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Template catalysis by manganese pincer complexes: oxa- and aza-Michael additions to unsaturated nitriles

Activation of C[triple bond, length as m-dash]N bonds by metal–ligand cooperation provides a new route for the functionalization of nitriles. Herein, we report the electrophilic activation of unsaturated nitriles by dearomatized manganese pincer complexes for the oxa- and aza-Michael addition reacti...

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Autores principales: Tang, Shan, Milstein, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855260/
https://www.ncbi.nlm.nih.gov/pubmed/31762979
http://dx.doi.org/10.1039/c9sc03269j
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author Tang, Shan
Milstein, David
author_facet Tang, Shan
Milstein, David
author_sort Tang, Shan
collection PubMed
description Activation of C[triple bond, length as m-dash]N bonds by metal–ligand cooperation provides a new route for the functionalization of nitriles. Herein, we report the electrophilic activation of unsaturated nitriles by dearomatized manganese pincer complexes for the oxa- and aza-Michael addition reactions under very mild and neutral conditions. Derivatives of acrylonitrile and allyl cyanide furnished the corresponding β-addition products by reacting with alcohols and amines. Mechanistically, the catalysis is mostly ligand based. Reaction of the dearomatized PNN–Mn complex with 2-pentenenitrile or 3-pentenenitrile furnished an enamido–Mn complex. The equilibrium between an enamido complex and a ketimido complex, and reversible C–C bond formation with the ligand are proposed to play central roles in the catalysis.
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spelling pubmed-68552602019-11-22 Template catalysis by manganese pincer complexes: oxa- and aza-Michael additions to unsaturated nitriles Tang, Shan Milstein, David Chem Sci Chemistry Activation of C[triple bond, length as m-dash]N bonds by metal–ligand cooperation provides a new route for the functionalization of nitriles. Herein, we report the electrophilic activation of unsaturated nitriles by dearomatized manganese pincer complexes for the oxa- and aza-Michael addition reactions under very mild and neutral conditions. Derivatives of acrylonitrile and allyl cyanide furnished the corresponding β-addition products by reacting with alcohols and amines. Mechanistically, the catalysis is mostly ligand based. Reaction of the dearomatized PNN–Mn complex with 2-pentenenitrile or 3-pentenenitrile furnished an enamido–Mn complex. The equilibrium between an enamido complex and a ketimido complex, and reversible C–C bond formation with the ligand are proposed to play central roles in the catalysis. Royal Society of Chemistry 2019-08-07 /pmc/articles/PMC6855260/ /pubmed/31762979 http://dx.doi.org/10.1039/c9sc03269j Text en This journal is © The Royal Society of Chemistry 2019 https://creativecommons.org/licenses/by-nc/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Tang, Shan
Milstein, David
Template catalysis by manganese pincer complexes: oxa- and aza-Michael additions to unsaturated nitriles
title Template catalysis by manganese pincer complexes: oxa- and aza-Michael additions to unsaturated nitriles
title_full Template catalysis by manganese pincer complexes: oxa- and aza-Michael additions to unsaturated nitriles
title_fullStr Template catalysis by manganese pincer complexes: oxa- and aza-Michael additions to unsaturated nitriles
title_full_unstemmed Template catalysis by manganese pincer complexes: oxa- and aza-Michael additions to unsaturated nitriles
title_short Template catalysis by manganese pincer complexes: oxa- and aza-Michael additions to unsaturated nitriles
title_sort template catalysis by manganese pincer complexes: oxa- and aza-michael additions to unsaturated nitriles
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855260/
https://www.ncbi.nlm.nih.gov/pubmed/31762979
http://dx.doi.org/10.1039/c9sc03269j
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