen KF, Drazen JM, Clark DA, Marfat A, Corey EJ. Slow reacting substances of anaphylaxis: identification of leukotrienes C-1 and D from human and rat sources. Proceedings of the National Academy of Sciences of the United States of America. 77: 3710-4. PMID 6106193 DOI: 10.1073/Pnas.77.6.3710 |
0.728 |
|
| 1980 |
Hammarström S, Samuelsson B, Clark DA, Goto G, Marfat A, Mioskowski C, Corey EJ. Stereochemistry of leukotriene C-1. Biochemical and Biophysical Research Communications. 92: 946-53. PMID 6102463 DOI: 10.1016/0006-291X(80)90794-9 |
0.783 |
|
| 1980 |
Schomburg D, Hopkins PB, Lipscomb WN, Corey EJ. Total synthesis of erythromycins. 6. Facile transformation of erythronolide A into a tricyclic internal ketal Cheminform. 11: 1544-1546. DOI: 10.1021/Jo01296A051 |
0.615 |
|
| 1980 |
Corey E, Hopkins P, Munroe J, Marfat A, Hashimoto S. Total Synthesis of 6-Trans, 10-cis and (plus or minus) -6-Trans,8-cis Isomers of Leukotriene B Journal of the American Chemical Society. 102: 7986-7987. DOI: 10.1021/Ja00547A600 |
0.779 |
|
| 1980 |
Corey EJ, Marfat A, Goto G, Brion F. Leukotriene B. Total synthesis and assignment of stereochemistry Journal of the American Chemical Society. 102: 7984-7985. DOI: 10.1021/Ja00547A051 |
0.795 |
|
| 1980 |
Corey EJ, Tius MA, Das J. Total synthesis of (.+-.)-stemodin and (.+-.)-stemodinone Journal of the American Chemical Society. 102: 7612-7613. DOI: 10.1021/Ja00545A060 |
0.631 |
|
| 1980 |
Corey EJ, Weigel LO, Chamberlin AR, Cho H, Hua DH. Total synthesis of maytansine Journal of the American Chemical Society. 102: 6613-6615. DOI: 10.1021/Ja00541A064 |
0.644 |
|
| 1980 |
Corey EJ, Goto G, Marfat A. Simple synthesis of the 11,12-oxido and 14,15-oxido analogs of leukotriene A and the corresponding conjugates with glutathione and cysteinylglycine, analogs of leukotrienes C and D Journal of the American Chemical Society. 102: 6607-6608. DOI: 10.1021/Ja00541A060 |
0.76 |
|
| 1980 |
Corey EJ, Barton AE, Clark DA. Synthesis of the slow reacting substance of anaphylaxis leukotriene C-1 from arachidonic acid Journal of the American Chemical Society. 102: 4278-4279. DOI: 10.1021/Ja00532A059 |
0.369 |
|
| 1980 |
Corey E, Clark D, Goto G, Marfat A, Mioskowski C, Samuelsson B, Hammarstrom S. Additions and Corrections - Stereospecific Total Synthesis of a "Slow Reacting Substance" of Anaphylaxis Leukotriene C-1 Journal of the American Chemical Society. 102: 3663-3663. DOI: 10.1021/Ja00530A611 |
0.787 |
|
| 1980 |
Corey EJ, Tius MA, Das J. Total synthesis of (.+-.)-aphidicolin Journal of the American Chemical Society. 102: 1742-1744. DOI: 10.1021/Ja00525A055 |
0.63 |
|
| 1980 |
Corey EJ, Clark DA, Goto G, Marfat A, Mioskowski C, Samuelsson B, Hammarstroem S. Stereospecific total synthesis of a "slow reacting substance" of anaphylaxis, leukotriene C-1 Journal of the American Chemical Society. 102: 1436-1439. DOI: 10.1021/Ja00524A045 |
0.796 |
|
| 1980 |
Corey EJ, Marfat A, Falck JR, Albright JO. Controlled chemical synthesis of the enzymatically produced eicosanoids 11-, 12-, and 15-HETE from arachidonic acid and conversion into the corresponding hydroperoxides(HPETE) [13] Journal of the American Chemical Society. 102: 1433-1435. DOI: 10.1021/Ja00524A043 |
0.769 |
|
| 1980 |
Corey EJ, Estreicher H. An effective and mild method for the conversion of oximes to secondary nitro compounds Tetrahedron Letters. 21: 1117-1120. DOI: 10.1016/S0040-4039(01)83928-9 |
0.315 |
|
| 1980 |
Corey EJ, Estreicher H. Nitrodestannylation. A new synthesis of conjugated nitro cyclo olefins Tetrahedron Letters. 21: 1113-1116. DOI: 10.1016/S0040-4039(01)83927-7 |
0.398 |
|
| 1980 |
Corey EJ, Park H, Barton A, Nii Y. Synthesis of three potential inhibitors of the biosynthesis of leukotrienes A–E Tetrahedron Letters. 21: 4243-4246. DOI: 10.1016/S0040-4039(00)92873-9 |
0.535 |
|
| 1980 |
Corey EJ, Pearce HL. Total synthesis of picrotin Tetrahedron Letters. 21: 1823-1824. DOI: 10.1016/S0040-4039(00)92789-8 |
0.813 |
|
| 1980 |
Corey EJ, Gross AW. Bislactonization of unsaturated diacids using lead tetraacetate Tetrahedron Letters. 21: 1819-1822. DOI: 10.1016/S0040-4039(00)92788-6 |
0.354 |
|
| 1980 |
Corey E, Goto G. Total synthesis of slow reacting substances (SRS's): 6--leukotriene C and 6--leukotriene D Tetrahedron Letters. 21: 3463-3466. DOI: 10.1016/S0040-4039(00)78715-6 |
0.304 |
|
| 1980 |
Corey EJ, Clark DA, Marfat A, Goto G. Total synthesis of slow reacting substances (SRS). "Leukotriene C-2" (11-trans-leukotriene C) (3) and leukotriene D (4) Tetrahedron Letters. 21: 3143-3146. DOI: 10.1016/S0040-4039(00)77430-2 |
0.749 |
|
| 1980 |
Corey EJ, Clark DA. Studies on the total synthesis of rifamycin. A method for the closure of the macrocyclic unit Tetrahedron Letters. 21: 2045-2048. DOI: 10.1016/S0040-4039(00)71481-X |
0.4 |
|
| 1980 |
Corey E, Ponder JW, Ulrich P. Synthesis of a stable analog of thromboxane A2 with methylene replacing the 9,11-bridging oxygen Tetrahedron Letters. 21: 137-140. DOI: 10.1016/S0040-4039(00)71395-5 |
0.618 |
|
| 1980 |
Corey EJ, Clark DA. Synthesis of two position isomers of leukotriene C having the S-peptide at C(12) Tetrahedron Letters. 21: 3547-3548. DOI: 10.1016/0040-4039(80)80231-0 |
0.311 |
|
| 1980 |
Corey E, Tius MA. 1-diphenylphosphonio-1-methoxymethyllithium, a useful reagent for the synthesis of aldehydes from hindered ketones Tetrahedron Letters. 21: 3535-3538. DOI: 10.1016/0040-4039(80)80227-9 |
0.623 |
|
| 1980 |
Corey EJ, Marfat A, Falck JR, Albright JO. Controlled Chemical Synthesis Of The Enzymically Produced Eicosanoids 11-, 12-, And 15-Hete From Arachidonic Acid And Conversion Into The Corresponding Hydroperoxides (Hpete) Cheminform. 11. DOI: 10.1002/Chin.198021153 |
0.759 |
|
| 1980 |
Corey EJ, Hopkins PB, Kim S, Yoo S, Nambiar KP, Falck JR. Total Synthesis Of Erythromycins. 5. Total Synthesis Of Erythronolide A Cheminform. 11. DOI: 10.1002/Chin.198007355 |
0.421 |
|
| 1979 |
Hammarström S, Murphy RC, Samuelsson B, Clark DA, Mioskowski C, Corey EJ. Structure of leukotriene C. Identification of the amino acid part. Biochemical and Biophysical Research Communications. 91: 1266-72. PMID 43155 DOI: 10.1016/0006-291X(79)91203-8 |
0.526 |
|
| 1979 |
Corey EJ, Hopkins PB, Kim S, Yoo SE, Nambiar KP, Falck JR. Total synthesis of erythromycins. 5. Total synthesis of erythronolide A [41] Journal of the American Chemical Society. 101: 7131-7134. DOI: 10.1021/Ja00517A088 |
0.418 |
|
| 1979 |
Corey EJ, Arai Y, Mioskowski C. Total synthesis of (.+-.)-5,6-oxido-7,9-trans,11,14-cis-eicosapentaenoic acid, a possible precursor of SRSA Journal of the American Chemical Society. 101: 6748-6749. DOI: 10.1021/Ja00516A045 |
0.354 |
|
| 1979 |
Corey EJ, Pearce HL. Total synthesis of picrotoxinin Journal of the American Chemical Society. 101: 5841-5843. DOI: 10.1021/Ja00513A071 |
0.813 |
|
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