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Efficient Approach to Carbinol Derivatives through Palladium-Catalyzed Base-Free Addition of Aryltriolborates to Aldehydes

Palladium-catalyzed base-free addition of aryltriolborates to aldehydes has been developed, leading to a wide range of carbinol derivatives in good to excellent yields. The efficiency of this transformation was demonstrated by compatibility with a wide range of functional groups. The present synthet...

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Detalles Bibliográficos
Autores principales: Hu, Kun, Ye, Pengqing, Zhen, Qianqian, Yao, Xinrong, Xu, Tong, Shao, Yinlin, Chen, Jiuxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151780/
https://www.ncbi.nlm.nih.gov/pubmed/28930180
http://dx.doi.org/10.3390/molecules22091580
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author Hu, Kun
Ye, Pengqing
Zhen, Qianqian
Yao, Xinrong
Xu, Tong
Shao, Yinlin
Chen, Jiuxi
author_facet Hu, Kun
Ye, Pengqing
Zhen, Qianqian
Yao, Xinrong
Xu, Tong
Shao, Yinlin
Chen, Jiuxi
author_sort Hu, Kun
collection PubMed
description Palladium-catalyzed base-free addition of aryltriolborates to aldehydes has been developed, leading to a wide range of carbinol derivatives in good to excellent yields. The efficiency of this transformation was demonstrated by compatibility with a wide range of functional groups. The present synthetic route to carbinol derivatives could be readily scaled up to gram quantity without difficulty. Thus, this method represents a simple and practical procedure to access carbinol derivatives.
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spelling pubmed-61517802018-11-13 Efficient Approach to Carbinol Derivatives through Palladium-Catalyzed Base-Free Addition of Aryltriolborates to Aldehydes Hu, Kun Ye, Pengqing Zhen, Qianqian Yao, Xinrong Xu, Tong Shao, Yinlin Chen, Jiuxi Molecules Article Palladium-catalyzed base-free addition of aryltriolborates to aldehydes has been developed, leading to a wide range of carbinol derivatives in good to excellent yields. The efficiency of this transformation was demonstrated by compatibility with a wide range of functional groups. The present synthetic route to carbinol derivatives could be readily scaled up to gram quantity without difficulty. Thus, this method represents a simple and practical procedure to access carbinol derivatives. MDPI 2017-09-20 /pmc/articles/PMC6151780/ /pubmed/28930180 http://dx.doi.org/10.3390/molecules22091580 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hu, Kun
Ye, Pengqing
Zhen, Qianqian
Yao, Xinrong
Xu, Tong
Shao, Yinlin
Chen, Jiuxi
Efficient Approach to Carbinol Derivatives through Palladium-Catalyzed Base-Free Addition of Aryltriolborates to Aldehydes
title Efficient Approach to Carbinol Derivatives through Palladium-Catalyzed Base-Free Addition of Aryltriolborates to Aldehydes
title_full Efficient Approach to Carbinol Derivatives through Palladium-Catalyzed Base-Free Addition of Aryltriolborates to Aldehydes
title_fullStr Efficient Approach to Carbinol Derivatives through Palladium-Catalyzed Base-Free Addition of Aryltriolborates to Aldehydes
title_full_unstemmed Efficient Approach to Carbinol Derivatives through Palladium-Catalyzed Base-Free Addition of Aryltriolborates to Aldehydes
title_short Efficient Approach to Carbinol Derivatives through Palladium-Catalyzed Base-Free Addition of Aryltriolborates to Aldehydes
title_sort efficient approach to carbinol derivatives through palladium-catalyzed base-free addition of aryltriolborates to aldehydes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151780/
https://www.ncbi.nlm.nih.gov/pubmed/28930180
http://dx.doi.org/10.3390/molecules22091580
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