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Corey, E.J. Library of Congress/NACO National Library of Israel National Library of Catalonia NII (Japan) BIBSYS

Corey, Elias James, 1928-.... NUKAT Center of Warsaw University Library National Library of the Czech Republic Sudoc [ABES], France National and University Library in Zagreb

Elias James Corey Wikidata

Corey, Elias James National Library of Sweden RERO - Library Network of Western Switzerland National Library of France

Elias James Corey American chemist ISNI

Corey, E. J., 1928- National Library of Estonia German National Library

Corey, E.J. (Elias James), 1928- National Library of the Netherlands

Corey, E. J. (Elias James) National Library of Latvia

VIAF ID: 66530295 (Personal)

Permalink: http://viaf.org/viaf/66530295

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The application of a mechanistic model leads to the extension of the Sharpless asymmetric dihydroxylation to allylic 4-methoxybenzoates and conformationally related amine and homoallylic alcohol derivatives Wikidata
Classics in total synthesis. National Library of Sweden NUKAT Center of Warsaw University Library National Library of the Czech Republic Wikidata National Library of France National Library of Catalonia BIBSYS Sudoc [ABES], France
Computers, the new test tube of chemists [SR] 1981?: Library of Congress/NACO National Library of Israel
Dimethylsulfoxonium Methylide Wikidata
Drug discovery practices, processes, and perspectives Library of Congress/NACO BIBSYS
Efficient and mild lactonization method for the synthesis of macrolides Wikidata
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 Wikidata
Experimental test of the [3+2]- and [2+2]-cycloaddition pathways for the bis-cinchona alkaloid-OsO4 catalyzed dihydroxylation of olefins by means of kinetic isotope effects Wikidata
Facile air oxidation of the conjugate base of rofecoxib (Vioxx™), a possible contributor to chronic human toxicity Wikidata
First application of attractive intramolecular interactions to the design of chiral catalysts for highly enantioselective Diels-Alder reactions Wikidata
General methods for the construction of complex molecules Wikidata
Generation and synthetic applications of 2-lithio-1,3-dithianes Wikidata
Generation of phosphite ylides from trithiocarbonates and trimethyl phosphite and their application to the extension of carbon chains Wikidata
Herstellung und synthetische Verwendung von metallierten Dimethylhydrazonen Regio- und stereoselektive Alkylierung von Carbonylverbindungen Wikidata
Highly enantioselective and diastereoselective Ireland-Claisen rearrangement of achiral allylic esters Wikidata
Internal Photoaddtion Reactions of 2-Pyrone and N-Methyl-2-pyridone: A New Synthetic Approach to Cyclobutadiene Wikidata
The logic of chemical synthesis Library of Congress/NACO National Library of the Netherlands National Library of Latvia Sudoc [ABES], France NII (Japan) National Library of Sweden NUKAT Center of Warsaw University Library RERO - Library Network of Western Switzerland National Library of France National Library of Catalonia BIBSYS Wikidata
Magnesium and zinc-catalyzed thioketalization Wikidata
Methodology for the Preparation of Pure RecombinantS. cerevisiaeLanosterol 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 Wikidata
Molecules and medicine Library of Congress/NACO National Library of the Netherlands NII (Japan) Sudoc [ABES], France NUKAT Center of Warsaw University Library RERO - Library Network of Western Switzerland National Library of Catalonia BIBSYS
Molecules that changed the world : a brief history of the art and science of synthesis and its impact on society National Library of Catalonia BIBSYS NUKAT Center of Warsaw University Library Sudoc [ABES], France
Name reactions for functional group transformations Library of Congress/NACO National Library of the Netherlands Sudoc [ABES], France NUKAT Center of Warsaw University Library National Library of France BIBSYS
Name reactions in heterocyclic chemistry Library of Congress/NACO NUKAT Center of Warsaw University Library National Library of the Netherlands BIBSYS Sudoc [ABES], France
Named reagents, catalysts, and compounds (A-F), 2001?: Library of Congress/NACO National Library of Israel
New enantioselective routes to biologically interesting compounds Wikidata
New general synthetic methods National Library of Sweden
New methods for the oxidation of aldehydes to carboxylic acids and esters Wikidata
New stereospecific synthesis of trisubstituted olefins. Stereospecific synthesis of farnesol Wikidata
Novel electronic effects of remote substituents on the oxazaborolidine-catalyzed enantioselective reduction of ketones Wikidata
Organic synthesis : concepts and methods NUKAT Center of Warsaw University Library Sudoc [ABES], France National Library of France
The origin of greater than 200:1 enantioselectivity in a catalytic Diels-Alder reaction as revealed by physical and chemical studies Wikidata
Oxidative cationic cyclization reactions effected by pyridinium chlorochromate Wikidata
Preparation of an optically active prostaglandin intermediate via asymmetric induction Wikidata
Prostaglandins, a potent future Library of Congress/NACO
Protection of primary hydroxyl groups as methylthiomethyl ethers Wikidata
Pyridinium chlorochromate. An efficient reagent for oxidation of primary and secondary alcohols to carbonyl compounds Wikidata
Reaction of 1,3-dithienium fluoroborate with 1,3-dienes. Synthesis of .DELTA.3-cyclopenten-1-ones Wikidata
Rigid and highly enantioselective catalyst for the dihydroxylation of olefins using osmium tetraoxide clarifies the origin of enantiospecificity Wikidata
Robert Robinson Lecture. Retrosynthetic thinking—essentials and examples Wikidata
Selective formation of carbon-carbon bonds between unlike groups using organocopper reagents Wikidata
Short, Enantioselective Total Synthesis of Aflatoxin B2Using an Asymmetric [3+2]-Cycloaddition Step Wikidata
The stereochemistry and biosynthesis of hybridalactone, an eicosanoid from Wikidata
Stereospecific Syntheses of Olefins from 1,2-Thionocarbonates and 1,2-Trithiocarbonates. trans-Cycloheptene Wikidata
Stereospecific total synthesis of a "slow reacting substance" of anaphylaxis, leukotriene C-1 Wikidata
Strategic applications of named reactions in organic synthesis background and detailed mechanisms National Library of Catalonia NUKAT Center of Warsaw University Library Sudoc [ABES], France National Library of France
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 Wikidata
Studies with trialkylsilyltriflates: new syntheses and applications Wikidata
Synthesewege zu polyfunktionellen Molekülen über metallierte Dimethylhydrazone Wikidata
Synthesis of 1,n-Dicarbonyl Derivates Using Carbanions from 1,3-Dithianes Wikidata
Synthesis of a limonoid, azadiradione Wikidata
Synthesis of novel macrocyclic lactones in the prostaglandin and polyether antibiotic series Wikidata
The Synthesis of Olefins from O,O'-Dialkyl β-Lithioalkylphosphonothioate Esters Wikidata
Total synthesis and absolute configuration of 7,20-diisocyanoadociane Wikidata
Total synthesis of (.+-.)-antheridium-inducing factor (AAn) of the Fern Anemia phyllitidis. Clarification of stereochemistry Wikidata
THE TOTAL SYNTHESIS OF A 5-PHENYL PENICILLIN: METHYL 5-PHENYL-(2-CARBOMETHOXYETHYL)-PENICILLINATE Wikidata
Total synthesis of prostaglandins E2 and F2α () via a tricarbocyclic intermediate Wikidata
Total synthesis of (S)-12-hydroxy-5,8,14-cis,-10-trans-eicosatetraenoic acid (Samuelsson's HETE) Wikidata
Total Synthesis ofd,l-Caryophyllene andd,l-Isocaryophyllene Wikidata
Useful new organometallic reagents for the synthesis of allylic alcohols by nucleophilic vinylation Wikidata
Useful procedures for the oxidation of alcohols involving pyridinium dichromate in aprotic media Wikidata
X-Ray crystal structure of a chiral oxazaborolidine catalyst for enantioselective carbonyl reduction Wikidata
X-ray crystallographic studies provide additional evidence that an enzyme-like binding pocket is crucial to the enantioselective dihydroxylation of olefins by OsO4—bis-cinchona alkaloid complexes Wikidata
コーリー有機合成のコンセプト NII (Japan)

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