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Copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative N-incorporation
A novel direct transformation of aliphatic terminal alkynes to alkenyl nitriles through the incorporation of a nitrogen atom into the simple hydrocarbons has been reported. The usage of inexpensive copper catalyst, O(2) as the sole oxidant, broad substrate scope as well as feasibility for “late-stag...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054104/ https://www.ncbi.nlm.nih.gov/pubmed/30090253 http://dx.doi.org/10.1039/c5sc02126j |
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author | Huang, Xiaoqiang Li, Xinyao Jiao, Ning |
author_facet | Huang, Xiaoqiang Li, Xinyao Jiao, Ning |
author_sort | Huang, Xiaoqiang |
collection | PubMed |
description | A novel direct transformation of aliphatic terminal alkynes to alkenyl nitriles through the incorporation of a nitrogen atom into the simple hydrocarbons has been reported. The usage of inexpensive copper catalyst, O(2) as the sole oxidant, broad substrate scope as well as feasibility for “late-stage modification” make this protocol very promising. Mechanistic studies including DFT calculation demonstrate a novel 1,2-hydride shift process for this novel nitrogenation reaction. |
format | Online Article Text |
id | pubmed-6054104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-60541042018-08-08 Copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative N-incorporation Huang, Xiaoqiang Li, Xinyao Jiao, Ning Chem Sci Chemistry A novel direct transformation of aliphatic terminal alkynes to alkenyl nitriles through the incorporation of a nitrogen atom into the simple hydrocarbons has been reported. The usage of inexpensive copper catalyst, O(2) as the sole oxidant, broad substrate scope as well as feasibility for “late-stage modification” make this protocol very promising. Mechanistic studies including DFT calculation demonstrate a novel 1,2-hydride shift process for this novel nitrogenation reaction. Royal Society of Chemistry 2015-11-01 2015-07-20 /pmc/articles/PMC6054104/ /pubmed/30090253 http://dx.doi.org/10.1039/c5sc02126j Text en This journal is © The Royal Society of Chemistry 2015 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Huang, Xiaoqiang Li, Xinyao Jiao, Ning Copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative N-incorporation |
title | Copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative N-incorporation
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title_full | Copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative N-incorporation
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title_fullStr | Copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative N-incorporation
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title_full_unstemmed | Copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative N-incorporation
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title_short | Copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative N-incorporation
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title_sort | copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative n-incorporation |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054104/ https://www.ncbi.nlm.nih.gov/pubmed/30090253 http://dx.doi.org/10.1039/c5sc02126j |
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