129848-97-1Relevant academic research and scientific papers
First stereoselective total synthesis of paecilomycin G
Bujaranipalli, Sheshurao,Das, Saibal
, p. 2800 - 2802 (2016)
The stereoselective total synthesis of resorcylic acid lactone, paecilomycin G (1) has been accomplished. The key steps involved are the Corey-Fuchs reaction, Sharpless asymmetric dihydroxylation, Jacobsen hydrolytic kinetic resolution, Stille coupling, Mitsunobu reaction, and Ring-closing metathesis (RCM) reaction.
