Asymmetric aldol reaction of an isocyanoacetate with aldehydes bychiral ferrocenylphosphine-gold(I) complexes: Design and preparation of new efficient ferrocenylphosphine ligands-Reference-Cited by-同舟云学术

Asymmetric aldol reaction of an isocyanoacetate with aldehydes bychiral ferrocenylphosphine-gold(I) complexes: Design and preparation of new efficient ferrocenylphosphine ligands

Published:1987-01 Issue:49 Volume:28 Page:6215-6218
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ito Yoshihiko,Sawamura Masaya,Hayashi Tamio

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. Catalytic asymmetric aldol reaction: reaction of aldehydes with isocyanoacetate catalyzed by a chiral ferrocenylphosphine-gold(I) complex

2. Asymmetric Synthesis Catalyzed by Chiral Ferrocenylphosphine–Transition Metal Complexes. I. Preparation of Chiral Ferrocenylphosphines

3. Asymmetric synthesis catalyzed by transition-metal complexes with functionalized chiral ferrocenylphosphine ligands

4. 15. Preparation ofL-threonine. Interconversion of the four stereoisomeric α-amino-β-hydroxybutyric acids

5. A stereoselective synthesis of threo-threonine reaction of isocyanoacetate with acetaldehyde.

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