Issue 44, 2017

Enabling the facile conversion of acyl hydrazides into N-acyl carbamates via metal-free ionic-based rupture of the N–N linkage

Abstract

Herein we report the one-pot transformation of readily synthesised/easily accessed acyl hydrazides into N-acyl carbamates via an alkylation-elimination reaction sequence. A range of N-acyl carbamates are prepared in consistent yields, including those featuring protecting groups and having alkyl & aryl N-acyl functionality. The reaction conditions also tolerate a wide variety of sensitive functional groups.

Graphical abstract: Enabling the facile conversion of acyl hydrazides into N-acyl carbamates via metal-free ionic-based rupture of the N–N linkage

Supplementary files

Article information

Article type
Paper
Submitted
12 Apr 2017
Accepted
17 May 2017
First published
23 May 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 27608-27611

Enabling the facile conversion of acyl hydrazides into N-acyl carbamates via metal-free ionic-based rupture of the N–N linkage

A. Shamsabadi, J. Ren and V. Chudasama, RSC Adv., 2017, 7, 27608 DOI: 10.1039/C7RA04178K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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