Author:
Jones III Clifton W.,Leyden Donald E.,Stammer Charles H.
Abstract
An improved procedure for the synthesis of threo- and erythro-β-hydroxy-DL-aspartic acids is described. An nuclear magnetic resonance study of both diastereomers indicated that the threo isomer exists primarily as the conformer having anti carboxyl groups while the erythro compound prefers a conformation with gauche carboxyl functions. Possible reasons for this anomaly are presented.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
24 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献