Multicomponent synthesis of pyrimido[4,5-b] quinolines over a carbocationic catalytic system

Trityl chloride (TrCl) was efficiently used as a neutral catalyst for the multicomponent cyclization reaction of an aldehyde with dimedone and 6-amino-1,3-dimethyluracil for the preparation of pyrimido[4,5-b] quinolines in chloroform under reflux condition.

Detalles Bibliográficos
Autores principales: Moosavi-Zare, Ahmad Reza, Najafi, Raha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543543/
https://www.ncbi.nlm.nih.gov/pubmed/37779154
http://dx.doi.org/10.1038/s41598-023-43793-5
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author Moosavi-Zare, Ahmad Reza
Najafi, Raha
author_facet Moosavi-Zare, Ahmad Reza
Najafi, Raha
author_sort Moosavi-Zare, Ahmad Reza
collection PubMed
description Trityl chloride (TrCl) was efficiently used as a neutral catalyst for the multicomponent cyclization reaction of an aldehyde with dimedone and 6-amino-1,3-dimethyluracil for the preparation of pyrimido[4,5-b] quinolines in chloroform under reflux condition.
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spelling pubmed-105435432023-10-03 Multicomponent synthesis of pyrimido[4,5-b] quinolines over a carbocationic catalytic system Moosavi-Zare, Ahmad Reza Najafi, Raha Sci Rep Article Trityl chloride (TrCl) was efficiently used as a neutral catalyst for the multicomponent cyclization reaction of an aldehyde with dimedone and 6-amino-1,3-dimethyluracil for the preparation of pyrimido[4,5-b] quinolines in chloroform under reflux condition. Nature Publishing Group UK 2023-10-01 /pmc/articles/PMC10543543/ /pubmed/37779154 http://dx.doi.org/10.1038/s41598-023-43793-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Moosavi-Zare, Ahmad Reza
Najafi, Raha
Multicomponent synthesis of pyrimido[4,5-b] quinolines over a carbocationic catalytic system
title Multicomponent synthesis of pyrimido[4,5-b] quinolines over a carbocationic catalytic system
title_full Multicomponent synthesis of pyrimido[4,5-b] quinolines over a carbocationic catalytic system
title_fullStr Multicomponent synthesis of pyrimido[4,5-b] quinolines over a carbocationic catalytic system
title_full_unstemmed Multicomponent synthesis of pyrimido[4,5-b] quinolines over a carbocationic catalytic system
title_short Multicomponent synthesis of pyrimido[4,5-b] quinolines over a carbocationic catalytic system
title_sort multicomponent synthesis of pyrimido[4,5-b] quinolines over a carbocationic catalytic system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543543/
https://www.ncbi.nlm.nih.gov/pubmed/37779154
http://dx.doi.org/10.1038/s41598-023-43793-5
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