Asymmetric organocatalysis of epoxidation by iminium salts under non-aqueous conditions

Bulman Page, P. C. B., Buckley, B. R., Barros, D., Blacker, A. J., Marples, B. A. and Elsegood, M. R. J. (2007) Asymmetric organocatalysis of epoxidation by iminium salts under non-aqueous conditions. Tetrahedron, 63 (25). pp. 5386-5393. ISSN 0040-4020

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Abstract

Three iminium salts have been tested as catalysts for the asymmetric epoxidation of simple alkenes under non-aqueous conditions in various solvents, at varying temperatures, employing tetraphenylphosphonium monoperoxybisulfate (TPPP) as the stoichiometric oxidant. Enantiomeric excesses of up to 89% have been observed. (c) 2007 Elsevier Ltd. All rights reserved.

Item Type:	Article
Uncontrolled Keywords:	catalysts,enantioselective olefin epoxidation,alkene,unsaturated oxaziridines,oxone(r),mechanism,chiral oxaziridinium salt,oxidation,oxygen-transfer,epoxidation,intramolecular epoxidation
Faculty \ School:	Faculty of Science > School of Chemistry
UEA Research Groups:	Faculty of Science > Research Groups > Synthetic Chemistry (former - to 2017) Faculty of Science > Research Groups > Chemistry of Materials and Catalysis
Depositing User:	Rachel Smith
Date Deposited:	20 Jun 2011 13:51
Last Modified:	23 Oct 2022 07:30
URI:	https://ueaeprints.uea.ac.uk/id/eprint/32884
DOI:	10.1016/j.tet.2007.04.066

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