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Synthesis of Novel N-Heterocyclic Compounds Containing 1,2,3-Triazole Ring System via Domino, “Click” and RDA Reactions

An uncomplicated, high-yielding synthetic route has been developed to constitute complicated heterocycles, applying domino, click and retro-Diels–Alder (RDA) reaction sequences. Starting from 2-aminocarboxamides, a new set of isoindolo[2,1-a]quinazolinones was synthesized with domino ring closure. A...

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Detalles Bibliográficos
Autores principales: Palkó, Márta, El Haimer, Mohamed, Kormányos, Zsanett, Fülöp, Ferenc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412576/
https://www.ncbi.nlm.nih.gov/pubmed/30795610
http://dx.doi.org/10.3390/molecules24040772
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author Palkó, Márta
El Haimer, Mohamed
Kormányos, Zsanett
Fülöp, Ferenc
author_facet Palkó, Márta
El Haimer, Mohamed
Kormányos, Zsanett
Fülöp, Ferenc
author_sort Palkó, Márta
collection PubMed
description An uncomplicated, high-yielding synthetic route has been developed to constitute complicated heterocycles, applying domino, click and retro-Diels–Alder (RDA) reaction sequences. Starting from 2-aminocarboxamides, a new set of isoindolo[2,1-a]quinazolinones was synthesized with domino ring closure. A click reaction was performed to create the 1,2,3-triazole heterocyclic ring, followed by an RDA reaction resulting in dihydropyrimido[2,1-a]isoindole-2,6-diones. The absolute configuration, concluded by the norbornene structure that served as a chiral source, remained constant throughout the transformations. The structure of the synthesized compounds was examined by (1)H and (13)C Nuclear Magnetic Resonance (NMR) methods.
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spelling pubmed-64125762019-04-09 Synthesis of Novel N-Heterocyclic Compounds Containing 1,2,3-Triazole Ring System via Domino, “Click” and RDA Reactions Palkó, Márta El Haimer, Mohamed Kormányos, Zsanett Fülöp, Ferenc Molecules Article An uncomplicated, high-yielding synthetic route has been developed to constitute complicated heterocycles, applying domino, click and retro-Diels–Alder (RDA) reaction sequences. Starting from 2-aminocarboxamides, a new set of isoindolo[2,1-a]quinazolinones was synthesized with domino ring closure. A click reaction was performed to create the 1,2,3-triazole heterocyclic ring, followed by an RDA reaction resulting in dihydropyrimido[2,1-a]isoindole-2,6-diones. The absolute configuration, concluded by the norbornene structure that served as a chiral source, remained constant throughout the transformations. The structure of the synthesized compounds was examined by (1)H and (13)C Nuclear Magnetic Resonance (NMR) methods. MDPI 2019-02-21 /pmc/articles/PMC6412576/ /pubmed/30795610 http://dx.doi.org/10.3390/molecules24040772 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 Article
Palkó, Márta
El Haimer, Mohamed
Kormányos, Zsanett
Fülöp, Ferenc
Synthesis of Novel N-Heterocyclic Compounds Containing 1,2,3-Triazole Ring System via Domino, “Click” and RDA Reactions
title Synthesis of Novel N-Heterocyclic Compounds Containing 1,2,3-Triazole Ring System via Domino, “Click” and RDA Reactions
title_full Synthesis of Novel N-Heterocyclic Compounds Containing 1,2,3-Triazole Ring System via Domino, “Click” and RDA Reactions
title_fullStr Synthesis of Novel N-Heterocyclic Compounds Containing 1,2,3-Triazole Ring System via Domino, “Click” and RDA Reactions
title_full_unstemmed Synthesis of Novel N-Heterocyclic Compounds Containing 1,2,3-Triazole Ring System via Domino, “Click” and RDA Reactions
title_short Synthesis of Novel N-Heterocyclic Compounds Containing 1,2,3-Triazole Ring System via Domino, “Click” and RDA Reactions
title_sort synthesis of novel n-heterocyclic compounds containing 1,2,3-triazole ring system via domino, “click” and rda reactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412576/
https://www.ncbi.nlm.nih.gov/pubmed/30795610
http://dx.doi.org/10.3390/molecules24040772
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