Issue 67, 2017

Catalyst-controlled site-selective asymmetric epoxidation of nerylamine and geranylamine derivatives

Abstract

Novel catalysts for site- and enantioselective epoxidation of nerylamine and geranylamine derivatives have been developed. Although mCPBA oxidation took place selectively at the more electron-rich double bond to give the 6,7-epoxides, these catalysts provide the 2,3-epoxides in moderate to high enantioselectivity via the oxidation of the relatively electron-deficient double bond.

Graphical abstract: Catalyst-controlled site-selective asymmetric epoxidation of nerylamine and geranylamine derivatives

Supplementary files

Article information

Article type
Communication
Submitted
20 Jun 2017
Accepted
19 Jul 2017
First published
19 Jul 2017

Chem. Commun., 2017,53, 9320-9323

Catalyst-controlled site-selective asymmetric epoxidation of nerylamine and geranylamine derivatives

T. Nobuta and T. Kawabata, Chem. Commun., 2017, 53, 9320 DOI: 10.1039/C7CC04809B

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