136459-95-5Relevant articles and documents
Efficient method for introducing vineomycin-fridamycin-type side chain. Total synthesis of fridamycin E
Matsumoto, Takashi,Jona, Hideki,Katsuki, Miyoko,Suzuki, Keisuke
, p. 5103 - 5106 (2007/10/02)
An effective approach for introducing vineomycin-fridamycin-type side chain was developed. Tin-lithium exchange of arylstannane 5 followed by the reaction with chiral aldehyde 6 gave the desired adduct 7. Total synthesis of (R)-(+)-fridamycin E was accomplished.