1185202-61-2Relevant academic research and scientific papers
Total synthesis of brevisamide
Fadeyi, Olugbeminiyi O.,Lindsley, Craig W.
, p. 3950 - 3952 (2009)
(Figure Presented) The second total synthesis of Brevisamide, a marine cyclic ether alkaloid from Karenla brevls, is reported. This streamlined synthesis proceeds in 21 steps, 14 steps longest linear sequence, in 5.2% overall yield and features a key Sml2 reductive cyclization step to access the tetrasubstituted pyran core.
