Total synthesis of (-)-(6R,11R,14S)-colletallol via proline catalyzed alpha-aminoxylation and Yamaguchi macrolactonization
Title | Total synthesis of (-)-(6R,11R,14S)-colletallol via proline catalyzed alpha-aminoxylation and Yamaguchi macrolactonization |
Publication Type | Journal Article |
Year of Publication | 2016 |
Authors | Kauloorkar, SVandana, Kumar, P |
Journal | RSC Advances |
Volume | 6 |
Issue | 68 |
Pagination | 63607-63612 |
Date Published | JUN |
ISSN | 2046-2069 |
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. |
DOI | 10.1039/c6ra08484b |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 3.289 |
Divison category:
Organic Chemistry