Enantioselective synthesis of (R)-(+)-alpha-lipoic acid via proline-catalyzed sequential alpha-aminoxylation and HWE olefination of aldehyde

TitleEnantioselective synthesis of (R)-(+)-alpha-lipoic acid via proline-catalyzed sequential alpha-aminoxylation and HWE olefination of aldehyde
Publication TypeJournal Article
Year of Publication2010
AuthorsPanchgalle, SP, Jogdand, GF, Chavan, SP, Kalkote, UR
JournalTetrahedron Letters
Volume51
Issue27
Pagination3587-3589
Date PublishedJUL
ISSN0040-4039
Abstract

An efficient enantioselective synthesis of (R)-(+)-alpha-lipoic acid is described, in high optical purity (>97% ee), using L-proline-catalyzed sequential alpha-aminoxylation and Horner-Wadsworth-Emmons olefination of aldehyde as the key step. (C) 2010 Elsevier Ltd. All rights reserved.

DOI10.1016/j.tetlet.2010.05.007
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)2.618
Divison category: 
Organic Chemistry