Issue 36, 2021, Issue in Progress

A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate

Abstract

The efficient formation of tert-butyl N-chloro-N-sodio-carbamate by the reaction of simple tert-butyl carbamate with sodium hypochlorite pentahydrate (NaOCl·5H2O) would be a practical and green method for the aziridination of α,β-unsaturated carbonyl compounds. The process described herein is transition-metal free, all of the materials are commercially available, the byproducts (NaCl and H2O) are environmentally benign and the reaction is stereoselective. The resulting aziridines are potential precursors of amino acids.

Graphical abstract: A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate

Supplementary files

Article information

Article type
Paper
Submitted
03 Jun 2021
Accepted
17 Jun 2021
First published
22 Jun 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 22120-22124

A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate

T. Umeda and S. Minakata, RSC Adv., 2021, 11, 22120 DOI: 10.1039/D1RA04297A

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