1,3-Asymmetric induction in the aldol addition reactions of methyl ketone enolates and enolsilanes to β-substituted aldehydes. A model for chirality transfer-Reference-Cited by-同舟云学术

1,3-Asymmetric induction in the aldol addition reactions of methyl ketone enolates and enolsilanes to β-substituted aldehydes. A model for chirality transfer

Published:1994-11 Issue:46 Volume:35 Page:8537-8540
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Evans David A.,Duffy Joseph L.,Dart Michael J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference32 articles.

1. Studies in Stereochemistry. XXX. Models for Steric Control of Asymmetric Induction1

2. Structural, mechanistic, and theoretical aspects of chelation-controlled carbonyl addition reactions

3. Methodology to establish 1,2- and 1,3-difunctionality for the synthesis of carbohydrate derivates

4. Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones

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