[1,3]/[1,4]-Sulfur atom migration in β-hydroxyalkylphosphine sulfides

Beilstein J Org Chem. 2020 Jan 21:16:88-105. doi: 10.3762/bjoc.16.11. eCollection 2020.

Abstract

β-Hydroxyalkylphosphine sulfides undergo [1,3]- or [1,4]-sulfur atom phosphorus-to-carbon migration in the presence of Lewis or Brønsted acids. The direction of sulfur atom migration depends on the type of acid used for the reaction. In the presence of a Brønsted acid, mainly [1,3]-rearrangement is observed, whereas a Lewis acid catalyzes the [1,4]-sulfur migration. To gain insight into the mechanism of these transformations, the stereochemistry of these rearrangements have been tested, along with the conduction of some control experiments and DFT calculations.

Keywords: Brønsted and Lewis acids; DFT; mechanistic studies; rearrangement; stereochemistry; sulfur atom migration.

Grants and funding

Financial support from the National Science Centre (research grant no. 2012/07/E/ST5/00544) is kindly acknowledged.