Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance upgrade on Thursday 4th of May 2017 from 8.00am to 9.00am (BST).

During this time our websites will be offline temporarily. If you have any questions please use the feedback button on this page. We apologise for any inconvenience this might cause and thank you for your patience.



Transition-metal-free oxidative reaction of hydrazines and potassium metabisulfite for preparation of sulfonohydrazides

Author affiliations

Abstract

A transition-metal-free oxidative coupling reaction for the synthesis of sulfonohydrazides from two types of hydrazines and potassium metabisulfite under air has been developed. This highly selective reaction used one arylhydrazine as an aryl coupling partner and potassium metabisulfite as a sulfur dioxide precursor, which provides a new and green strategy to sulfonohydrazides.

Graphical abstract: Transition-metal-free oxidative reaction of hydrazines and potassium metabisulfite for preparation of sulfonohydrazides

Back to tab navigation
Please wait while Download options loads

Supplementary files

Publication details

The article was received on 02 Mar 2017, accepted on 22 Mar 2017 and first published on 23 Mar 2017


Article type: Research Article
DOI: 10.1039/C7QO00168A
Citation: Org. Chem. Front., 2017, Advance Article
  •   Request permissions

    Transition-metal-free oxidative reaction of hydrazines and potassium metabisulfite for preparation of sulfonohydrazides

    Y. Wang, B. Du, W. Sha, H. Mei, J. Han and Y. Pan, Org. Chem. Front., 2017, Advance Article , DOI: 10.1039/C7QO00168A

Search articles by author