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Boron-Catalyzed, Diastereo- and Enantioselective Allylation of Ketones with Allenes
[Image: see text] The diastereo- and enantioselective allylation of ketones remains a synthetic challenge, with transition metal catalysis offering the most applied methods. Here, a boron-catalyzed allylation of ketones with allenes is presented. Excellent yield, regioselectivity, and diastereoselec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442582/ https://www.ncbi.nlm.nih.gov/pubmed/36082052 http://dx.doi.org/10.1021/acscatal.2c03158 |
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author | Nicholson, Kieran Peng, Yuxuan Llopis, Natalia Willcox, Dominic R. Nichol, Gary S. Langer, Thomas Baeza, Alejandro Thomas, Stephen P. |
author_facet | Nicholson, Kieran Peng, Yuxuan Llopis, Natalia Willcox, Dominic R. Nichol, Gary S. Langer, Thomas Baeza, Alejandro Thomas, Stephen P. |
author_sort | Nicholson, Kieran |
collection | PubMed |
description | [Image: see text] The diastereo- and enantioselective allylation of ketones remains a synthetic challenge, with transition metal catalysis offering the most applied methods. Here, a boron-catalyzed allylation of ketones with allenes is presented. Excellent yield, regioselectivity, and diastereoselectivity were found across functionalized substrates. The reaction was further developed to accommodate an enantioenriched boron catalyst and thus gave asymmetric ketone allylation in good yield, diastereoselectivity, and enantioselectivity. Mechanistic studies supported a hydroboration–allylation–transborylation pathway. |
format | Online Article Text |
id | pubmed-9442582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94425822022-09-06 Boron-Catalyzed, Diastereo- and Enantioselective Allylation of Ketones with Allenes Nicholson, Kieran Peng, Yuxuan Llopis, Natalia Willcox, Dominic R. Nichol, Gary S. Langer, Thomas Baeza, Alejandro Thomas, Stephen P. ACS Catal [Image: see text] The diastereo- and enantioselective allylation of ketones remains a synthetic challenge, with transition metal catalysis offering the most applied methods. Here, a boron-catalyzed allylation of ketones with allenes is presented. Excellent yield, regioselectivity, and diastereoselectivity were found across functionalized substrates. The reaction was further developed to accommodate an enantioenriched boron catalyst and thus gave asymmetric ketone allylation in good yield, diastereoselectivity, and enantioselectivity. Mechanistic studies supported a hydroboration–allylation–transborylation pathway. American Chemical Society 2022-08-22 2022-09-02 /pmc/articles/PMC9442582/ /pubmed/36082052 http://dx.doi.org/10.1021/acscatal.2c03158 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Nicholson, Kieran Peng, Yuxuan Llopis, Natalia Willcox, Dominic R. Nichol, Gary S. Langer, Thomas Baeza, Alejandro Thomas, Stephen P. Boron-Catalyzed, Diastereo- and Enantioselective Allylation of Ketones with Allenes |
title | Boron-Catalyzed,
Diastereo- and Enantioselective Allylation
of Ketones with Allenes |
title_full | Boron-Catalyzed,
Diastereo- and Enantioselective Allylation
of Ketones with Allenes |
title_fullStr | Boron-Catalyzed,
Diastereo- and Enantioselective Allylation
of Ketones with Allenes |
title_full_unstemmed | Boron-Catalyzed,
Diastereo- and Enantioselective Allylation
of Ketones with Allenes |
title_short | Boron-Catalyzed,
Diastereo- and Enantioselective Allylation
of Ketones with Allenes |
title_sort | boron-catalyzed,
diastereo- and enantioselective allylation
of ketones with allenes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442582/ https://www.ncbi.nlm.nih.gov/pubmed/36082052 http://dx.doi.org/10.1021/acscatal.2c03158 |
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