1256363-75-3Relevant academic research and scientific papers
Enantioselective synthesis of (-)-sclerophytin A by a stereoconvergent epoxide hydrolysis
Wang, Bin,Ramirez, Armando P.,Slade, Justin J.,Morken, James P.
, p. 16380 - 16382 (2010)
The cytotoxic natural product (-)-sclerophytin A was constructed in 13 steps from geranial. Highlights from the synthesis are a stereoselective Oshima-Utimoto reaction, a Shibata-Baba indium-promoted radical cyclization, and a novel stereoconvergent epoxide hydrolysis.
