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Controlling Chemoselectivity of Catalytic Hydroboration with Light

The ability to selectively react one functional group in the presence of another underpins efficient reaction sequences. Despite many designer catalytic systems being reported for hydroboration reactions, which allow introduction of a functional handle for cross‐coupling or act as mild method for re...

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Autores principales: Bergamaschi, Enrico, Lunic, Danijela, McLean, Liam A., Hohenadel, Melissa, Chen, Yi‐Kai, Teskey, Christopher J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305532/
https://www.ncbi.nlm.nih.gov/pubmed/34905284
http://dx.doi.org/10.1002/anie.202114482
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author Bergamaschi, Enrico
Lunic, Danijela
McLean, Liam A.
Hohenadel, Melissa
Chen, Yi‐Kai
Teskey, Christopher J.
author_facet Bergamaschi, Enrico
Lunic, Danijela
McLean, Liam A.
Hohenadel, Melissa
Chen, Yi‐Kai
Teskey, Christopher J.
author_sort Bergamaschi, Enrico
collection PubMed
description The ability to selectively react one functional group in the presence of another underpins efficient reaction sequences. Despite many designer catalytic systems being reported for hydroboration reactions, which allow introduction of a functional handle for cross‐coupling or act as mild method for reducing polar functionality, these platforms rarely deal with more complex systems where multiple potentially reactive sites exist. Here we demonstrate, for the first time, the ability to use light to distinguish between ketones and carboxylic acids in more complex molecules. By taking advantage of different activation modes, a single catalytic system can be used for hydroboration, with the chemoselectivity dictated only by the presence or absence of visible light.
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spelling pubmed-93055322022-07-28 Controlling Chemoselectivity of Catalytic Hydroboration with Light Bergamaschi, Enrico Lunic, Danijela McLean, Liam A. Hohenadel, Melissa Chen, Yi‐Kai Teskey, Christopher J. Angew Chem Int Ed Engl Communications The ability to selectively react one functional group in the presence of another underpins efficient reaction sequences. Despite many designer catalytic systems being reported for hydroboration reactions, which allow introduction of a functional handle for cross‐coupling or act as mild method for reducing polar functionality, these platforms rarely deal with more complex systems where multiple potentially reactive sites exist. Here we demonstrate, for the first time, the ability to use light to distinguish between ketones and carboxylic acids in more complex molecules. By taking advantage of different activation modes, a single catalytic system can be used for hydroboration, with the chemoselectivity dictated only by the presence or absence of visible light. John Wiley and Sons Inc. 2022-01-11 2022-02-14 /pmc/articles/PMC9305532/ /pubmed/34905284 http://dx.doi.org/10.1002/anie.202114482 Text en © 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Bergamaschi, Enrico
Lunic, Danijela
McLean, Liam A.
Hohenadel, Melissa
Chen, Yi‐Kai
Teskey, Christopher J.
Controlling Chemoselectivity of Catalytic Hydroboration with Light
title Controlling Chemoselectivity of Catalytic Hydroboration with Light
title_full Controlling Chemoselectivity of Catalytic Hydroboration with Light
title_fullStr Controlling Chemoselectivity of Catalytic Hydroboration with Light
title_full_unstemmed Controlling Chemoselectivity of Catalytic Hydroboration with Light
title_short Controlling Chemoselectivity of Catalytic Hydroboration with Light
title_sort controlling chemoselectivity of catalytic hydroboration with light
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305532/
https://www.ncbi.nlm.nih.gov/pubmed/34905284
http://dx.doi.org/10.1002/anie.202114482
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