期刊:Synlett [Thieme Medical Publishers (Germany)] 日期:2016-04-20卷期号:27 (10): 1443-1449被引量:28
标识
DOI:10.1055/s-0035-1561619
摘要
Hyperforin has remained a popular and challenging synthetic target since its isolation over forty years ago. As a result, numerous synthetic strategies and ring-forming reactions have been developed to address its formidable molecular architecture. Herein we describe our contributions to this area resulting in a ten-step synthetic pathway enabled by a novel diketene annulation reaction and oxidative ring expansion strategy.