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Asymmetric Hydroarylation of Vinylarenes Using a Synergistic Combination of CuH and Pd Catalysis
[Image: see text] Detailed in this Communication is the enantioselective synthesis of 1,1-diarylalkanes, a structure found in a range of pharmaceutical drug agents and natural products, through the employment of copper(I) hydride and palladium catalysis. Judicious choice of ligand for both Cu and Pd...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010014/ https://www.ncbi.nlm.nih.gov/pubmed/27346525 http://dx.doi.org/10.1021/jacs.6b04566 |
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author | Friis, Stig D. Pirnot, Michael T. Buchwald, Stephen L. |
author_facet | Friis, Stig D. Pirnot, Michael T. Buchwald, Stephen L. |
author_sort | Friis, Stig D. |
collection | PubMed |
description | [Image: see text] Detailed in this Communication is the enantioselective synthesis of 1,1-diarylalkanes, a structure found in a range of pharmaceutical drug agents and natural products, through the employment of copper(I) hydride and palladium catalysis. Judicious choice of ligand for both Cu and Pd enabled this hydroarylation protocol to work for an extensive array of aryl bromides and styrenes, including β-substituted vinylarenes and six-membered heterocycles, under relatively mild conditions. |
format | Online Article Text |
id | pubmed-5010014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50100142017-06-27 Asymmetric Hydroarylation of Vinylarenes Using a Synergistic Combination of CuH and Pd Catalysis Friis, Stig D. Pirnot, Michael T. Buchwald, Stephen L. J Am Chem Soc [Image: see text] Detailed in this Communication is the enantioselective synthesis of 1,1-diarylalkanes, a structure found in a range of pharmaceutical drug agents and natural products, through the employment of copper(I) hydride and palladium catalysis. Judicious choice of ligand for both Cu and Pd enabled this hydroarylation protocol to work for an extensive array of aryl bromides and styrenes, including β-substituted vinylarenes and six-membered heterocycles, under relatively mild conditions. American Chemical Society 2016-06-27 2016-07-13 /pmc/articles/PMC5010014/ /pubmed/27346525 http://dx.doi.org/10.1021/jacs.6b04566 Text en Copyright © 2016 American Chemical Society 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 | Friis, Stig D. Pirnot, Michael T. Buchwald, Stephen L. Asymmetric Hydroarylation of Vinylarenes Using a Synergistic Combination of CuH and Pd Catalysis |
title | Asymmetric
Hydroarylation of Vinylarenes Using a Synergistic Combination of CuH
and Pd Catalysis |
title_full | Asymmetric
Hydroarylation of Vinylarenes Using a Synergistic Combination of CuH
and Pd Catalysis |
title_fullStr | Asymmetric
Hydroarylation of Vinylarenes Using a Synergistic Combination of CuH
and Pd Catalysis |
title_full_unstemmed | Asymmetric
Hydroarylation of Vinylarenes Using a Synergistic Combination of CuH
and Pd Catalysis |
title_short | Asymmetric
Hydroarylation of Vinylarenes Using a Synergistic Combination of CuH
and Pd Catalysis |
title_sort | asymmetric
hydroarylation of vinylarenes using a synergistic combination of cuh
and pd catalysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010014/ https://www.ncbi.nlm.nih.gov/pubmed/27346525 http://dx.doi.org/10.1021/jacs.6b04566 |
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