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Rational Design of a Second Generation Catalyst for Preparation of Allylsilanes Using the Silyl-Heck Reaction

[Image: see text] Using rational ligand design, we have developed of a second-generation ligand, bis(3,5-di-tert-butylphenyl)(tert-butyl)phosphine, for the preparation of allylsilanes using the palladium-catalyzed silyl-Heck reaction. This new ligand provides nearly complete suppression of starting...

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Autores principales: McAtee, Jesse R., Yap, Glenn P. A., Watson, Donald A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105080/
https://www.ncbi.nlm.nih.gov/pubmed/25003502
http://dx.doi.org/10.1021/ja505446y
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author McAtee, Jesse R.
Yap, Glenn P. A.
Watson, Donald A.
author_facet McAtee, Jesse R.
Yap, Glenn P. A.
Watson, Donald A.
author_sort McAtee, Jesse R.
collection PubMed
description [Image: see text] Using rational ligand design, we have developed of a second-generation ligand, bis(3,5-di-tert-butylphenyl)(tert-butyl)phosphine, for the preparation of allylsilanes using the palladium-catalyzed silyl-Heck reaction. This new ligand provides nearly complete suppression of starting material alkene isomerization that was observed with our first-generation catalyst, providing vastly improved yields of allylsilanes from simple alkene starting materials. The studies quantifying the electronic and steric properties of the new ligand are described. Finally, we report an X-ray crystal structure of a palladium complex resulting from the oxidative addition of Me(3)SiI using an analogous ligand that provides significant insight into the nature of the catalytic system.
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spelling pubmed-41050802015-07-08 Rational Design of a Second Generation Catalyst for Preparation of Allylsilanes Using the Silyl-Heck Reaction McAtee, Jesse R. Yap, Glenn P. A. Watson, Donald A. J Am Chem Soc [Image: see text] Using rational ligand design, we have developed of a second-generation ligand, bis(3,5-di-tert-butylphenyl)(tert-butyl)phosphine, for the preparation of allylsilanes using the palladium-catalyzed silyl-Heck reaction. This new ligand provides nearly complete suppression of starting material alkene isomerization that was observed with our first-generation catalyst, providing vastly improved yields of allylsilanes from simple alkene starting materials. The studies quantifying the electronic and steric properties of the new ligand are described. Finally, we report an X-ray crystal structure of a palladium complex resulting from the oxidative addition of Me(3)SiI using an analogous ligand that provides significant insight into the nature of the catalytic system. American Chemical Society 2014-07-08 2014-07-16 /pmc/articles/PMC4105080/ /pubmed/25003502 http://dx.doi.org/10.1021/ja505446y Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle McAtee, Jesse R.
Yap, Glenn P. A.
Watson, Donald A.
Rational Design of a Second Generation Catalyst for Preparation of Allylsilanes Using the Silyl-Heck Reaction
title Rational Design of a Second Generation Catalyst for Preparation of Allylsilanes Using the Silyl-Heck Reaction
title_full Rational Design of a Second Generation Catalyst for Preparation of Allylsilanes Using the Silyl-Heck Reaction
title_fullStr Rational Design of a Second Generation Catalyst for Preparation of Allylsilanes Using the Silyl-Heck Reaction
title_full_unstemmed Rational Design of a Second Generation Catalyst for Preparation of Allylsilanes Using the Silyl-Heck Reaction
title_short Rational Design of a Second Generation Catalyst for Preparation of Allylsilanes Using the Silyl-Heck Reaction
title_sort rational design of a second generation catalyst for preparation of allylsilanes using the silyl-heck reaction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105080/
https://www.ncbi.nlm.nih.gov/pubmed/25003502
http://dx.doi.org/10.1021/ja505446y
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