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Enantioselective Cyclopropanation of Styrene Catalysed by Copper(I) Complexes with Chiral Oxazolines
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- an...
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Published in: | Tetrahedron 2000-04, Vol.56 (18), p.2889-2893 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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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ISSN: | 0040-4020 1464-5416 |
DOI: | 10.1016/S0040-4020(00)00144-7 |