Indium-copper-mediated barbier-grignard-type alkylation reaction of imines in aqueous media

Org Lett. 2007 Dec 20;9(26):5413-6. doi: 10.1021/ol702263b. Epub 2007 Dec 1.

Abstract

An efficient system of In/CuI/InCl3 was developed for Barbier-Grignard-type alkylation reactions of simple imines, using a one-pot condensation of various aldehydes, amines (including aliphatic and chiral version), and alkyl iodides in water or aqueous media. The reactions proceeded efficiently at room temperature to give the desired products in moderate to good yields. Good diastereoselectivities were obtained when using L-valine methyl ester as substrate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Copper / chemistry*
  • Imines / chemistry*
  • Indicators and Reagents / chemistry*
  • Indium / chemistry*
  • Water / chemistry

Substances

  • Imines
  • Indicators and Reagents
  • Indium
  • Water
  • Copper