Syntheses of optically active pheromones with an epoxy ring, (+)-disparlure and both the enantiomers of (3z,6z)--9,10-epoxy-3,6-heneicosadiene
作者:Kenji Mori、Takashi Ebata
DOI:10.1016/s0040-4020(01)87314-2
日期:1986.1
(+)-Disparlure 1 and both the enantiomers of (3Z,6Z)-cis-9,10-epoxy-3, 6-heneicosadiene 2 were synthesized in optically pure forms employing the Sharpless asymmetric epoxidation as the key-step. The natural pheromone 2 isolated from Estigmene acrea was shown to possess (9S,10R)-stereochemistry.
以(Sharpless)不对称环氧化为关键步骤,以光学纯净的形式合成了(+)-Disparlure 1和(3Z,6Z)-cis-9,10-epoxy-3,6-heneicosadiene 2的对映体。分离自Estigmene acrea的天然信息素2具有(9S,10R)-立体化学。