立体中心
迈克尔反应
对映选择合成
分子内力
取代基
化学
立体化学
去甲基化
背景(考古学)
立体选择性
喹啉
组合化学
催化作用
有机化学
生物化学
基因表达
DNA甲基化
基因
古生物学
生物
作者
Etsuko Sekino,Takuya Kumamoto,Tomohiro Tanaka,Tomoko Ikeda,Tsutomu Ishikawa
摘要
(−)-Quinine-catalyzed intramolecular oxo-Michael addition (IMA) of 7-hydroxy-5-methoxy-8-tigloylcoumarins was developed for the enantioselective construction of 2,3-dimethyl-4-chromanone systems in the context of the asymmetric synthesis of anti-HIV-1 active Calophyllum coumarins. Combination of the IMA and MgI2-assisted demethylation of the 5-methoxy group along with isomerization of the formed chromanone systems as key steps successfully led to the concise synthesis of (+)-inophyllum B and (+)-calanolide A, possible candidates for AIDS drugs. Further examination of the asymmetric IMA with cinchona alkaloids lacking a methoxy group on the quinoline skeleton suggested the influence of the methoxy substituent on stereoselectivity at the stereogenic centers of the chromanone systems.
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