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RuCl(3)·3H(2)O Catalyzed Reactions: Facile Synthesis of Bis(indolyl)methanes under Mild Conditions
RuCl(3)·3H(2)O was found to be an effective catalyst for reactions of indoles, 2-methylthiophene, and 2-methylfuran with aldehydes to afford the corresponding bis(indolyl)methanes, bis(thienyl)methanes, and bis(fur-2-yl)methanes in moderate to excellent yields. Experimental results indicated that mo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263275/ https://www.ncbi.nlm.nih.gov/pubmed/21555975 http://dx.doi.org/10.3390/molecules16053855 |
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author | Qu, Hong-En Xiao, Chen Wang, Ning Yu, Kai-Hui Hu, Qiao-Sheng Liu, Liang-Xian |
author_facet | Qu, Hong-En Xiao, Chen Wang, Ning Yu, Kai-Hui Hu, Qiao-Sheng Liu, Liang-Xian |
author_sort | Qu, Hong-En |
collection | PubMed |
description | RuCl(3)·3H(2)O was found to be an effective catalyst for reactions of indoles, 2-methylthiophene, and 2-methylfuran with aldehydes to afford the corresponding bis(indolyl)methanes, bis(thienyl)methanes, and bis(fur-2-yl)methanes in moderate to excellent yields. Experimental results indicated that mono(indolyl)methanol is not the reaction intermediate under these reaction conditions. |
format | Online Article Text |
id | pubmed-6263275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62632752018-12-10 RuCl(3)·3H(2)O Catalyzed Reactions: Facile Synthesis of Bis(indolyl)methanes under Mild Conditions Qu, Hong-En Xiao, Chen Wang, Ning Yu, Kai-Hui Hu, Qiao-Sheng Liu, Liang-Xian Molecules Article RuCl(3)·3H(2)O was found to be an effective catalyst for reactions of indoles, 2-methylthiophene, and 2-methylfuran with aldehydes to afford the corresponding bis(indolyl)methanes, bis(thienyl)methanes, and bis(fur-2-yl)methanes in moderate to excellent yields. Experimental results indicated that mono(indolyl)methanol is not the reaction intermediate under these reaction conditions. MDPI 2011-05-09 /pmc/articles/PMC6263275/ /pubmed/21555975 http://dx.doi.org/10.3390/molecules16053855 Text en © 2011 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Qu, Hong-En Xiao, Chen Wang, Ning Yu, Kai-Hui Hu, Qiao-Sheng Liu, Liang-Xian RuCl(3)·3H(2)O Catalyzed Reactions: Facile Synthesis of Bis(indolyl)methanes under Mild Conditions |
title | RuCl(3)·3H(2)O Catalyzed Reactions: Facile Synthesis of Bis(indolyl)methanes under Mild Conditions |
title_full | RuCl(3)·3H(2)O Catalyzed Reactions: Facile Synthesis of Bis(indolyl)methanes under Mild Conditions |
title_fullStr | RuCl(3)·3H(2)O Catalyzed Reactions: Facile Synthesis of Bis(indolyl)methanes under Mild Conditions |
title_full_unstemmed | RuCl(3)·3H(2)O Catalyzed Reactions: Facile Synthesis of Bis(indolyl)methanes under Mild Conditions |
title_short | RuCl(3)·3H(2)O Catalyzed Reactions: Facile Synthesis of Bis(indolyl)methanes under Mild Conditions |
title_sort | rucl(3)·3h(2)o catalyzed reactions: facile synthesis of bis(indolyl)methanes under mild conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263275/ https://www.ncbi.nlm.nih.gov/pubmed/21555975 http://dx.doi.org/10.3390/molecules16053855 |
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