Reversal of the stereoselectivity of [4 + 2]-cycloadditions by co-ordination of the heterodienophile to a transition metal fragment

Abstract
Co-ordination of thio- and selenoaldehydes to a pentacarbonylmetal fragment results in a reversal of the endo selectivity in Diels–Alder reactions with conjugated cyclic dienes giving predominantly exo adducts.

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