Short enantioselective total synthesis of (R)- and (S)-pipecolic acid

TitleShort enantioselective total synthesis of (R)- and (S)-pipecolic acid
Publication TypeJournal Article
Year of Publication2014
AuthorsChavan, SP, Khairnar, LB, Chavan, PN, Kalbhor, DB
JournalTetrahedron-Asymmetry
Volume25
Issue16-17
Pagination1246-1251
Date PublishedSEP
ISSN0957-4166
Abstract

A convenient and practical total synthesis of (R)- and (S)-pipecolic acid has been achieved by utilizing chiral cis-aziridine-2-carboxylate as the common synthetic precursor. The synthesis involves regioselective reductive cleavage of the aziridine ring and Wittig olefination as key reactions. (C) 2014 Elsevier Ltd. All rights reserved.

DOI10.1016/j.tetasy.2014.08.001
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)1.88
Divison category: 
Organic Chemistry