1032746-46-5Relevant academic research and scientific papers
Gram scale synthesis of the C(1)-C(9) fragment of amphidinolide C
Morra, Nicholas A.,Pagenkopf, Brian L.
, p. 8632 - 8644 (2013/09/12)
An allylic cis-epoxide prepared by Sharpless asymmetric epoxidation was transformed in nine steps and 41% overall yield to the cyclization precursor 4 via a key one carbon homologation. Cobalt-catalyzed aerobic oxidative cyclization of 4 gave the trans-TH
An efficient strategy for the synthesis of endocyclic enol ethers and its application to the synthesis of spiroacetals
Fuwa, Haruhiko,Sasaki, Makoto
supporting information; experimental part, p. 2549 - 2552 (2009/05/26)
(Chemical Equation Presented) An efficient strategy for the synthesis of endocyclic enol ethers based on a Suzuki-Miyaura coupling/ring-closing metathesis sequence has been developed. The strategy has successfully been applied to the synthesis of spiroacetals, including cytotoxic marine metabolites attenols A and B.
