Halogen Atom Participation in Guiding the Stereochemical Outcomes of Acetal Substitution Reactions

Abstract

Acetal substitution reactions of α-halogenated five- and six-membered rings can be highly stereoselective. Erosion of stereoselectivity occurs as nucleophilicity increases, which is consistent with additions to a halogen-stabilized oxocarbenium ion, not a three-membered-ring halonium ion. Computational investigations confirmed that the open-form oxocarbenium ions are the reactive intermediates involved. Kinetic studies suggest that hyperconjugative effects and through-space electrostatic interactions can both contribute to the stabilization of halogen-substituted oxocarbenium ions.

Keywords: Diastereoselectivity; Glycosylation; Halonium Ion; Hyperconjugation; Oxocarbenium Ion.