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Cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives
We describe copper-catalyzed cyanomethylation of imines and α,β-alkenes with a methylnitrile source and provide an efficient route to synthesize arylacrylonitriles and β,γ-unsaturated nitriles. This method tolerates aliphatic and aromatic alkenes substituted with a variety of functional groups such...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694676/ https://www.ncbi.nlm.nih.gov/pubmed/35423113 http://dx.doi.org/10.1039/d0ra10693c |
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author | Ahmad, Muhammad Siddique Ahmad, Atique |
author_facet | Ahmad, Muhammad Siddique Ahmad, Atique |
author_sort | Ahmad, Muhammad Siddique |
collection | PubMed |
description | We describe copper-catalyzed cyanomethylation of imines and α,β-alkenes with a methylnitrile source and provide an efficient route to synthesize arylacrylonitriles and β,γ-unsaturated nitriles. This method tolerates aliphatic and aromatic alkenes substituted with a variety of functional groups such as F, Cl, Br, Me, OMe, tert-Bu, NO(2), NH(2) and CO(2)H with good to excellent yields (69–98%). These systems consist of inexpensive, simple copper catalyst and acetonitrile with its derivatives (α-bromo/α-iodo-acetonitrile) and are highly applicable in the industrial production of acrylonitriles. |
format | Online Article Text |
id | pubmed-8694676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86946762022-04-13 Cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives Ahmad, Muhammad Siddique Ahmad, Atique RSC Adv Chemistry We describe copper-catalyzed cyanomethylation of imines and α,β-alkenes with a methylnitrile source and provide an efficient route to synthesize arylacrylonitriles and β,γ-unsaturated nitriles. This method tolerates aliphatic and aromatic alkenes substituted with a variety of functional groups such as F, Cl, Br, Me, OMe, tert-Bu, NO(2), NH(2) and CO(2)H with good to excellent yields (69–98%). These systems consist of inexpensive, simple copper catalyst and acetonitrile with its derivatives (α-bromo/α-iodo-acetonitrile) and are highly applicable in the industrial production of acrylonitriles. The Royal Society of Chemistry 2021-01-28 /pmc/articles/PMC8694676/ /pubmed/35423113 http://dx.doi.org/10.1039/d0ra10693c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Ahmad, Muhammad Siddique Ahmad, Atique Cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives |
title | Cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives |
title_full | Cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives |
title_fullStr | Cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives |
title_full_unstemmed | Cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives |
title_short | Cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives |
title_sort | cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694676/ https://www.ncbi.nlm.nih.gov/pubmed/35423113 http://dx.doi.org/10.1039/d0ra10693c |
work_keys_str_mv | AT ahmadmuhammadsiddique cucatalyzedcyanomethylationofiminesandabalkeneswithacetonitrileanditsderivatives AT ahmadatique cucatalyzedcyanomethylationofiminesandabalkeneswithacetonitrileanditsderivatives |