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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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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. |
format | Online Article Text |
id | pubmed-4105080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
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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