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Rhodium(iii) catalyzed olefination and deuteration of tetrahydrocarbazole
The rhodium-catalyzed olefination and deuteration of tetrahydrocarbazoles in water with the aid of an N,N-dimethylcarbamoyl-protected group is presented. This olefination method features a broad substrate scope, good functional-group tolerance, and high efficiency in water. Practical applications of...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698316/ https://www.ncbi.nlm.nih.gov/pubmed/35423333 http://dx.doi.org/10.1039/d1ra00236h |
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author | Peng, Wan Liu, Qiaohong Yin, Fucheng Shi, Cunjian Ji, Limei Qu, Lailiang Wang, Cheng Luo, Heng Kong, Lingyi Wang, Xiaobing |
author_facet | Peng, Wan Liu, Qiaohong Yin, Fucheng Shi, Cunjian Ji, Limei Qu, Lailiang Wang, Cheng Luo, Heng Kong, Lingyi Wang, Xiaobing |
author_sort | Peng, Wan |
collection | PubMed |
description | The rhodium-catalyzed olefination and deuteration of tetrahydrocarbazoles in water with the aid of an N,N-dimethylcarbamoyl-protected group is presented. This olefination method features a broad substrate scope, good functional-group tolerance, and high efficiency in water. Practical applications of the protocol are illustrated by the synthesis of various evodiamine derivatives. As such, this environmentally friendly approach to directly modify natural products will attract much attention in academic and industrial research. |
format | Online Article Text |
id | pubmed-8698316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86983162022-04-13 Rhodium(iii) catalyzed olefination and deuteration of tetrahydrocarbazole Peng, Wan Liu, Qiaohong Yin, Fucheng Shi, Cunjian Ji, Limei Qu, Lailiang Wang, Cheng Luo, Heng Kong, Lingyi Wang, Xiaobing RSC Adv Chemistry The rhodium-catalyzed olefination and deuteration of tetrahydrocarbazoles in water with the aid of an N,N-dimethylcarbamoyl-protected group is presented. This olefination method features a broad substrate scope, good functional-group tolerance, and high efficiency in water. Practical applications of the protocol are illustrated by the synthesis of various evodiamine derivatives. As such, this environmentally friendly approach to directly modify natural products will attract much attention in academic and industrial research. The Royal Society of Chemistry 2021-02-23 /pmc/articles/PMC8698316/ /pubmed/35423333 http://dx.doi.org/10.1039/d1ra00236h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Peng, Wan Liu, Qiaohong Yin, Fucheng Shi, Cunjian Ji, Limei Qu, Lailiang Wang, Cheng Luo, Heng Kong, Lingyi Wang, Xiaobing Rhodium(iii) catalyzed olefination and deuteration of tetrahydrocarbazole |
title | Rhodium(iii) catalyzed olefination and deuteration of tetrahydrocarbazole |
title_full | Rhodium(iii) catalyzed olefination and deuteration of tetrahydrocarbazole |
title_fullStr | Rhodium(iii) catalyzed olefination and deuteration of tetrahydrocarbazole |
title_full_unstemmed | Rhodium(iii) catalyzed olefination and deuteration of tetrahydrocarbazole |
title_short | Rhodium(iii) catalyzed olefination and deuteration of tetrahydrocarbazole |
title_sort | rhodium(iii) catalyzed olefination and deuteration of tetrahydrocarbazole |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698316/ https://www.ncbi.nlm.nih.gov/pubmed/35423333 http://dx.doi.org/10.1039/d1ra00236h |
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