Add time:08/01/2019         Source:sciencedirect.com

Methylene interrupted dienes react with (naphthalene)(tricarbonyl)chromium under H2 to yield a mixture of positionally isomeric cis-monoene products. The isomer distribution, reactions with proposed organic intermediates, and kinetic studies suggest a mechanistic pathway that includes (1) loss of the arene from the metal fragment, (2) isomerization of the 1,4 diene to 1,3 conjugated dienes, and (3) subsequent reduction of the conjugated dienes to the isomeric cis-monoene products. The active metal fragment appears to be selective in the isomerization of 1,4 to 1,3 dienes and inert toward cis to trans geometrical isomerization of the monoene products. The results of kinetic studies using methyl cis,cis-9,12-octadecadienoate (methyl linoleate) as a substrate for the hydrogenation reactions are discussed.

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