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

Authors :
Wu Lingzi
Jiang Yuanfeng
Zhang Xiaomin
Leopoldo Marcello
Huang Yue
L. Voll Marsha
Sun Lingli
Sun ShiLi
Zheng Guangya
H. Kameshwar Vivek
Zheng Hao
A. Colabufo Nicola
Lai Xingfei
E. Franke Niels
Chen Ruohong
Shao Xianfeng
Zhang Wenji
Cao Fanrong
M. Patil Vaishali
Sun Guo-Xiang
Chen Zhengjie
D. Pandareesh Mirazkar
M. Okwuchukwu Precious
Mastromarino Margherita
Zhao Guixia
Bandyopadhyay Debasish
Li Xiaorong
Zhou Lei
Lacivita Enza
Qi Gang
Golian Mehrdad
P. Hansom Simon
Masand Neeraj
Jan Blok Geert
Ea Vicki
Wu Dan
Yang Fuhua
Xia Jupei
Byrappa Kullaiah
Wang Yi-Ning
Li Qiuhua
S. Green Martin
Y.N. Schouten-van Meeteren Antoinette
Source :
Mini-Reviews in Organic Chemistry. 18:339-360
Publication Year :
2021
Publisher :
Bentham Science Publishers Ltd., 2021.

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.

Details

ISSN :
1570193X
Volume :
18
Database :
OpenAIRE
Journal :
Mini-Reviews in Organic Chemistry
Accession number :
edsair.doi...........e0a0542eb8b4f5ad4580ac1217ba5376