Asymmetric michael reaction via chiral α,β-unsaturated aldimines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. Asymmetric syntheses using tert-leucine. 1. An asymmetric synthesis of .beta.-substituted aldehydes via 1,4-addition of Grignard reagents to chiral .alpha.,.beta.-unsaturated aldimines
2. Asymmetric synthesis using α,β-unsaturated sulfoxides.
3. Asymmetric induction in the alkaloid-catalysed Michael reaction
4. The Stereochemistry of the Wolff Rearrangement
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1. A domino reaction of a β-ketoester, phenylethylamine and ethyl glyoxylate: leading to chiral tricarboxylate containing multiple stereocenters;Tetrahedron: Asymmetry;2008-11
2. New Concepts for Organocatalysis;Ernst Schering Foundation Symposium Proceedings;2008
3. Stereochemistry of the Base-Promoted Michael Addition Reaction;Topics in Stereochemistry;2007-02-26
4. tert-Leucinetert-Butyl Ester;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
5. Synthesis and use of enantiomerically pure tert-leucine;Tetrahedron: Asymmetry;1995-12
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