286958-07-4Relevant articles and documents
Asymmetric synthesis of the A-ring part of ciguatoxin by the strategy based on diastereoselective hydroboration and ring closing metathesis
Fujiwara, Kenshu,Tanaka, Hideki,Murai, Akio
, p. 610 - 611 (2007/10/03)
Asymmetric synthesis of the A-ring part of a marine toxin ciguatoxin (CTX1 B) was achieved by the strategy based on ring closing metathesis (RCM), where introduction of the C5 asymmetric center was performed by diastereocontrolled hydroboration of a vinyl