cis-Stilbene and (1α,2β,3α)-(2-Ethenyl-3-methoxycyclopropyl)benzene as Mechanistic Probes in the MnIII(salen)-Catalyzed Epoxidation: Influence of the Oxygen Source and the Counterion on the Diastereoselectivity of the Competitive Concerted and Radical-Type Oxygen Transfer

Abstract

cis-Stilbene (1) has been epoxidized by a set of diverse oxygen donors [OxD], catalyzed by the Mn^III(salen)X complexes 3 (X = Cl, PF₆), to afford a mixture of cis- and trans-epoxides 2. The cis/trans ratios range from 29:71 (extensive isomerization) to 92:8, which depends both on the oxygen source [OxD] and on the counterion X of the catalyst. When (1α,2β,3α)-(2-ethenyl-3-methoxycyclopropyl)-benzene (4) is used as substrate, a mechanistic probe which differentiates between radical and cationic intermediates, no cationic ring-opening products are found in this epoxidation reaction; thus, isomerized epoxide product arises from intermediary radicals. The dependence of the diastereoselectivity on the oxygen source is rationalized in terms of a bifurcation step in the catalytic cycle, in which concerted Lewis-acid-activated oxygen transfer competes with stepwise epoxidation by the established Mn^V(oxo) species. The experimental counterion effect is attributed to the computationally assessed ligand-dependent reaction profiles and stereoselectivities of the singlet, triplet, and quintet spin states available to the manganese species.