Highly enantioselective rearrangement of quaternary carbon-containing meso-epoxides to allylic alcohols
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference8 articles.
1. Asymmetric synthesis using homochiral lithium amide bases
2. A concise asymmetric synthesis of (−)-untenone A
3. Concise racemic and highly enantioselective approaches to key intermediates for the syntheses of carbocyclic nucleosides and pseudo-ribofuranoses: formal syntheses of carbovir
4. Asymmetric creation of quaternary carbon centers
5. Base-Promoted Isomerizations of Epoxides
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1. Enantioselective Epoxide Opening;Organic Reactions;2022-06-13
2. Preparing Unnatural Amino Acids;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2022
3. Formation of Alkenes by Elimination;Comprehensive Organic Transformations;2018-02-28
4. Asymmetric Transformations by Deprotonation Using Chiral Lithium Amides;Organic Reactions;2012-05-15
5. ChemInform Abstract: Highly Enantioselective Rearrangement of Quaternary Carbon-Containing meso-Epoxides to Allylic Alcohols.;ChemInform;2010-08-05
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