Asymmetric total synthesis of (2S,3S)-3-hydroxypipecolic acid

TitleAsymmetric total synthesis of (2S,3S)-3-hydroxypipecolic acid
Publication TypeJournal Article
Year of Publication2011
AuthorsChavan, SP, Dumare, NB, Harale, KR, Kalkote, UR
JournalTetrahedron Letters
Volume52
Issue3
Pagination404-406
Date PublishedJAN
ISSN0040-4039
Abstract

A synthetic route to (2S,3S)-3-hydroxypipecolic acid was achieved from readily available nonchiral pool starting material cis-2-butene-1,4-diol and involved Claisen orthoester rearrangement, Sharpless asymmetric dihydroxylation and intramolecular lactamisation of azido lactone as the key steps. (C) 2010 Elsevier Ltd. All rights reserved.

DOI10.1016/j.tetlet.2010.11.062
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)2.683
Divison category: 
Organic Chemistry