Total synthesis of integrastatin B enabled by a benzofuran oxidative dearomatization cascade
Title | Total synthesis of integrastatin B enabled by a benzofuran oxidative dearomatization cascade |
Publication Type | Journal Article |
Year of Publication | 2016 |
Authors | More, AA, Ramana, CV |
Journal | Organic Letters |
Volume | 18 |
Issue | 6 |
Pagination | 1458-1461 |
Date Published | MAR |
ISSN | 1523-7060 |
Abstract | The first total synthesis of integrastatin B, a potent HIV-1 integrase inhibitor, has been accomplished in seven steps with a 17.9% overall yield employing easily accessible starting compounds. The Oxone-mediated oxidative benzofuran dearomatization cascade has been employed as the key skeletal construct to forge the central tetracyclic nucleus. |
DOI | 10.1021/acs.orglett.6b00404 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 6.732 |
Divison category:
Organic Chemistry