869385-99-9Relevant academic research and scientific papers
Novel "protecting group-dependent" alkylation-RCM strategy to medium-sized oxacycles: First total synthesis of (-)-isoprelaurefucin
Lee, Hyunjoo,Kim, Hyoungsu,Yoon, Taehyun,Kim, Byungsook,Kim, Sanghee,Kim, Hee-Doo,Kim, Deukjoon
, p. 8723 - 8729 (2007/10/03)
A novel "protecting group-dependent" alkylation strategy was developed for complementary diastereoselective syntheses of α, α′-syn- and α,α′-anti-bis-alkenes 2 and 3, which represent ring-closing metathesis (RCM) substrates for medium-sized oxacycles. This principle has been applied to a stereoselective and concise total synthesis of (-)-isoprelaurefucin (4) in 14 steps in 12% overall yield from known epoxide 8.
