Sulfinyl-Mediated Stereoselective Overman Rearrangements and Diels-Alder Cycloadditions

J Org Chem. 2016 May 20;81(10):4081-97. doi: 10.1021/acs.joc.6b00365. Epub 2016 Apr 29.

Abstract

Sulfinyl trichloroacetamides are readily obtained in excellent yields through a highly stereoselective Overman rearrangement. Related bis-allylic substrates lead to amido 2-sulfinyl butadiene derivatives in excellent yields, with total chemo- and diastereoselectivity. These amido dienyl sulfoxides undergo highly selective Diels-Alder cycloadditions with N-phenylmaleimide with remarkable stereocontrol by the sulfoxide moiety.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.