Cargando…
Synthesis of N-substituted Acridinediones and Polyhydroquinoline Derivatives in Refluxing Water
Acridinediones were synthesized by the one-pot Hantzsch condensation of an aromatic aldehyde, 5,5-dimethyl-1,3-cyclohexanedione, and aniline/4-methylaniline in refluxing water. This method has then been extended to the four-component reaction of an aromatic aldehyde, 5,5-dimethyl-1,3-cyclohexanedion...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268734/ https://www.ncbi.nlm.nih.gov/pubmed/22565483 http://dx.doi.org/10.3390/molecules17055339 |
_version_ | 1783376354551529472 |
---|---|
author | Xia, Jing-Jing Zhang, Ke-Hua |
author_facet | Xia, Jing-Jing Zhang, Ke-Hua |
author_sort | Xia, Jing-Jing |
collection | PubMed |
description | Acridinediones were synthesized by the one-pot Hantzsch condensation of an aromatic aldehyde, 5,5-dimethyl-1,3-cyclohexanedione, and aniline/4-methylaniline in refluxing water. This method has then been extended to the four-component reaction of an aromatic aldehyde, 5,5-dimethyl-1,3-cyclohexanedione, ethyl acetoacetate and ammonium acetate for the synthesis of polyhydroquinoline derivatives. This is an environmentally friendly and efficient procedure providing good to excellent yields. |
format | Online Article Text |
id | pubmed-6268734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62687342018-12-20 Synthesis of N-substituted Acridinediones and Polyhydroquinoline Derivatives in Refluxing Water Xia, Jing-Jing Zhang, Ke-Hua Molecules Communication Acridinediones were synthesized by the one-pot Hantzsch condensation of an aromatic aldehyde, 5,5-dimethyl-1,3-cyclohexanedione, and aniline/4-methylaniline in refluxing water. This method has then been extended to the four-component reaction of an aromatic aldehyde, 5,5-dimethyl-1,3-cyclohexanedione, ethyl acetoacetate and ammonium acetate for the synthesis of polyhydroquinoline derivatives. This is an environmentally friendly and efficient procedure providing good to excellent yields. MDPI 2012-05-07 /pmc/articles/PMC6268734/ /pubmed/22565483 http://dx.doi.org/10.3390/molecules17055339 Text en © 2012 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 | Communication Xia, Jing-Jing Zhang, Ke-Hua Synthesis of N-substituted Acridinediones and Polyhydroquinoline Derivatives in Refluxing Water |
title | Synthesis of N-substituted Acridinediones and Polyhydroquinoline Derivatives in Refluxing Water |
title_full | Synthesis of N-substituted Acridinediones and Polyhydroquinoline Derivatives in Refluxing Water |
title_fullStr | Synthesis of N-substituted Acridinediones and Polyhydroquinoline Derivatives in Refluxing Water |
title_full_unstemmed | Synthesis of N-substituted Acridinediones and Polyhydroquinoline Derivatives in Refluxing Water |
title_short | Synthesis of N-substituted Acridinediones and Polyhydroquinoline Derivatives in Refluxing Water |
title_sort | synthesis of n-substituted acridinediones and polyhydroquinoline derivatives in refluxing water |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268734/ https://www.ncbi.nlm.nih.gov/pubmed/22565483 http://dx.doi.org/10.3390/molecules17055339 |
work_keys_str_mv | AT xiajingjing synthesisofnsubstitutedacridinedionesandpolyhydroquinolinederivativesinrefluxingwater AT zhangkehua synthesisofnsubstitutedacridinedionesandpolyhydroquinolinederivativesinrefluxingwater |