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

Autor: 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
Rok vydání: 2021
Předmět:
Zdroj: Mini-Reviews in Organic Chemistry. 18:339-360
ISSN: 1570-193X
Popis: 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.
Databáze: OpenAIRE