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Formal aromaticity transfer for palladium-catalyzed coupling between phenols and pyrrolidines/indolines
We herein describe a palladium-catalyzed formal aromaticity transfer coupling reaction between phenols and pyrrolidines or indolines to generate the corresponding N-cyclohexyl pyrroles or indoles. In this transformation, the aromaticity of phenols is formally passed on to the pyrrolidine or indoline...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642148/ https://www.ncbi.nlm.nih.gov/pubmed/29147521 http://dx.doi.org/10.1039/c7sc02578e |
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author | Qiu, Zihang Li, Jiang-Sheng Li, Chao-Jun |
author_facet | Qiu, Zihang Li, Jiang-Sheng Li, Chao-Jun |
author_sort | Qiu, Zihang |
collection | PubMed |
description | We herein describe a palladium-catalyzed formal aromaticity transfer coupling reaction between phenols and pyrrolidines or indolines to generate the corresponding N-cyclohexyl pyrroles or indoles. In this transformation, the aromaticity of phenols is formally passed on to the pyrrolidine or indoline units. Substituted phenols thus can serve as latent cyclohexyl equivalents for the fast construction of various N-cyclohexyl pyrroles and indoles. |
format | Online Article Text |
id | pubmed-5642148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-56421482017-11-16 Formal aromaticity transfer for palladium-catalyzed coupling between phenols and pyrrolidines/indolines Qiu, Zihang Li, Jiang-Sheng Li, Chao-Jun Chem Sci Chemistry We herein describe a palladium-catalyzed formal aromaticity transfer coupling reaction between phenols and pyrrolidines or indolines to generate the corresponding N-cyclohexyl pyrroles or indoles. In this transformation, the aromaticity of phenols is formally passed on to the pyrrolidine or indoline units. Substituted phenols thus can serve as latent cyclohexyl equivalents for the fast construction of various N-cyclohexyl pyrroles and indoles. Royal Society of Chemistry 2017-10-01 2017-08-10 /pmc/articles/PMC5642148/ /pubmed/29147521 http://dx.doi.org/10.1039/c7sc02578e Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Qiu, Zihang Li, Jiang-Sheng Li, Chao-Jun Formal aromaticity transfer for palladium-catalyzed coupling between phenols and pyrrolidines/indolines |
title | Formal aromaticity transfer for palladium-catalyzed coupling between phenols and pyrrolidines/indolines
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title_full | Formal aromaticity transfer for palladium-catalyzed coupling between phenols and pyrrolidines/indolines
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title_fullStr | Formal aromaticity transfer for palladium-catalyzed coupling between phenols and pyrrolidines/indolines
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title_full_unstemmed | Formal aromaticity transfer for palladium-catalyzed coupling between phenols and pyrrolidines/indolines
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title_short | Formal aromaticity transfer for palladium-catalyzed coupling between phenols and pyrrolidines/indolines
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title_sort | formal aromaticity transfer for palladium-catalyzed coupling between phenols and pyrrolidines/indolines |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642148/ https://www.ncbi.nlm.nih.gov/pubmed/29147521 http://dx.doi.org/10.1039/c7sc02578e |
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