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Chlorotrifluoroethylidenes: an efficient and convenient approach to their synthesis
A convenient one step synthesis of chlorotrifluoroalkyl olefins starting from aldehydes was developed. The stable reagent 2-((1-chloro-2,2,2-trifluoroethyl)sulfonyl)benzothiazole was prepared from readily available benzothiazole-2-thiol and halothane. This method comprises using stable 2-((1-chloro-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053503/ https://www.ncbi.nlm.nih.gov/pubmed/35515602 http://dx.doi.org/10.1039/d0ra02481c |
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author | Upare, Abhay Atmaram Gadekar, Pradip K. Jadhav, Kiran Sivaramakrishnan, H. Roopan, Selvaraj Mohana |
author_facet | Upare, Abhay Atmaram Gadekar, Pradip K. Jadhav, Kiran Sivaramakrishnan, H. Roopan, Selvaraj Mohana |
author_sort | Upare, Abhay Atmaram |
collection | PubMed |
description | A convenient one step synthesis of chlorotrifluoroalkyl olefins starting from aldehydes was developed. The stable reagent 2-((1-chloro-2,2,2-trifluoroethyl)sulfonyl)benzothiazole was prepared from readily available benzothiazole-2-thiol and halothane. This method comprises using stable 2-((1-chloro-2,2,2-trifluoroethyl)sulfonyl)benzothiazole according to the Julia procedure and presents new opportunities for the synthesis of trifluoroalkylidene derivatives. |
format | Online Article Text |
id | pubmed-9053503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90535032022-05-04 Chlorotrifluoroethylidenes: an efficient and convenient approach to their synthesis Upare, Abhay Atmaram Gadekar, Pradip K. Jadhav, Kiran Sivaramakrishnan, H. Roopan, Selvaraj Mohana RSC Adv Chemistry A convenient one step synthesis of chlorotrifluoroalkyl olefins starting from aldehydes was developed. The stable reagent 2-((1-chloro-2,2,2-trifluoroethyl)sulfonyl)benzothiazole was prepared from readily available benzothiazole-2-thiol and halothane. This method comprises using stable 2-((1-chloro-2,2,2-trifluoroethyl)sulfonyl)benzothiazole according to the Julia procedure and presents new opportunities for the synthesis of trifluoroalkylidene derivatives. The Royal Society of Chemistry 2020-05-05 /pmc/articles/PMC9053503/ /pubmed/35515602 http://dx.doi.org/10.1039/d0ra02481c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Upare, Abhay Atmaram Gadekar, Pradip K. Jadhav, Kiran Sivaramakrishnan, H. Roopan, Selvaraj Mohana Chlorotrifluoroethylidenes: an efficient and convenient approach to their synthesis |
title | Chlorotrifluoroethylidenes: an efficient and convenient approach to their synthesis |
title_full | Chlorotrifluoroethylidenes: an efficient and convenient approach to their synthesis |
title_fullStr | Chlorotrifluoroethylidenes: an efficient and convenient approach to their synthesis |
title_full_unstemmed | Chlorotrifluoroethylidenes: an efficient and convenient approach to their synthesis |
title_short | Chlorotrifluoroethylidenes: an efficient and convenient approach to their synthesis |
title_sort | chlorotrifluoroethylidenes: an efficient and convenient approach to their synthesis |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053503/ https://www.ncbi.nlm.nih.gov/pubmed/35515602 http://dx.doi.org/10.1039/d0ra02481c |
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