Asymmetric synthesis of both the enantiomers of trans-3-hydroxypipecolic acid
Title | Asymmetric synthesis of both the enantiomers of trans-3-hydroxypipecolic acid |
Publication Type | Journal Article |
Year of Publication | 2005 |
Authors | Kumar, P, Bodas, MS |
Journal | Journal of Organic Chemistry |
Volume | 70 |
Issue | 1 |
Pagination | 360-363 |
Date Published | JAN |
Type of Article | Article |
ISSN | 0022-3263 |
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. |
DOI | 10.1021/jo0485381 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 4.785 |
Divison category:
Organic Chemistry