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Synthesis Chalones and Their Isomerization into Flavanones and Azaflavanones

Flavanones [2-aryl-2,3-dihydrochromen-4(1H)ones] and 2-aryl-2,3-dihydroquinolin-4(1H)-ones are valuable precursors in the synthesis of important pharmacological scaffolds, so efficient methodologies towards their synthesis are important in the medicinal chemistry context. Their synthesis also involv...

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Autores principales: Rocha, Djenisa H. A., Vaz, Patrícia A. A. M., Pinto, Diana C. G. A., Silva, Artur M. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789463/
https://www.ncbi.nlm.nih.gov/pubmed/31443245
http://dx.doi.org/10.3390/mps2030070
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author Rocha, Djenisa H. A.
Vaz, Patrícia A. A. M.
Pinto, Diana C. G. A.
Silva, Artur M. S.
author_facet Rocha, Djenisa H. A.
Vaz, Patrícia A. A. M.
Pinto, Diana C. G. A.
Silva, Artur M. S.
author_sort Rocha, Djenisa H. A.
collection PubMed
description Flavanones [2-aryl-2,3-dihydrochromen-4(1H)ones] and 2-aryl-2,3-dihydroquinolin-4(1H)-ones are valuable precursors in the synthesis of important pharmacological scaffolds, so efficient methodologies towards their synthesis are important in the medicinal chemistry context. Their synthesis also involves theoretical concepts such as aldol condensation, isomerization, and catalysis that make it useful in an undergraduate organic chemistry laboratory. The use of both microwave irradiation as a source of energy to promote reactions and efficient catalysts are considered within green chemistry principles, mostly because the reaction yields are improved and reaction time decreased. In this paper, the efficiency of microwave irradiation use in the synthesis of chalcone derivatives and efficient catalyst systems to promote their isomerization into flavanones and 2-aryl-2,3-dihydroquinolin-4(1H)-ones is demonstrated.
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spelling pubmed-67894632019-10-16 Synthesis Chalones and Their Isomerization into Flavanones and Azaflavanones Rocha, Djenisa H. A. Vaz, Patrícia A. A. M. Pinto, Diana C. G. A. Silva, Artur M. S. Methods Protoc Protocol Flavanones [2-aryl-2,3-dihydrochromen-4(1H)ones] and 2-aryl-2,3-dihydroquinolin-4(1H)-ones are valuable precursors in the synthesis of important pharmacological scaffolds, so efficient methodologies towards their synthesis are important in the medicinal chemistry context. Their synthesis also involves theoretical concepts such as aldol condensation, isomerization, and catalysis that make it useful in an undergraduate organic chemistry laboratory. The use of both microwave irradiation as a source of energy to promote reactions and efficient catalysts are considered within green chemistry principles, mostly because the reaction yields are improved and reaction time decreased. In this paper, the efficiency of microwave irradiation use in the synthesis of chalcone derivatives and efficient catalyst systems to promote their isomerization into flavanones and 2-aryl-2,3-dihydroquinolin-4(1H)-ones is demonstrated. MDPI 2019-08-15 /pmc/articles/PMC6789463/ /pubmed/31443245 http://dx.doi.org/10.3390/mps2030070 Text en © 2019 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Rocha, Djenisa H. A.
Vaz, Patrícia A. A. M.
Pinto, Diana C. G. A.
Silva, Artur M. S.
Synthesis Chalones and Their Isomerization into Flavanones and Azaflavanones
title Synthesis Chalones and Their Isomerization into Flavanones and Azaflavanones
title_full Synthesis Chalones and Their Isomerization into Flavanones and Azaflavanones
title_fullStr Synthesis Chalones and Their Isomerization into Flavanones and Azaflavanones
title_full_unstemmed Synthesis Chalones and Their Isomerization into Flavanones and Azaflavanones
title_short Synthesis Chalones and Their Isomerization into Flavanones and Azaflavanones
title_sort synthesis chalones and their isomerization into flavanones and azaflavanones
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789463/
https://www.ncbi.nlm.nih.gov/pubmed/31443245
http://dx.doi.org/10.3390/mps2030070
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