4.2 Article

Cyclopropanation of styrene with diazoacetates catalyzed by copper and rhodium complexes of new chiral 2,2':6',2-terpyridines derived from natural occurring compounds

Journal

JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
Volume 178, Issue 1-2, Pages 27-33

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/S1381-1169(01)00287-4

Keywords

chiral terpyridines; copper complex; rhodium complex; cyclopropanation reaction; enantioselectivity

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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.

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