Abstract
As exemplified by the isomerisation of N-allylacetamide in the presence of hydridocarbonyl complexes (μ-H)Os3(μ-OCNR1R2)(CO)10 (R1 = H, Alk; R2 = Alk), it has been demonstrated for the first time that they are effective catalysts for the [1,2]-double bond shift under mild conditions in allylic compounds functionalised with an amido group.
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