Abstract
The first synthesis of 6,5,5,5-tetracyclic moiety related with promising anti-HIV activity in rubriflordilactone B has been efficiently achieved. Our strategy started from cheap materials, and features the utilization of radical 1,5-H abstraction/cyclization and vinylogous Mukaiyama aldol reaction, which successfully established the array of five continuous stereogenic carbon centers in the target.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
