Enantioselective organocatalytic epoxidation driven by electrochemically generated percarbonate and persulfate

P C B Page, F Marken, C Williamson, Y Chan, B R Buckley, D Bethell

Research output: Contribution to journalArticle

38 Citations (Scopus)

Abstract

An organocatalytic asymmetric epoxidation reaction using iminium salt catalysts is described, in which the stoichiometric persulfate oxidant is generated electrochemically. This system offers comparable ees to the use of commercially available persulfate. Electrochemically generated percarbonate ion is also a successful and novel oxidant system for use with iminium salts.
Original languageEnglish
Pages (from-to)1149-1154
Number of pages6
JournalAdvanced Synthesis & Catalysis
Volume350
Issue number7-8
DOIs
Publication statusPublished - 2008

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Epoxidation
Oxidants
Salts
Ions
Catalysts
sodium percarbonate

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Enantioselective organocatalytic epoxidation driven by electrochemically generated percarbonate and persulfate. / Page, P C B; Marken, F; Williamson, C; Chan, Y; Buckley, B R; Bethell, D.

In: Advanced Synthesis & Catalysis, Vol. 350, No. 7-8, 2008, p. 1149-1154.

Research output: Contribution to journalArticle

Page, P C B ; Marken, F ; Williamson, C ; Chan, Y ; Buckley, B R ; Bethell, D. / Enantioselective organocatalytic epoxidation driven by electrochemically generated percarbonate and persulfate. In: Advanced Synthesis & Catalysis. 2008 ; Vol. 350, No. 7-8. pp. 1149-1154.
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