Highly diastereoselective Michael reaction of ( S )-mandelic acid enolate. Chiral benzoyl carbanion equivalent through an oxidative decarboxylation of α-hydroxyacids-Reference-Cited by-同舟云学术

Highly diastereoselective Michael reaction of ( S )-mandelic acid enolate. Chiral benzoyl carbanion equivalent through an oxidative decarboxylation of α-hydroxyacids

Published:2002-11 Issue:47 Volume:43 Page:8463-8466
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Blay Gonzalo,Fernández Isabel,Monje Belén,Pedro José R,Ruiz Rafael

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference20 articles.

1. Jung, H. E. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 4, Chapter 1.1, p. 1

2. Conjugate Addition Reactions in Organic Synthesis;Perlmuter,1992

3. The asymmetric Michael addition reactions using chiral imines

4. Asymmetric conjugate addition

5. Phosphoramidites: Marvellous Ligands in Catalytic Asymmetric Conjugate Addition

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