Oxidative carbonylation of 1,5-cyclooctadiene in methylene chloride-methanol mixture, catalyzed by Pd(II)-salts, gave rise to a bicyclic, bifunctional product under mild experimental conditions. The mechanism, involving multiple carbon monoxide and double bond insertions into the Pd(II)-carbon σ-bond, has been proposed, as being consistent with the outcome of this novel ring closure reaction.
在甲基氯仿-甲醇混合物中,由Pd(II)盐催化的1,5-环辛二烯的氧化羰基化反应在温和的实验条件下形成了一种双环,双功能产物。已经提出了多个一氧化碳和双键插入到Pd(II)-碳σ键的机理,这与这种新型环闭合反应的结果一致。