909016-28-0Relevant articles and documents
Enantioselective synthesis of aurisides A and B, cytotoxic macrolide glycosides of marine origin
Suenaga, Kiyotake,Hoshino, Hiroshi,Yoshii, Takanori,Mori, Kazunori,Sone, Hiroki,Bessho, Yuhki,Sakakura, Akira,Hayakawa, Ichiro,Yamada, Kiyoyuki,Kigoshi, Hideo
, p. 7687 - 7698 (2007/10/03)
The enantioselective synthesis of aurisides A and B, macrolide glycosides of marine origin, was achieved by a convergent approach. The C1-C9 segment 4 was prepared from (R)-pantolactone, and the C10-C17 segment 14 was synthesized from (R)-glycidyl trityl
Synthesis of the aglycon of aurisides A and B, cytotoxic macrolide glycosides of marine origin
Sone, Hiroki,Suenaga, Kiyotake,Bessho, Yuhki,Kondo, Takashi,Kigoshi, Hideo,Yamada, Kiyoyuki
, p. 85 - 86 (2007/10/03)
The synthesis of the aglycon of aurisides A and B was achieved from (R)-pantolactone in 29 steps using the Nozaki reaction and the Yamaguchi macrolactonization as key steps.