Amberlite-15 promoted an unprecedented aza Michael rearrangement for one pot synthesis of dihydroquinazolinone compounds

A new one pot multicomponent annulation strategy for the synthesis of various dihydroquinazolinone compounds has been developed using Amberlite-15 as a catalyst, giving good to moderate yields. In this reaction the substrate scope for amines and aldehydes was also investigated. The reaction has been...

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Detalles Bibliográficos
Autores principales: Murthy, V. Narayana, Nikumbh, Satish P., Tadiparthi, Krishnaji, Madhubabu, M. V., Jammula, Subba Rao, Rao, L. Vaikunta, Raghunadh, Akula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092434/
https://www.ncbi.nlm.nih.gov/pubmed/35558548
http://dx.doi.org/10.1039/c8ra03308k
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author Murthy, V. Narayana
Nikumbh, Satish P.
Tadiparthi, Krishnaji
Madhubabu, M. V.
Jammula, Subba Rao
Rao, L. Vaikunta
Raghunadh, Akula
author_facet Murthy, V. Narayana
Nikumbh, Satish P.
Tadiparthi, Krishnaji
Madhubabu, M. V.
Jammula, Subba Rao
Rao, L. Vaikunta
Raghunadh, Akula
author_sort Murthy, V. Narayana
collection PubMed
description A new one pot multicomponent annulation strategy for the synthesis of various dihydroquinazolinone compounds has been developed using Amberlite-15 as a catalyst, giving good to moderate yields. In this reaction the substrate scope for amines and aldehydes was also investigated. The reaction has been checked on a large scale and the possible reaction mechanism has also been proposed.
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spelling pubmed-90924342022-05-11 Amberlite-15 promoted an unprecedented aza Michael rearrangement for one pot synthesis of dihydroquinazolinone compounds Murthy, V. Narayana Nikumbh, Satish P. Tadiparthi, Krishnaji Madhubabu, M. V. Jammula, Subba Rao Rao, L. Vaikunta Raghunadh, Akula RSC Adv Chemistry A new one pot multicomponent annulation strategy for the synthesis of various dihydroquinazolinone compounds has been developed using Amberlite-15 as a catalyst, giving good to moderate yields. In this reaction the substrate scope for amines and aldehydes was also investigated. The reaction has been checked on a large scale and the possible reaction mechanism has also been proposed. The Royal Society of Chemistry 2018-06-19 /pmc/articles/PMC9092434/ /pubmed/35558548 http://dx.doi.org/10.1039/c8ra03308k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Murthy, V. Narayana
Nikumbh, Satish P.
Tadiparthi, Krishnaji
Madhubabu, M. V.
Jammula, Subba Rao
Rao, L. Vaikunta
Raghunadh, Akula
Amberlite-15 promoted an unprecedented aza Michael rearrangement for one pot synthesis of dihydroquinazolinone compounds
title Amberlite-15 promoted an unprecedented aza Michael rearrangement for one pot synthesis of dihydroquinazolinone compounds
title_full Amberlite-15 promoted an unprecedented aza Michael rearrangement for one pot synthesis of dihydroquinazolinone compounds
title_fullStr Amberlite-15 promoted an unprecedented aza Michael rearrangement for one pot synthesis of dihydroquinazolinone compounds
title_full_unstemmed Amberlite-15 promoted an unprecedented aza Michael rearrangement for one pot synthesis of dihydroquinazolinone compounds
title_short Amberlite-15 promoted an unprecedented aza Michael rearrangement for one pot synthesis of dihydroquinazolinone compounds
title_sort amberlite-15 promoted an unprecedented aza michael rearrangement for one pot synthesis of dihydroquinazolinone compounds
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092434/
https://www.ncbi.nlm.nih.gov/pubmed/35558548
http://dx.doi.org/10.1039/c8ra03308k
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