Abstract
AbstractDivergent syntheses of two 14‐membered resorcylic acid lactones (RALs), cochliomycin B (6) and zeaenol (22), have been accomplished. The key feature in our strategy was the facile construction of three contiguous stereogenic centers in the title molecules by using natural L‐arabinose as the chiral template. The key reactions included Takai olefination, Suzuki cross coupling, transesterification, and a late‐stage ring‐closing metathesis (RCM).
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
