Issue 59, 2018

Arylhydrazines: novel and versatile electrophilic partners in cross-coupling reactions

Abstract

Arylhydrazines are extremely valuable compounds in organic chemistry that are widely used for the synthesis of a variety of biologically active molecules such as indoles, indazoles, pyrazoles, aryltriazoles, β-lactams and quinazolines. These compounds have also been widely utilized as arylation agents in oxidative cross-coupling reactions. In this review, we will highlight the most important explorations and developments in the carbon–carbon and carbon–heteroatom (nitrogen, phosphorus, sulfur, and selenium) cross-coupling of arylhydrazines. The literature has been surveyed from 2001 to June 2018.

Graphical abstract: Arylhydrazines: novel and versatile electrophilic partners in cross-coupling reactions

Article information

Article type
Review Article
Submitted
30 Шіл. 2018
Accepted
06 Қыр. 2018
First published
01 Қаз. 2018
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2018,8, 33828-33844

Arylhydrazines: novel and versatile electrophilic partners in cross-coupling reactions

A. Hosseinian, R. Mohammadi, S. Ahmadi, A. Monfared and Z. Rahmani, RSC Adv., 2018, 8, 33828 DOI: 10.1039/C8RA06423G

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements