Highly enantioselective intramolecular Michael reactions by D-camphor-derived triazolium salts

Chem Commun (Camb). 2009 Oct 21:(39):5823-5. doi: 10.1039/b914805a. Epub 2009 Sep 8.

Abstract

Camphor-derived chiral triazolium salts have been found to be highly efficient for asymmetric intramolecular Michael reactions. With 1-5 mol% of the catalyst, the desired products were obtained in excellent yields, with up to 99% ee.