Asymmetric Synthesis XIII: The Stereocontrolled Synthesis of (R)—α—Amino Acids via a Double Chiral Induction-Reference-Cited by-同舟云学术

Asymmetric Synthesis XIII: The Stereocontrolled Synthesis of (R)—α—Amino Acids via a Double Chiral Induction

Published:1991-04 Issue:8-9 Volume:21 Page:1087-1090
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Zhong Jiang Yao,Guilan Liu,Changyou Zhou,Hauri Piao,Lanjun Wu,Aiqiao Mi

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397919108019799

Reference5 articles.

1. Asymmetric Synthesis. VII. Double Stereodifferentiation in Allylation of Ketimines Bearing Two Chiral Auxiliaries. Application to Enantioselective Synthesis of α-Allylglycine

2. Zhong, Jiang Yao, Guilan, Liu, Rounhua, Den and Shengde, Wu. 1985. “Abstract of the Third International Kyoto Conference on New Aspects of Organic Chemistry”. Nov18–-221985, Kyoto, Japan. pp.C–-29

3. Alkylation of camphor imines of glycinates. Diastereoselectivity as a function of electronic factors in the alkylating agent

4. Alkylation stereochemistry of camphor derivatives of glycinates. Double chiral induction with secondary halides.

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