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Cs(2)CO(3)-Initiated Trifluoro-Methylation of Chalcones and Ketones for Practical Synthesis of Trifluoromethylated Tertiary Silyl Ethers
It was found that 1,2-trifluoromethylation reactions of ketones, enones, and aldehydes were easily accomplished using the Prakash reagent in the presence of catalytic amounts of cesium carbonate, which represents an experimentally convenient, atom-economic process for this anionic trifluoromethylati...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154635/ https://www.ncbi.nlm.nih.gov/pubmed/28524100 http://dx.doi.org/10.3390/molecules22050769 |
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author | Dong, Cheng Bai, Xing-Feng Lv, Ji-Yuan Cui, Yu-Ming Cao, Jian Zheng, Zhan-Jiang Xu, Li-Wen |
author_facet | Dong, Cheng Bai, Xing-Feng Lv, Ji-Yuan Cui, Yu-Ming Cao, Jian Zheng, Zhan-Jiang Xu, Li-Wen |
author_sort | Dong, Cheng |
collection | PubMed |
description | It was found that 1,2-trifluoromethylation reactions of ketones, enones, and aldehydes were easily accomplished using the Prakash reagent in the presence of catalytic amounts of cesium carbonate, which represents an experimentally convenient, atom-economic process for this anionic trifluoromethylation of non-enolisable aldehydes and ketones. |
format | Online Article Text |
id | pubmed-6154635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61546352018-11-13 Cs(2)CO(3)-Initiated Trifluoro-Methylation of Chalcones and Ketones for Practical Synthesis of Trifluoromethylated Tertiary Silyl Ethers Dong, Cheng Bai, Xing-Feng Lv, Ji-Yuan Cui, Yu-Ming Cao, Jian Zheng, Zhan-Jiang Xu, Li-Wen Molecules Article It was found that 1,2-trifluoromethylation reactions of ketones, enones, and aldehydes were easily accomplished using the Prakash reagent in the presence of catalytic amounts of cesium carbonate, which represents an experimentally convenient, atom-economic process for this anionic trifluoromethylation of non-enolisable aldehydes and ketones. MDPI 2017-05-18 /pmc/articles/PMC6154635/ /pubmed/28524100 http://dx.doi.org/10.3390/molecules22050769 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 Dong, Cheng Bai, Xing-Feng Lv, Ji-Yuan Cui, Yu-Ming Cao, Jian Zheng, Zhan-Jiang Xu, Li-Wen Cs(2)CO(3)-Initiated Trifluoro-Methylation of Chalcones and Ketones for Practical Synthesis of Trifluoromethylated Tertiary Silyl Ethers |
title | Cs(2)CO(3)-Initiated Trifluoro-Methylation of Chalcones and Ketones for Practical Synthesis of Trifluoromethylated Tertiary Silyl Ethers |
title_full | Cs(2)CO(3)-Initiated Trifluoro-Methylation of Chalcones and Ketones for Practical Synthesis of Trifluoromethylated Tertiary Silyl Ethers |
title_fullStr | Cs(2)CO(3)-Initiated Trifluoro-Methylation of Chalcones and Ketones for Practical Synthesis of Trifluoromethylated Tertiary Silyl Ethers |
title_full_unstemmed | Cs(2)CO(3)-Initiated Trifluoro-Methylation of Chalcones and Ketones for Practical Synthesis of Trifluoromethylated Tertiary Silyl Ethers |
title_short | Cs(2)CO(3)-Initiated Trifluoro-Methylation of Chalcones and Ketones for Practical Synthesis of Trifluoromethylated Tertiary Silyl Ethers |
title_sort | cs(2)co(3)-initiated trifluoro-methylation of chalcones and ketones for practical synthesis of trifluoromethylated tertiary silyl ethers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154635/ https://www.ncbi.nlm.nih.gov/pubmed/28524100 http://dx.doi.org/10.3390/molecules22050769 |
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