Journal of Molecular Catalysis A-Chemical, Vol.178, No.1-2, 27-33, 2002
Cyclopropanation of styrene with diazoacetates catalyzed by copper and rhodium complexes of new chiral 2,2': 6',2"-terpyridines derived from natural occurring compounds
Three new chiral 2,2': 6',2"-terpyridines (terpy) were prepared from (-)-beta-pinene, (+)-camphor and (+)-2-carene and the corresponding copper and rhodium complexes were assessed as chiral catalysts for the enantioselective cyclopropanation of styrene with diazoacetates. Enantioselectivities up to 64% were obtained. (C) 2002 Elsevier Science B.V. All rights reserved.
Keywords:chiral terpyridines;copper complex;rhodium complex;cyclopropanation reaction;enantioselectivity