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Ruthenium-catalyzed decarboxylative C–S cross-coupling of carbonothioate: synthesis of allyl(aryl)sulfide
A novel ruthenium-catalyzed decarboxylative cross-coupling of carbonothioate is disclosed. This method provides straightforward access to the corresponding allyl(aryl)sulfide derivatives in generally good to excellent yields under mild conditions and features a broad substrate scope, wide group tole...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082320/ https://www.ncbi.nlm.nih.gov/pubmed/35542144 http://dx.doi.org/10.1039/c8ra04783a |
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author | Zheng, Ren-Hua Guo, Hai-Chang Chen, Ting-Ting Huang, Qing Huang, Guo-Bo Jiang, Hua-Jiang |
author_facet | Zheng, Ren-Hua Guo, Hai-Chang Chen, Ting-Ting Huang, Qing Huang, Guo-Bo Jiang, Hua-Jiang |
author_sort | Zheng, Ren-Hua |
collection | PubMed |
description | A novel ruthenium-catalyzed decarboxylative cross-coupling of carbonothioate is disclosed. This method provides straightforward access to the corresponding allyl(aryl)sulfide derivatives in generally good to excellent yields under mild conditions and features a broad substrate scope, wide group tolerance and in particular, no need to use halocarbon precursors. |
format | Online Article Text |
id | pubmed-9082320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90823202022-05-09 Ruthenium-catalyzed decarboxylative C–S cross-coupling of carbonothioate: synthesis of allyl(aryl)sulfide Zheng, Ren-Hua Guo, Hai-Chang Chen, Ting-Ting Huang, Qing Huang, Guo-Bo Jiang, Hua-Jiang RSC Adv Chemistry A novel ruthenium-catalyzed decarboxylative cross-coupling of carbonothioate is disclosed. This method provides straightforward access to the corresponding allyl(aryl)sulfide derivatives in generally good to excellent yields under mild conditions and features a broad substrate scope, wide group tolerance and in particular, no need to use halocarbon precursors. The Royal Society of Chemistry 2018-07-12 /pmc/articles/PMC9082320/ /pubmed/35542144 http://dx.doi.org/10.1039/c8ra04783a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Zheng, Ren-Hua Guo, Hai-Chang Chen, Ting-Ting Huang, Qing Huang, Guo-Bo Jiang, Hua-Jiang Ruthenium-catalyzed decarboxylative C–S cross-coupling of carbonothioate: synthesis of allyl(aryl)sulfide |
title | Ruthenium-catalyzed decarboxylative C–S cross-coupling of carbonothioate: synthesis of allyl(aryl)sulfide |
title_full | Ruthenium-catalyzed decarboxylative C–S cross-coupling of carbonothioate: synthesis of allyl(aryl)sulfide |
title_fullStr | Ruthenium-catalyzed decarboxylative C–S cross-coupling of carbonothioate: synthesis of allyl(aryl)sulfide |
title_full_unstemmed | Ruthenium-catalyzed decarboxylative C–S cross-coupling of carbonothioate: synthesis of allyl(aryl)sulfide |
title_short | Ruthenium-catalyzed decarboxylative C–S cross-coupling of carbonothioate: synthesis of allyl(aryl)sulfide |
title_sort | ruthenium-catalyzed decarboxylative c–s cross-coupling of carbonothioate: synthesis of allyl(aryl)sulfide |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082320/ https://www.ncbi.nlm.nih.gov/pubmed/35542144 http://dx.doi.org/10.1039/c8ra04783a |
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