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Efficient TCT-catalyzed Synthesis of 1,5-Benzodiazepine Derivatives under Mild Conditions
2,4,6-Trichloro-1,3,5-triazine (TCT) efficiently catalyzed the condensation reactions between 1,2-diamines and various enolizable ketones to afford 1,5-benzodiazepines in good to excellent yields. Simple and mild reaction conditions, the use of a cheap catalyst and easy workup and isolation are nota...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244957/ https://www.ncbi.nlm.nih.gov/pubmed/18830157 http://dx.doi.org/10.3390/molecules13092313 |
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author | Kuo, Chun-Wei Wang, Chun-Chao Kavala, Veerababurao Yao, Ching-Fa |
author_facet | Kuo, Chun-Wei Wang, Chun-Chao Kavala, Veerababurao Yao, Ching-Fa |
author_sort | Kuo, Chun-Wei |
collection | PubMed |
description | 2,4,6-Trichloro-1,3,5-triazine (TCT) efficiently catalyzed the condensation reactions between 1,2-diamines and various enolizable ketones to afford 1,5-benzodiazepines in good to excellent yields. Simple and mild reaction conditions, the use of a cheap catalyst and easy workup and isolation are notable features of this method. |
format | Online Article Text |
id | pubmed-6244957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62449572018-11-30 Efficient TCT-catalyzed Synthesis of 1,5-Benzodiazepine Derivatives under Mild Conditions Kuo, Chun-Wei Wang, Chun-Chao Kavala, Veerababurao Yao, Ching-Fa Molecules Article 2,4,6-Trichloro-1,3,5-triazine (TCT) efficiently catalyzed the condensation reactions between 1,2-diamines and various enolizable ketones to afford 1,5-benzodiazepines in good to excellent yields. Simple and mild reaction conditions, the use of a cheap catalyst and easy workup and isolation are notable features of this method. MDPI 2008-09-25 /pmc/articles/PMC6244957/ /pubmed/18830157 http://dx.doi.org/10.3390/molecules13092313 Text en © 2008 by the authors. Licensee Molecular Diversity Preservation International, 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 Kuo, Chun-Wei Wang, Chun-Chao Kavala, Veerababurao Yao, Ching-Fa Efficient TCT-catalyzed Synthesis of 1,5-Benzodiazepine Derivatives under Mild Conditions |
title | Efficient TCT-catalyzed Synthesis of 1,5-Benzodiazepine Derivatives under Mild Conditions |
title_full | Efficient TCT-catalyzed Synthesis of 1,5-Benzodiazepine Derivatives under Mild Conditions |
title_fullStr | Efficient TCT-catalyzed Synthesis of 1,5-Benzodiazepine Derivatives under Mild Conditions |
title_full_unstemmed | Efficient TCT-catalyzed Synthesis of 1,5-Benzodiazepine Derivatives under Mild Conditions |
title_short | Efficient TCT-catalyzed Synthesis of 1,5-Benzodiazepine Derivatives under Mild Conditions |
title_sort | efficient tct-catalyzed synthesis of 1,5-benzodiazepine derivatives under mild conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244957/ https://www.ncbi.nlm.nih.gov/pubmed/18830157 http://dx.doi.org/10.3390/molecules13092313 |
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