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Ag(I)–C–H Activation Enables Near-Room-Temperature Direct α-Arylation of Benzo[b]thiophenes
[Image: see text] The first example of near-room-temperature α-arylation of benzo[b]thiophenes is reported. The discovery rests on the observation of a switch in α-/β-regioselectivity at different loadings of Pd(2)(dba)(3)·CHCl(3) in the coupling between benzo[b]thiophene and 4-iodotoluene. We show...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370252/ https://www.ncbi.nlm.nih.gov/pubmed/29983049 http://dx.doi.org/10.1021/jacs.8b05361 |
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author | Colletto, Chiara Panigrahi, Adyasha Fernández-Casado, Jaime Larrosa, Igor |
author_facet | Colletto, Chiara Panigrahi, Adyasha Fernández-Casado, Jaime Larrosa, Igor |
author_sort | Colletto, Chiara |
collection | PubMed |
description | [Image: see text] The first example of near-room-temperature α-arylation of benzo[b]thiophenes is reported. The discovery rests on the observation of a switch in α-/β-regioselectivity at different loadings of Pd(2)(dba)(3)·CHCl(3) in the coupling between benzo[b]thiophene and 4-iodotoluene. We show that this unprecedented regioselectivity switch is driven by a Ag(I)-mediated C–H activation at the α-C–H position, which becomes the dominant mode of reactivity at low concentrations of Pd. Competition experiments, kinetic studies, KIE, and D/H scrambling experiments have been carried out supporting this mechanism. |
format | Online Article Text |
id | pubmed-6370252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-63702522019-02-14 Ag(I)–C–H Activation Enables Near-Room-Temperature Direct α-Arylation of Benzo[b]thiophenes Colletto, Chiara Panigrahi, Adyasha Fernández-Casado, Jaime Larrosa, Igor J Am Chem Soc [Image: see text] The first example of near-room-temperature α-arylation of benzo[b]thiophenes is reported. The discovery rests on the observation of a switch in α-/β-regioselectivity at different loadings of Pd(2)(dba)(3)·CHCl(3) in the coupling between benzo[b]thiophene and 4-iodotoluene. We show that this unprecedented regioselectivity switch is driven by a Ag(I)-mediated C–H activation at the α-C–H position, which becomes the dominant mode of reactivity at low concentrations of Pd. Competition experiments, kinetic studies, KIE, and D/H scrambling experiments have been carried out supporting this mechanism. American Chemical Society 2018-07-09 2018-08-01 /pmc/articles/PMC6370252/ /pubmed/29983049 http://dx.doi.org/10.1021/jacs.8b05361 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Colletto, Chiara Panigrahi, Adyasha Fernández-Casado, Jaime Larrosa, Igor Ag(I)–C–H Activation Enables Near-Room-Temperature Direct α-Arylation of Benzo[b]thiophenes |
title | Ag(I)–C–H
Activation Enables Near-Room-Temperature
Direct α-Arylation of Benzo[b]thiophenes |
title_full | Ag(I)–C–H
Activation Enables Near-Room-Temperature
Direct α-Arylation of Benzo[b]thiophenes |
title_fullStr | Ag(I)–C–H
Activation Enables Near-Room-Temperature
Direct α-Arylation of Benzo[b]thiophenes |
title_full_unstemmed | Ag(I)–C–H
Activation Enables Near-Room-Temperature
Direct α-Arylation of Benzo[b]thiophenes |
title_short | Ag(I)–C–H
Activation Enables Near-Room-Temperature
Direct α-Arylation of Benzo[b]thiophenes |
title_sort | ag(i)–c–h
activation enables near-room-temperature
direct α-arylation of benzo[b]thiophenes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370252/ https://www.ncbi.nlm.nih.gov/pubmed/29983049 http://dx.doi.org/10.1021/jacs.8b05361 |
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