Issue 22, 2016

Self-assembled ion-pair organocatalysis – asymmetric Baeyer–Villiger oxidation mediated by flavinium–cinchona alkaloid dimer

Abstract

An ion-pair catalyst generated by assembly of a chiral flavinium and a cinchona alkaloid dimer for use in asymmetric Baeyer–Villiger oxidation is presented. Ion-pair formation is essential for enhancing the catalytic activity and stereoselectivity. The catalyst is applicable to structurally diverse 3-substituted cyclobutanones, providing good to excellent enantioselectivities (up to 98 : 2 e.r.). This study provides the first example of self-assembly of a flavin derivative and a base to form a chiral reaction site that enables a highly stereoselective reaction to occur.

Graphical abstract: Self-assembled ion-pair organocatalysis – asymmetric Baeyer–Villiger oxidation mediated by flavinium–cinchona alkaloid dimer

Supplementary files

Article information

Article type
Communication
Submitted
23 Jan 2016
Accepted
17 Feb 2016
First published
19 Feb 2016

Chem. Commun., 2016,52, 4163-4166

Self-assembled ion-pair organocatalysis – asymmetric Baeyer–Villiger oxidation mediated by flavinium–cinchona alkaloid dimer

P. P. Poudel, K. Arimitsu and K. Yamamoto, Chem. Commun., 2016, 52, 4163 DOI: 10.1039/C6CC00663A

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