570402-53-8Relevant articles and documents
Short and flexible route to 3,4-diarylpyrrole marine alkaloids: Syntheses of permethyl storniamide A, ningalin B, and lamellarin G trimethyl ether
Iwao, Masatomo,Takeuchi, Toshiro,Fujikawa, Naotaka,Fukuda, Tsutomu,Ishibashi, Fumito
, p. 4443 - 4446 (2007/10/03)
A highly efficient route to 3,4-diarylpyrrole marine alkaloids has been developed using Hinsberg-type pyrrole synthesis and palladium-catalyzed Suzuki cross-coupling of the 3,4-dihydroxypyrrole bis-triflate derivatives as key reactions. Based on this approach, formal syntheses of permethyl storniamide A and ningalin B, and a total synthesis of lamellarin G trimethyl ether have been achieved.