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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...

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Detalles Bibliográficos
Autores principales: Huang, Xiaoqiang, Li, Xinyao, Jiao, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
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.
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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
title_full Copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative N-incorporation
title_fullStr Copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative N-incorporation
title_full_unstemmed Copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative N-incorporation
title_short Copper-catalyzed direct transformation of simple alkynes to alkenyl nitriles via aerobic oxidative N-incorporation
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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AT jiaoning coppercatalyzeddirecttransformationofsimplealkynestoalkenylnitrilesviaaerobicoxidativenincorporation