Abstract
A large set of copper complexes, prepared in situ from copper(I)-triflate and a variety enantiopure oxazoline ligands, was assessed as chiral catalysts in the enantioselective cyclopropanation of styrene by ethyl diazoacetate. Enantioselectivities up to 60% and up to 52%, respectively, for trans- and cis-2-phenylcyclopropanecarboxylate were observed.
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