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Cp*Co(III)-Catalyzed C–H Hydroarylation of Alkynes and Alkenes and Beyond: A Versatile Synthetic Tool

[Image: see text] The use of earth-abundant first-row transition metals, such as cobalt, in C–H activation reactions for the construction and functionalization of a wide variety of structures has become a central topic in synthetic chemistry over the last few years. In this context, the emergence of...

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Autores principales: Carral-Menoyo, Asier, Sotomayor, Nuria, Lete, Esther
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542607/
https://www.ncbi.nlm.nih.gov/pubmed/33043175
http://dx.doi.org/10.1021/acsomega.0c03639
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author Carral-Menoyo, Asier
Sotomayor, Nuria
Lete, Esther
author_facet Carral-Menoyo, Asier
Sotomayor, Nuria
Lete, Esther
author_sort Carral-Menoyo, Asier
collection PubMed
description [Image: see text] The use of earth-abundant first-row transition metals, such as cobalt, in C–H activation reactions for the construction and functionalization of a wide variety of structures has become a central topic in synthetic chemistry over the last few years. In this context, the emergence of cobalt catalysts bearing pentamethylcyclopentadienyl ligands (Cp*) has had a major impact on the development of synthetic methodologies. Cp*Co(III) complexes have been proven to possess unique reactivity compared, for example, to their Rh(III) counterparts, obtaining improved chemo- or regioselectivities, as well as yielding new reactivities. This perspective is focused on recent advances on the alkylation and alkenylation reactions of (hetero)arenes with alkenes and alkynes under Cp*Co(III) catalysis.
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spelling pubmed-75426072020-10-09 Cp*Co(III)-Catalyzed C–H Hydroarylation of Alkynes and Alkenes and Beyond: A Versatile Synthetic Tool Carral-Menoyo, Asier Sotomayor, Nuria Lete, Esther ACS Omega [Image: see text] The use of earth-abundant first-row transition metals, such as cobalt, in C–H activation reactions for the construction and functionalization of a wide variety of structures has become a central topic in synthetic chemistry over the last few years. In this context, the emergence of cobalt catalysts bearing pentamethylcyclopentadienyl ligands (Cp*) has had a major impact on the development of synthetic methodologies. Cp*Co(III) complexes have been proven to possess unique reactivity compared, for example, to their Rh(III) counterparts, obtaining improved chemo- or regioselectivities, as well as yielding new reactivities. This perspective is focused on recent advances on the alkylation and alkenylation reactions of (hetero)arenes with alkenes and alkynes under Cp*Co(III) catalysis. American Chemical Society 2020-09-15 /pmc/articles/PMC7542607/ /pubmed/33043175 http://dx.doi.org/10.1021/acsomega.0c03639 Text en This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Carral-Menoyo, Asier
Sotomayor, Nuria
Lete, Esther
Cp*Co(III)-Catalyzed C–H Hydroarylation of Alkynes and Alkenes and Beyond: A Versatile Synthetic Tool
title Cp*Co(III)-Catalyzed C–H Hydroarylation of Alkynes and Alkenes and Beyond: A Versatile Synthetic Tool
title_full Cp*Co(III)-Catalyzed C–H Hydroarylation of Alkynes and Alkenes and Beyond: A Versatile Synthetic Tool
title_fullStr Cp*Co(III)-Catalyzed C–H Hydroarylation of Alkynes and Alkenes and Beyond: A Versatile Synthetic Tool
title_full_unstemmed Cp*Co(III)-Catalyzed C–H Hydroarylation of Alkynes and Alkenes and Beyond: A Versatile Synthetic Tool
title_short Cp*Co(III)-Catalyzed C–H Hydroarylation of Alkynes and Alkenes and Beyond: A Versatile Synthetic Tool
title_sort cp*co(iii)-catalyzed c–h hydroarylation of alkynes and alkenes and beyond: a versatile synthetic tool
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542607/
https://www.ncbi.nlm.nih.gov/pubmed/33043175
http://dx.doi.org/10.1021/acsomega.0c03639
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