Total synthesis of mangiferaelactone

TitleTotal synthesis of mangiferaelactone
Publication TypeJournal Article
Year of Publication2014
AuthorsVadhadiya, PM, Ramana, CV
JournalTetrahedron Letters
Volume55
Issue45
Pagination6263-6265
Date PublishedNOV
ISSN0040-4039
KeywordsBernet-Vasella fragmentation, Nonenolide, Ring closing metathesis, Total synthesis, Yamaguchi protocol
Abstract

Herein we document the first total synthesis of mangiferaelactone and thus establish its absolute configuration. The central nonenolide ring was constructed using ring closing metathesis and Yamaguchi esterification. The key alcohol fragment was synthesized by the Bernet-Vasella fragmentation of C-ribofuranoside. (C) 2014 Elsevier Ltd. All rights reserved.

DOI10.1016/j.tetlet.2014.09.084
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)2.68
Divison category: 
Organic Chemistry