Asymmetric Synthesis Based on (2R,3S)-3,4-Dimethyl-2-phenylperhydro-1,4-oxazepine-5,7-dione. Synthesis of Highly Optically Active β-Substituted Alkanoic Acids-Reference-Cited by-同舟云学术

Asymmetric Synthesis Based on (2R,3S)-3,4-Dimethyl-2-phenylperhydro-1,4-oxazepine-5,7-dione. Synthesis of Highly Optically Active β-Substituted Alkanoic Acids

Published:1978-11 Issue:11 Volume:51 Page:3368-3372
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Mukaiyama Teruaki,Takeda Takeshi,Fujimoto Katsumi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/51/11/51_11_3368/_pdf

Reference15 articles.

1. N(Im)-Carbobenzoxyhistidine Derivatives as Intermediates for the Synthesis of Histidine Peptides1

2. Asymmetric Synthesis with Sugar Derivatives. I. The Conjugate Additions of Grignard Reagents to α, β-Unsaturated Esters of Sugar Derivatives

3. Oxazolines. XIX. Asymmetric synthesis of 3-substituted alkanoic acids via conjugated addition of organolithium reagents to chiral oxazolines

4. The Synthetic Utility of 2-Oxazolines

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