Stereoselective Barbier-Type Allylations and Propargylations Mediated by CpTiCl3

J Org Chem. 2019 Jan 18;84(2):806-816. doi: 10.1021/acs.joc.8b02643. Epub 2019 Jan 4.

Abstract

CpTiCl2, prepared in situ by manganese reduction of CpTiCl3, is an excellent new system for the Barbier-type allylation and propargylation of carbonyl compounds. It can be used in catalytic amounts when combined with Et3N·HBr/TMSBr, which acts as a regenerating system. The high regio- and stereoselectivity shown by this system makes it useful for prenylation and crotylation processes in the synthesis of natural products.

Publication types

  • Research Support, Non-U.S. Gov't