摘要
以己二酸为起始原料,成功地合成了有手性季碳中心的内酯化合物(—)-Mialyngolide(1),其中关键的步骤采用手性相转移催化剂进行立体选择烷基化反应,此合成路线短,总收率为10.5%。
The title compound had
been synthesized from adipic acid(starting material) ineight stepe,in
10.5% over all yield.A chiral phase transfer catalyst was used to
promote the stereose-lectivity alkylation reactions in the key steps
of forming chiral centers.
出处
《药学学报》
CAS
CSCD
北大核心
1994年第9期680-683,共4页
Acta Pharmaceutica Sinica
关键词
Malyngolide
合成
催化
烷基化
Malyngolide total synthesis
Phase transfer catalysis
Stereoselectivity alkylation