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Enantioselective Rhodium‐Catalyzed Coupling of Arylboronic Acids, 1,3‐Enynes, and Imines by Alkenyl‐to‐Allyl 1,4‐Rhodium(I) Migration
A chiral rhodium complex catalyzes the highly enantioselective coupling of arylboronic acids, 1,3‐enynes, and imines to give homoallylic sulfamates. The key step is the generation of allylrhodium(I) species by alkenyl‐to‐allyl 1,4‐rhodium(I) migration.
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765452/ https://www.ncbi.nlm.nih.gov/pubmed/28980437 http://dx.doi.org/10.1002/anie.201709334 |
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author | Callingham, Michael Partridge, Benjamin M. Lewis, William Lam, Hon Wai |
author_facet | Callingham, Michael Partridge, Benjamin M. Lewis, William Lam, Hon Wai |
author_sort | Callingham, Michael |
collection | PubMed |
description | A chiral rhodium complex catalyzes the highly enantioselective coupling of arylboronic acids, 1,3‐enynes, and imines to give homoallylic sulfamates. The key step is the generation of allylrhodium(I) species by alkenyl‐to‐allyl 1,4‐rhodium(I) migration. |
format | Online Article Text |
id | pubmed-5765452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57654522018-02-01 Enantioselective Rhodium‐Catalyzed Coupling of Arylboronic Acids, 1,3‐Enynes, and Imines by Alkenyl‐to‐Allyl 1,4‐Rhodium(I) Migration Callingham, Michael Partridge, Benjamin M. Lewis, William Lam, Hon Wai Angew Chem Int Ed Engl Communications A chiral rhodium complex catalyzes the highly enantioselective coupling of arylboronic acids, 1,3‐enynes, and imines to give homoallylic sulfamates. The key step is the generation of allylrhodium(I) species by alkenyl‐to‐allyl 1,4‐rhodium(I) migration. John Wiley and Sons Inc. 2017-11-24 2017-12-18 /pmc/articles/PMC5765452/ /pubmed/28980437 http://dx.doi.org/10.1002/anie.201709334 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (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 | Communications Callingham, Michael Partridge, Benjamin M. Lewis, William Lam, Hon Wai Enantioselective Rhodium‐Catalyzed Coupling of Arylboronic Acids, 1,3‐Enynes, and Imines by Alkenyl‐to‐Allyl 1,4‐Rhodium(I) Migration |
title | Enantioselective Rhodium‐Catalyzed Coupling of Arylboronic Acids, 1,3‐Enynes, and Imines by Alkenyl‐to‐Allyl 1,4‐Rhodium(I) Migration |
title_full | Enantioselective Rhodium‐Catalyzed Coupling of Arylboronic Acids, 1,3‐Enynes, and Imines by Alkenyl‐to‐Allyl 1,4‐Rhodium(I) Migration |
title_fullStr | Enantioselective Rhodium‐Catalyzed Coupling of Arylboronic Acids, 1,3‐Enynes, and Imines by Alkenyl‐to‐Allyl 1,4‐Rhodium(I) Migration |
title_full_unstemmed | Enantioselective Rhodium‐Catalyzed Coupling of Arylboronic Acids, 1,3‐Enynes, and Imines by Alkenyl‐to‐Allyl 1,4‐Rhodium(I) Migration |
title_short | Enantioselective Rhodium‐Catalyzed Coupling of Arylboronic Acids, 1,3‐Enynes, and Imines by Alkenyl‐to‐Allyl 1,4‐Rhodium(I) Migration |
title_sort | enantioselective rhodium‐catalyzed coupling of arylboronic acids, 1,3‐enynes, and imines by alkenyl‐to‐allyl 1,4‐rhodium(i) migration |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765452/ https://www.ncbi.nlm.nih.gov/pubmed/28980437 http://dx.doi.org/10.1002/anie.201709334 |
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