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Radical‐Induced 1,2‐Migrations of Boron Ate Complexes
1,2‐Boron ate rearrangements represent a fundamental class of transformations to establish new C−C bonds while retaining the valuable boron moiety in the product. In established ionic processes, the boron ate complex is activated by an external electrophile to induce a 1,2‐migration from boron to an...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7319355/ https://www.ncbi.nlm.nih.gov/pubmed/32612487 http://dx.doi.org/10.1002/adsc.201901503 |
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author | Kischkewitz, Marvin Friese, Florian W. Studer, Armido |
author_facet | Kischkewitz, Marvin Friese, Florian W. Studer, Armido |
author_sort | Kischkewitz, Marvin |
collection | PubMed |
description | 1,2‐Boron ate rearrangements represent a fundamental class of transformations to establish new C−C bonds while retaining the valuable boron moiety in the product. In established ionic processes, the boron ate complex is activated by an external electrophile to induce a 1,2‐migration from boron to an adjacent sp (3) or sp (2) carbon atom. Recently, two complementary radical polar crossover approaches have been explored for both classes, 1,2‐migrations to sp (2) and sp (3) carbon centers. This review describes the general concepts in this emerging research field and summarizes recent developments of radical‐induced 1,2‐migrations from boron to carbon. [Image: see text] |
format | Online Article Text |
id | pubmed-7319355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73193552020-06-29 Radical‐Induced 1,2‐Migrations of Boron Ate Complexes Kischkewitz, Marvin Friese, Florian W. Studer, Armido Adv Synth Catal Reviews 1,2‐Boron ate rearrangements represent a fundamental class of transformations to establish new C−C bonds while retaining the valuable boron moiety in the product. In established ionic processes, the boron ate complex is activated by an external electrophile to induce a 1,2‐migration from boron to an adjacent sp (3) or sp (2) carbon atom. Recently, two complementary radical polar crossover approaches have been explored for both classes, 1,2‐migrations to sp (2) and sp (3) carbon centers. This review describes the general concepts in this emerging research field and summarizes recent developments of radical‐induced 1,2‐migrations from boron to carbon. [Image: see text] John Wiley and Sons Inc. 2020-02-21 2020-05-26 /pmc/articles/PMC7319355/ /pubmed/32612487 http://dx.doi.org/10.1002/adsc.201901503 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Kischkewitz, Marvin Friese, Florian W. Studer, Armido Radical‐Induced 1,2‐Migrations of Boron Ate Complexes |
title | Radical‐Induced 1,2‐Migrations of Boron Ate Complexes |
title_full | Radical‐Induced 1,2‐Migrations of Boron Ate Complexes |
title_fullStr | Radical‐Induced 1,2‐Migrations of Boron Ate Complexes |
title_full_unstemmed | Radical‐Induced 1,2‐Migrations of Boron Ate Complexes |
title_short | Radical‐Induced 1,2‐Migrations of Boron Ate Complexes |
title_sort | radical‐induced 1,2‐migrations of boron ate complexes |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7319355/ https://www.ncbi.nlm.nih.gov/pubmed/32612487 http://dx.doi.org/10.1002/adsc.201901503 |
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