Determination of the protons eliminated in the regioselective deprotonation of some optically active 3-keto steroids by a chiral lithium amide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Enantioselective deprotonation by chiral lithium amide bases: asymmetric synthesis of trimethylsilyl enol ethers from 4-alkylcyclohexanones
2. Enantioselective Deprotonation of the Meso-Forms of 2,6- and 3,5-Dimethylcyclohexanones
3. Crystallographic and lithium-6 and nitrogen-15 NMR studies of a chiral bidentate lithium amide. An effect of aggregation states on an enantioselective deprotonation reaction
4. Regioselective enolization of optically active 3-keto steroids using chiral lithium amides
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1. Alkylation and Acylation of Aldehydes, Ketones, and Their Derivatives;Comprehensive Organic Transformations;2018-02-28
2. Asymmetric Transformations by Deprotonation Using Chiral Lithium Amides;Organic Reactions;2012-05-15
3. Enolate, Azaenolate, and Organolithium Alkylations;Principles of Asymmetric Synthesis;2012
4. Asymmetric Deprotonations Using Chiral Lithium Amide Bases;Topics in Stereochemistry;2010-02-10
5. Stereocontrolled Total Synthesis of theStemona Alkaloid (−)-Stenine;Chemistry - A European Journal;2001-10-01
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