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