Collection of Czechoslovak Chemical Communications p. 2374 - 2382 (1992)
Update date:2022-08-03
Topics:
Anderson, Curtis B.
Markovic, Rade
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 ?-bond, has been proposed, as being consistent with the outcome of this novel ring closure reaction.
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