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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...

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Autores principales: Friis, Stig D., Pirnot, Michael T., Buchwald, Stephen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
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.
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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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