Total synthesis of (-)-(6R,11R,14S)-colletallol via proline catalyzed alpha-aminoxylation and Yamaguchi macrolactonization

TitleTotal synthesis of (-)-(6R,11R,14S)-colletallol via proline catalyzed alpha-aminoxylation and Yamaguchi macrolactonization
Publication TypeJournal Article
Year of Publication2016
AuthorsKauloorkar, SVandana, Kumar, P
JournalRSC Advances
Volume6
Issue68
Pagination63607-63612
Date PublishedJUN
ISSN2046-2069
Abstract

A simple and efficient synthesis of the 14-membered macrolide (-)-(6R,11R,14S)-colletallol was achieved in a highly diastereoselective manner with high overall yield. The stereogenic centre was generated using a proline catalyzed alpha-aminoxylation reaction and the ring was constructed using Yamaguchi protocol.

DOI10.1039/c6ra08484b
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)3.289
Divison category: 
Organic Chemistry