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A Facile Synthesis of 3-Substituted 9H-Pyrido[3,4-b]indol-1(2H)-one Derivatives from 3-Substituted β-Carbolines
A mild and efficient two-step synthesis of 3-substituted β-carbolinone derivatives from 3-substituted β-carboline in good yields is described. A possible reaction mechanism for the formation of the skeleton of β-carbolin-1-one is proposed. The structures of these compounds were established by IR, (1...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257788/ https://www.ncbi.nlm.nih.gov/pubmed/20717074 http://dx.doi.org/10.3390/molecules15085680 |
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author | Lin, Guowu Wang, Yue Zhou, Qingfa Tang, Weifang Wang, Jian Lu, Tao |
author_facet | Lin, Guowu Wang, Yue Zhou, Qingfa Tang, Weifang Wang, Jian Lu, Tao |
author_sort | Lin, Guowu |
collection | PubMed |
description | A mild and efficient two-step synthesis of 3-substituted β-carbolinone derivatives from 3-substituted β-carboline in good yields is described. A possible reaction mechanism for the formation of the skeleton of β-carbolin-1-one is proposed. The structures of these compounds were established by IR, (1)H-NMR, (1)(3)C-NMR, mass spectrometry and elemental analysis, as well as X-ray crystallographic analysis of 4-2 and 6-2. |
format | Online Article Text |
id | pubmed-6257788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62577882018-12-06 A Facile Synthesis of 3-Substituted 9H-Pyrido[3,4-b]indol-1(2H)-one Derivatives from 3-Substituted β-Carbolines Lin, Guowu Wang, Yue Zhou, Qingfa Tang, Weifang Wang, Jian Lu, Tao Molecules Article A mild and efficient two-step synthesis of 3-substituted β-carbolinone derivatives from 3-substituted β-carboline in good yields is described. A possible reaction mechanism for the formation of the skeleton of β-carbolin-1-one is proposed. The structures of these compounds were established by IR, (1)H-NMR, (1)(3)C-NMR, mass spectrometry and elemental analysis, as well as X-ray crystallographic analysis of 4-2 and 6-2. MDPI 2010-08-17 /pmc/articles/PMC6257788/ /pubmed/20717074 http://dx.doi.org/10.3390/molecules15085680 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ 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 Lin, Guowu Wang, Yue Zhou, Qingfa Tang, Weifang Wang, Jian Lu, Tao A Facile Synthesis of 3-Substituted 9H-Pyrido[3,4-b]indol-1(2H)-one Derivatives from 3-Substituted β-Carbolines |
title | A Facile Synthesis of 3-Substituted 9H-Pyrido[3,4-b]indol-1(2H)-one Derivatives from 3-Substituted β-Carbolines |
title_full | A Facile Synthesis of 3-Substituted 9H-Pyrido[3,4-b]indol-1(2H)-one Derivatives from 3-Substituted β-Carbolines |
title_fullStr | A Facile Synthesis of 3-Substituted 9H-Pyrido[3,4-b]indol-1(2H)-one Derivatives from 3-Substituted β-Carbolines |
title_full_unstemmed | A Facile Synthesis of 3-Substituted 9H-Pyrido[3,4-b]indol-1(2H)-one Derivatives from 3-Substituted β-Carbolines |
title_short | A Facile Synthesis of 3-Substituted 9H-Pyrido[3,4-b]indol-1(2H)-one Derivatives from 3-Substituted β-Carbolines |
title_sort | facile synthesis of 3-substituted 9h-pyrido[3,4-b]indol-1(2h)-one derivatives from 3-substituted β-carbolines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257788/ https://www.ncbi.nlm.nih.gov/pubmed/20717074 http://dx.doi.org/10.3390/molecules15085680 |
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