Chiral 2,6-bis(5',5'-diphenyloxazoline)pyridine as an efficient ligand for asymmetric catalysis

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Abstract

A modified tridentate pyridine bisoxazoline (pybox) ligand, possessing gemdiphenyl substitution at C-5 of the oxazoline rings, has been proved to be a very efficient ligand for enantioselective allylic oxidation, one-pot three-component synthesis of propargy - amines, and Friedel-Crafts alkylation of various aromatic compounds. We have shown that a 5',5'-diphenyl grouping in the oxazoline rings of chiral ligands is crucial for higher reaction rates as well as enhanced enantioselectivity. © 2012 IUPAC.

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Singh, P. K., & Singh, V. K. (2012). Chiral 2,6-bis(5’,5’-diphenyloxazoline)pyridine as an efficient ligand for asymmetric catalysis. Pure and Applied Chemistry, 84(7), 1651–1657. https://doi.org/10.1351/PAC-CON-11-10-16

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