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Multicomponent syntheses of 5- and 6-membered aromatic heterocycles using group 4–8 transition metal catalysts

In this Perspective, we discuss recent syntheses of 5- and 6-membered aromatic heterocycles via multicomponent reactions (MCRs) that are catalyzed by group 4–8 transition metals. These MCRs can be categorized based on the substrate components used to generate the cyclized product, as well as on comm...

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Autores principales: Huh, Daniel N., Cheng, Yukun, Frye, Connor W., Egger, Dominic T., Tonks, Ian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293814/
https://www.ncbi.nlm.nih.gov/pubmed/34349931
http://dx.doi.org/10.1039/d1sc03037j
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author Huh, Daniel N.
Cheng, Yukun
Frye, Connor W.
Egger, Dominic T.
Tonks, Ian A.
author_facet Huh, Daniel N.
Cheng, Yukun
Frye, Connor W.
Egger, Dominic T.
Tonks, Ian A.
author_sort Huh, Daniel N.
collection PubMed
description In this Perspective, we discuss recent syntheses of 5- and 6-membered aromatic heterocycles via multicomponent reactions (MCRs) that are catalyzed by group 4–8 transition metals. These MCRs can be categorized based on the substrate components used to generate the cyclized product, as well as on common mechanistic features between the catalyst systems. These particular groupings are intended to highlight mechanistic and strategic similarities between otherwise disparate transition metals and to encourage future work exploring related systems with otherwise-overlooked elements. Importantly, in many cases these early- to mid-transition metal catalysts have been shown to be as effective for heterocycle syntheses as the later (and more commonly implemented) group 9–11 metals.
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spelling pubmed-82938142021-08-03 Multicomponent syntheses of 5- and 6-membered aromatic heterocycles using group 4–8 transition metal catalysts Huh, Daniel N. Cheng, Yukun Frye, Connor W. Egger, Dominic T. Tonks, Ian A. Chem Sci Chemistry In this Perspective, we discuss recent syntheses of 5- and 6-membered aromatic heterocycles via multicomponent reactions (MCRs) that are catalyzed by group 4–8 transition metals. These MCRs can be categorized based on the substrate components used to generate the cyclized product, as well as on common mechanistic features between the catalyst systems. These particular groupings are intended to highlight mechanistic and strategic similarities between otherwise disparate transition metals and to encourage future work exploring related systems with otherwise-overlooked elements. Importantly, in many cases these early- to mid-transition metal catalysts have been shown to be as effective for heterocycle syntheses as the later (and more commonly implemented) group 9–11 metals. The Royal Society of Chemistry 2021-06-29 /pmc/articles/PMC8293814/ /pubmed/34349931 http://dx.doi.org/10.1039/d1sc03037j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Huh, Daniel N.
Cheng, Yukun
Frye, Connor W.
Egger, Dominic T.
Tonks, Ian A.
Multicomponent syntheses of 5- and 6-membered aromatic heterocycles using group 4–8 transition metal catalysts
title Multicomponent syntheses of 5- and 6-membered aromatic heterocycles using group 4–8 transition metal catalysts
title_full Multicomponent syntheses of 5- and 6-membered aromatic heterocycles using group 4–8 transition metal catalysts
title_fullStr Multicomponent syntheses of 5- and 6-membered aromatic heterocycles using group 4–8 transition metal catalysts
title_full_unstemmed Multicomponent syntheses of 5- and 6-membered aromatic heterocycles using group 4–8 transition metal catalysts
title_short Multicomponent syntheses of 5- and 6-membered aromatic heterocycles using group 4–8 transition metal catalysts
title_sort multicomponent syntheses of 5- and 6-membered aromatic heterocycles using group 4–8 transition metal catalysts
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293814/
https://www.ncbi.nlm.nih.gov/pubmed/34349931
http://dx.doi.org/10.1039/d1sc03037j
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