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Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Johnson–Corey–Chaykovsky_reaction> ?p ?o }

• Johnson–Corey–Chaykovsky_reaction abstract "The Johnson–Corey–Chaykovsky reaction (sometimes referred to as the Corey–Chaykovsky reaction or CCR) is a chemical reaction used in organic chemistry for the synthesis of epoxides, aziridines, and cyclopropanes. It was discovered in 1961 by A. William Johnson and developed significantly by E. J. Corey and Michael Chaykovsky. The reaction involves addition of a sulfur ylide to a ketone, aldehyde, imine, or enone to produce the corresponding 3-membered ring. The reaction is diastereoselective favoring trans substitution in the product regardless of the initial stereochemistry. The synthesis of epoxides via this method serves as an important retrosynthetic alternative to the traditional epoxidation reactions of olefins.The reaction is most often employed for epoxidation via methylene transfer, and to this end has been used in several notable total syntheses (See Synthesis of epoxides below). Additionally detailed below are the history, mechanism, scope, and enantioselective variants of the reaction. Several reviews have been published.".
• Johnson–Corey–Chaykovsky_reaction thumbnail JCCRintro.png?width=300.
• Johnson–Corey–Chaykovsky_reaction wikiPageExternalLink File:J_C_C_startAnimGif.gif.
• Johnson–Corey–Chaykovsky_reaction wikiPageID "3249971".
• Johnson–Corey–Chaykovsky_reaction wikiPageLength "18816".
• Johnson–Corey–Chaykovsky_reaction wikiPageOutDegree "149".
• Johnson–Corey–Chaykovsky_reaction wikiPageRevisionID "707742428".
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink (E)-Stilbene.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Aldehyde.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Alicyclic_compound.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Aliphatic_compound.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Alkene.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Allyl.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Amide.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Amine.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Anomeric_effect.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Aryl.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Azetidine.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Aziridine.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Benzaldehyde.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Betaine.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Bicyclic_molecule.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink By-product.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Camphor.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Carbene.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Carbonyl.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Catalysis.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Category:Addition_reactions.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Category:Carbon-carbon_bond_forming_reactions.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Category:Epoxides.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Category:Name_reactions.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Chemical_reaction.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Chemotherapy.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Chirality_(chemistry).
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Conformational_isomerism.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Counterion.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Cycloaddition.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Cyclohexane_conformation.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Cyclopropane.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Danishefsky_Taxol_total_synthesis.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Darzens_reaction.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Density_functional_theory.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Diastereomer.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Dimethyl_sulfide.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Dimethyl_sulfoxide.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Double_bond.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Electrophile.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Elias_James_Corey.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Enantiomer.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Enantiomeric_excess.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Enone.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Epoxide.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Ester.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Ethylene_oxide.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Functional_group.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Heteroatom.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Homologation_reaction.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Imine.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink In_situ.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Ion.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Ketone.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Leaving_group.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Lithium.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Living_polymerization.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Lone_pair.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Methyl_group.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Methylene_(compound).
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Methylene_group.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Moiety_(chemistry).
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Nucleophile.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Nucleophilic_addition.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Nucleophilic_conjugate_addition.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Olefination.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Organic_chemistry.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Organoboron_chemistry.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Oxaziridine.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Oxetane.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Oxygen.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Paclitaxel.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Paclitaxel_total_synthesis.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Phosphazene.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Phosphorus.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Polar_effect.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Prelog_strain.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Rate-determining_step.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Reaction_mechanism.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Reaction_rate.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Retrosynthetic_analysis.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Rhodium.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Side_reaction.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Stereochemistry.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Steric_effects.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Stoichiometry.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Strychnine.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Strychnine_total_synthesis.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Sulfonium.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Total_synthesis.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Transition_metal_carbene_complex.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink Trimethylsulfonium.
• Johnson–Corey–Chaykovsky_reaction wikiPageWikiLink University_of_Bristol.

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