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Group 13 exchange and transborylation in catalysis

Catalysis is dominated by the use of rare and potentially toxic transition metals. The main group offers a potentially sustainable alternative for catalysis, due to the generally higher abundance and lower toxicity of these elements. Group 13 elements have a rich catalogue of stoichiometric addition...

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Autores principales: Willcox, Dominic R, Thomas, Stephen P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043741/
https://www.ncbi.nlm.nih.gov/pubmed/36998308
http://dx.doi.org/10.3762/bjoc.19.28
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author Willcox, Dominic R
Thomas, Stephen P
author_facet Willcox, Dominic R
Thomas, Stephen P
author_sort Willcox, Dominic R
collection PubMed
description Catalysis is dominated by the use of rare and potentially toxic transition metals. The main group offers a potentially sustainable alternative for catalysis, due to the generally higher abundance and lower toxicity of these elements. Group 13 elements have a rich catalogue of stoichiometric addition reactions to unsaturated bonds but cannot undergo the redox chemistry which underpins transition-metal catalysis. Group 13 exchange reactions transfer one or more groups from one group 13 element to another, through σ-bond metathesis; where boron is both of the group 13 elements, this is termed transborylation. These redox-neutral processes are increasingly being used to render traditionally stoichiometric group 13-mediated processes catalytic and develop new catalytic processes, examples of which are the focus of this review.
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spelling pubmed-100437412023-03-29 Group 13 exchange and transborylation in catalysis Willcox, Dominic R Thomas, Stephen P Beilstein J Org Chem Review Catalysis is dominated by the use of rare and potentially toxic transition metals. The main group offers a potentially sustainable alternative for catalysis, due to the generally higher abundance and lower toxicity of these elements. Group 13 elements have a rich catalogue of stoichiometric addition reactions to unsaturated bonds but cannot undergo the redox chemistry which underpins transition-metal catalysis. Group 13 exchange reactions transfer one or more groups from one group 13 element to another, through σ-bond metathesis; where boron is both of the group 13 elements, this is termed transborylation. These redox-neutral processes are increasingly being used to render traditionally stoichiometric group 13-mediated processes catalytic and develop new catalytic processes, examples of which are the focus of this review. Beilstein-Institut 2023-03-21 /pmc/articles/PMC10043741/ /pubmed/36998308 http://dx.doi.org/10.3762/bjoc.19.28 Text en Copyright © 2023, Willcox and Thomas https://creativecommons.org/licenses/by/4.0/This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material.
spellingShingle Review
Willcox, Dominic R
Thomas, Stephen P
Group 13 exchange and transborylation in catalysis
title Group 13 exchange and transborylation in catalysis
title_full Group 13 exchange and transborylation in catalysis
title_fullStr Group 13 exchange and transborylation in catalysis
title_full_unstemmed Group 13 exchange and transborylation in catalysis
title_short Group 13 exchange and transborylation in catalysis
title_sort group 13 exchange and transborylation in catalysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043741/
https://www.ncbi.nlm.nih.gov/pubmed/36998308
http://dx.doi.org/10.3762/bjoc.19.28
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