The first synthesis of chiral phosphinocarboxylic acid ligands, trans-2-(diphenylphosphino)cycloalkanecarboxylic acids. The phosphine-palladium complexes catalyzed asymmetric allylic alkylation-Reference-Cited by-同舟云学术

The first synthesis of chiral phosphinocarboxylic acid ligands, trans-2-(diphenylphosphino)cycloalkanecarboxylic acids. The phosphine-palladium complexes catalyzed asymmetric allylic alkylation

Published:1990-01 Issue:27 Volume:31 Page:3905-3908
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Okada Yoshiharu,Minami Toru,Sasaki Yoritaka,Umezu Yasuo,Yamaguchi Masahiko

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. A preliminary account of these results has been reported at 16th Symposium on Organic Sulfur and Phosphorus Chemistry of the Chemical Society of Japan, Morioka, January, 1989; abstract p. 131.

2. Asymmetric Catalytic Hydrogenation with an Optically Active Phosphinerhodium Complex in Homogeneous Solution

3. Asymmetric catalytic reduction with transition metal complexes. I. Catalytic system of rhodium(I) with (-)-2,3-0-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane, a new chiral diphosphine

4. Organopalladium intermediates in organic synthesis

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