1071956-71-2Relevant academic research and scientific papers
Total synthesis of amphidinolide J
Barbazanges, Marion,Meyer, Christophe,Cossy, Janine
, p. 4489 - 4492 (2008)
(Chemical Equation Presented) The marine natural product amphidinolide J has been synthesized according to a convergent strategy. The key steps of this synthesis include a B-alkyl Suzuki-Miyaura coupling and the addition of an alkynyllithium reagent to a Weinreb amide to build the C4-C5 and C12-C13 bonds, respectively, and a Yamaguchi macrolactonization.
