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Regioselective Hydroacylation of 1,3-Dienes by Cobalt Catalysis
[Image: see text] We describe a cobalt-catalyzed hydroacylation of 1,3-dienes with non-chelating aldehydes. Aromatic aldehydes provide 1,4-addition products as the major isomer, while aliphatic aldehydes favor 1,2-hydroacylation products. The kinetic profile supports an oxidative cyclization mechani...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117386/ https://www.ncbi.nlm.nih.gov/pubmed/24588202 http://dx.doi.org/10.1021/ja500268w |
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author | Chen, Qing-An Kim, Daniel K. Dong, Vy M. |
author_facet | Chen, Qing-An Kim, Daniel K. Dong, Vy M. |
author_sort | Chen, Qing-An |
collection | PubMed |
description | [Image: see text] We describe a cobalt-catalyzed hydroacylation of 1,3-dienes with non-chelating aldehydes. Aromatic aldehydes provide 1,4-addition products as the major isomer, while aliphatic aldehydes favor 1,2-hydroacylation products. The kinetic profile supports an oxidative cyclization mechanism involving a cobaltacycle intermediate that undergoes transformation with high regio- and stereoselectivity. |
format | Online Article Text |
id | pubmed-4117386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-41173862015-03-03 Regioselective Hydroacylation of 1,3-Dienes by Cobalt Catalysis Chen, Qing-An Kim, Daniel K. Dong, Vy M. J Am Chem Soc [Image: see text] We describe a cobalt-catalyzed hydroacylation of 1,3-dienes with non-chelating aldehydes. Aromatic aldehydes provide 1,4-addition products as the major isomer, while aliphatic aldehydes favor 1,2-hydroacylation products. The kinetic profile supports an oxidative cyclization mechanism involving a cobaltacycle intermediate that undergoes transformation with high regio- and stereoselectivity. American Chemical Society 2014-03-03 2014-03-12 /pmc/articles/PMC4117386/ /pubmed/24588202 http://dx.doi.org/10.1021/ja500268w Text en Copyright © 2014 American Chemical Society |
spellingShingle | Chen, Qing-An Kim, Daniel K. Dong, Vy M. Regioselective Hydroacylation of 1,3-Dienes by Cobalt Catalysis |
title | Regioselective
Hydroacylation of 1,3-Dienes by Cobalt
Catalysis |
title_full | Regioselective
Hydroacylation of 1,3-Dienes by Cobalt
Catalysis |
title_fullStr | Regioselective
Hydroacylation of 1,3-Dienes by Cobalt
Catalysis |
title_full_unstemmed | Regioselective
Hydroacylation of 1,3-Dienes by Cobalt
Catalysis |
title_short | Regioselective
Hydroacylation of 1,3-Dienes by Cobalt
Catalysis |
title_sort | regioselective
hydroacylation of 1,3-dienes by cobalt
catalysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117386/ https://www.ncbi.nlm.nih.gov/pubmed/24588202 http://dx.doi.org/10.1021/ja500268w |
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