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Mini-Reviews in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-193X
ISSN (Online): 1875-6298

Review Article

Intermolecular Haloamination: Double Functionalization for Accesses to Vicinal Haloamines Involving Alkenes and Alkynes

Author(s): Yi-Ning Wang*, Gang Qi and Guo-Xiang Sun

Volume 18, Issue 3, 2021

Published on: 19 July, 2020

Page: [339 - 360] Pages: 22

DOI: 10.2174/1570193X17999200719134419

Price: $65

Abstract

Haloamination (or called aminohalogenation) upon the C-C unsaturated bonds is an important amino functionalization, which can introduce the halogen atoms accompanying with the amino groups into the substrate backbones in a tandem manner. Over the past two decades, it has drawn increasing attention due to its versatile applications. In this review, we will mainly focus on the synthetic strategies anchoring the intermolecular haloamination reactions achieved in the past few years. Limited by the length of the context, the intramolecular haloamination and the applications of the vicinal haloamines will not be involved.

Keywords: Addition, aminohalogenation, C-C unsaturated bonds, haloamination, intermolecular haloamination, vicinal haloamine.

Graphical Abstract


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