Asymmetric synthesis of both the enantiomers of trans-3-hydroxypipecolic acid

TitleAsymmetric synthesis of both the enantiomers of trans-3-hydroxypipecolic acid
Publication TypeJournal Article
Year of Publication2005
AuthorsKumar, P, Bodas, MS
JournalJournal of Organic Chemistry
Volume70
Issue1
Pagination360-363
Date PublishedJAN
Type of ArticleArticle
ISSN0022-3263
Abstract

Both the enantiomers of trans -3-hydroxypipecolic acid have been synthesized employing the Sharpless asymmetric di-hydroxylation and epoxidation as the key steps starting from a commercially available starting material 1,4-butanediol.

DOI10.1021/jo0485381
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

4.785

Divison category: 
Organic Chemistry