629645-73-4Relevant academic research and scientific papers
Total synthesis of brevetoxin B
Kadota, Isao,Takamura, Hiroyoshi,Nishii, Hiroki,Yamamoto, Yoshinori
, p. 9246 - 9250 (2007/10/03)
The convergent total synthesis of brevetoxin B (1) has been achieved. The intramolecular allylation of the O,S-acetal 20, prepared from the α-chlorosulfide 17 and the alcohol 5, was carried out using AgOTf as a Lewis acid to give the diene 21, predominant
Convergent synthesis of the F-K ring segment of brevetoxin B
Kadota, Isao,Nishina, Naoko,Nishii, Hiroki,Kikuchi, Shigetoshi,Yamamoto, Yoshinori
, p. 7929 - 7932 (2007/10/03)
A convergent synthesis of the F-K ring segment of brevetoxin B has been achieved via the intramolecular allylation of an α-chloroacetoxy ether and subsequent ring-closing metathesis.
