Organocatalysis of asymmetric epoxidation mediated by iminium salts: comments on the mechanism

Philip C. Bulman Page; David Barros; Benjamin R. Buckley; Brian A. Marples

doi:10.1016/j.tetasy.2005.08.053

Organocatalysis of asymmetric epoxidation mediated by iminium salts: comments on the mechanism

Philip C. Bulman Page, David Barros, Benjamin R. Buckley, Brian A. Marples

Research output: Contribution to journal › Article › peer-review

32 Citations (Scopus)

Abstract

Non-aqueous conditions developed for catalytic asymmetric epoxidation mediated by iminium salt organocatalysts have allowed NMR spectroscopy to be carried out on the reaction mixtures for the first time. (c) 2005 Elsevier Ltd. All rights reserved.

Original language	English
Pages (from-to)	3488-3491
Number of pages	4
Journal	Tetrahedron: Asymmetry
Volume	16
Issue number	21
DOIs	https://doi.org/10.1016/j.tetasy.2005.08.053
Publication status	Published - 2005

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10.1016/j.tetasy.2005.08.053

Cite this

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title = "Organocatalysis of asymmetric epoxidation mediated by iminium salts: comments on the mechanism",

abstract = "Non-aqueous conditions developed for catalytic asymmetric epoxidation mediated by iminium salt organocatalysts have allowed NMR spectroscopy to be carried out on the reaction mixtures for the first time. (c) 2005 Elsevier Ltd. All rights reserved.",

author = "{Bulman Page}, {Philip C.} and David Barros and Buckley, {Benjamin R.} and Marples, {Brian A.}",

year = "2005",

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language = "English",

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journal = "Tetrahedron: Asymmetry",

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AU - Bulman Page, Philip C.

AU - Barros, David

AU - Buckley, Benjamin R.

AU - Marples, Brian A.

PY - 2005

Y1 - 2005

N2 - Non-aqueous conditions developed for catalytic asymmetric epoxidation mediated by iminium salt organocatalysts have allowed NMR spectroscopy to be carried out on the reaction mixtures for the first time. (c) 2005 Elsevier Ltd. All rights reserved.

AB - Non-aqueous conditions developed for catalytic asymmetric epoxidation mediated by iminium salt organocatalysts have allowed NMR spectroscopy to be carried out on the reaction mixtures for the first time. (c) 2005 Elsevier Ltd. All rights reserved.

U2 - 10.1016/j.tetasy.2005.08.053

DO - 10.1016/j.tetasy.2005.08.053

M3 - Article

SN - 0957-4166

VL - 16

SP - 3488

EP - 3491

JO - Tetrahedron: Asymmetry

JF - Tetrahedron: Asymmetry

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ER -