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1,2-Difunctionalizations of alkynes entailing concomitant C–C and C–N bond-forming carboamination reactions
Vicinal carboamination of alkynes is a highly reliable and efficient practical strategy for the quick preparation of valuable and diverse amine derivatives starting from simple synthons. The last decade has witnessed numerous practical methods employing transition-metal-based/metal-free carboaminati...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981577/ https://www.ncbi.nlm.nih.gov/pubmed/35424576 http://dx.doi.org/10.1039/d1ra06633a |
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author | Nanda, Santosh Kumar Mallik, Rosy |
author_facet | Nanda, Santosh Kumar Mallik, Rosy |
author_sort | Nanda, Santosh Kumar |
collection | PubMed |
description | Vicinal carboamination of alkynes is a highly reliable and efficient practical strategy for the quick preparation of valuable and diverse amine derivatives starting from simple synthons. The last decade has witnessed numerous practical methods employing transition-metal-based/metal-free carboamination approaches using alkynes for the synthesis of these N-bearing entities. Driven by the renaissance of transition metal catalysis, intermolecular and intramolecular carboamination of alkynes comprising concomitant C–N and C–C bond formation has been studied extensively. In contrast to metal catalysis, though analogous metal-free approaches have been relatively less explored in the literature, they serve as alternatives to these expensive approaches. Despite this significant progress, reviews documenting such examples are sporadic; as a result, most reports of this type remained scattered throughout the literature, thereby hampering further developments in this escalating field. In this review, different conceptual approaches will be discussed and examples from the literature will be presented. Further, the reader will get insight into the mechanisms of different transformations. |
format | Online Article Text |
id | pubmed-8981577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-89815772022-04-13 1,2-Difunctionalizations of alkynes entailing concomitant C–C and C–N bond-forming carboamination reactions Nanda, Santosh Kumar Mallik, Rosy RSC Adv Chemistry Vicinal carboamination of alkynes is a highly reliable and efficient practical strategy for the quick preparation of valuable and diverse amine derivatives starting from simple synthons. The last decade has witnessed numerous practical methods employing transition-metal-based/metal-free carboamination approaches using alkynes for the synthesis of these N-bearing entities. Driven by the renaissance of transition metal catalysis, intermolecular and intramolecular carboamination of alkynes comprising concomitant C–N and C–C bond formation has been studied extensively. In contrast to metal catalysis, though analogous metal-free approaches have been relatively less explored in the literature, they serve as alternatives to these expensive approaches. Despite this significant progress, reviews documenting such examples are sporadic; as a result, most reports of this type remained scattered throughout the literature, thereby hampering further developments in this escalating field. In this review, different conceptual approaches will be discussed and examples from the literature will be presented. Further, the reader will get insight into the mechanisms of different transformations. The Royal Society of Chemistry 2022-03-04 /pmc/articles/PMC8981577/ /pubmed/35424576 http://dx.doi.org/10.1039/d1ra06633a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Nanda, Santosh Kumar Mallik, Rosy 1,2-Difunctionalizations of alkynes entailing concomitant C–C and C–N bond-forming carboamination reactions |
title | 1,2-Difunctionalizations of alkynes entailing concomitant C–C and C–N bond-forming carboamination reactions |
title_full | 1,2-Difunctionalizations of alkynes entailing concomitant C–C and C–N bond-forming carboamination reactions |
title_fullStr | 1,2-Difunctionalizations of alkynes entailing concomitant C–C and C–N bond-forming carboamination reactions |
title_full_unstemmed | 1,2-Difunctionalizations of alkynes entailing concomitant C–C and C–N bond-forming carboamination reactions |
title_short | 1,2-Difunctionalizations of alkynes entailing concomitant C–C and C–N bond-forming carboamination reactions |
title_sort | 1,2-difunctionalizations of alkynes entailing concomitant c–c and c–n bond-forming carboamination reactions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981577/ https://www.ncbi.nlm.nih.gov/pubmed/35424576 http://dx.doi.org/10.1039/d1ra06633a |
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