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Base-Free Photoredox/Nickel Dual-Catalytic Cross-Coupling of Ammonium Alkylsilicates

[Image: see text] Single-electron transmetalation is recognized as an enabling technology for the mild transfer of alkyl groups to transition metal catalysts in cross-coupling reactions. Hypercoordinate silicates represent a new and improved class of radical precursors because of their low oxidation...

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Autores principales: Jouffroy, Matthieu, Primer, David N., Molander, Gary A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854202/
https://www.ncbi.nlm.nih.gov/pubmed/26704168
http://dx.doi.org/10.1021/jacs.5b10963
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author Jouffroy, Matthieu
Primer, David N.
Molander, Gary A.
author_facet Jouffroy, Matthieu
Primer, David N.
Molander, Gary A.
author_sort Jouffroy, Matthieu
collection PubMed
description [Image: see text] Single-electron transmetalation is recognized as an enabling technology for the mild transfer of alkyl groups to transition metal catalysts in cross-coupling reactions. Hypercoordinate silicates represent a new and improved class of radical precursors because of their low oxidation potentials and the innocuous byproducts generated upon oxidation. Herein, we report the cross-coupling of secondary and primary ammonium alkylsilicates with (hetero)aryl bromides in good to excellent yields. The base-free conditions have exceptional protic group tolerance on both partners, permitting the cross-coupling of unprotected primary and secondary amines.
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spelling pubmed-48542022016-12-24 Base-Free Photoredox/Nickel Dual-Catalytic Cross-Coupling of Ammonium Alkylsilicates Jouffroy, Matthieu Primer, David N. Molander, Gary A. J Am Chem Soc [Image: see text] Single-electron transmetalation is recognized as an enabling technology for the mild transfer of alkyl groups to transition metal catalysts in cross-coupling reactions. Hypercoordinate silicates represent a new and improved class of radical precursors because of their low oxidation potentials and the innocuous byproducts generated upon oxidation. Herein, we report the cross-coupling of secondary and primary ammonium alkylsilicates with (hetero)aryl bromides in good to excellent yields. The base-free conditions have exceptional protic group tolerance on both partners, permitting the cross-coupling of unprotected primary and secondary amines. American Chemical Society 2015-12-24 2016-01-20 /pmc/articles/PMC4854202/ /pubmed/26704168 http://dx.doi.org/10.1021/jacs.5b10963 Text en Copyright © 2015 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 Jouffroy, Matthieu
Primer, David N.
Molander, Gary A.
Base-Free Photoredox/Nickel Dual-Catalytic Cross-Coupling of Ammonium Alkylsilicates
title Base-Free Photoredox/Nickel Dual-Catalytic Cross-Coupling of Ammonium Alkylsilicates
title_full Base-Free Photoredox/Nickel Dual-Catalytic Cross-Coupling of Ammonium Alkylsilicates
title_fullStr Base-Free Photoredox/Nickel Dual-Catalytic Cross-Coupling of Ammonium Alkylsilicates
title_full_unstemmed Base-Free Photoredox/Nickel Dual-Catalytic Cross-Coupling of Ammonium Alkylsilicates
title_short Base-Free Photoredox/Nickel Dual-Catalytic Cross-Coupling of Ammonium Alkylsilicates
title_sort base-free photoredox/nickel dual-catalytic cross-coupling of ammonium alkylsilicates
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854202/
https://www.ncbi.nlm.nih.gov/pubmed/26704168
http://dx.doi.org/10.1021/jacs.5b10963
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