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Copper-catalyzed reaction of aziridine for the synthesis of substituted imidazolidine and imidazolidinone

Herein we report a copper-catalyzed synthesis of imidazolidine by employing the reaction of aziridine with imine. The reaction smoothly provided a diverse range of 2-substituted imidazolidines with high compatibility with various functional groups. Moreover, during our investigation, we discovered t...

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Detalles Bibliográficos
Autores principales: Hashimoto, Kota, Higuchi, Daiki, Matsubara, Satoshi, Murakami, Kei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570437/
https://www.ncbi.nlm.nih.gov/pubmed/37841205
http://dx.doi.org/10.3389/fchem.2023.1272034
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author Hashimoto, Kota
Higuchi, Daiki
Matsubara, Satoshi
Murakami, Kei
author_facet Hashimoto, Kota
Higuchi, Daiki
Matsubara, Satoshi
Murakami, Kei
author_sort Hashimoto, Kota
collection PubMed
description Herein we report a copper-catalyzed synthesis of imidazolidine by employing the reaction of aziridine with imine. The reaction smoothly provided a diverse range of 2-substituted imidazolidines with high compatibility with various functional groups. Moreover, during our investigation, we discovered that isocyanate also reacted with aziridine to yield substituted imidazolidinones efficiently. The versatility of these reactions was further demonstrated by their application in the synthesis of hybrid molecules derived from two pharmaceutical compounds. This approach opens new possibilities for the discovery of novel classes of bioactive molecules.
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spelling pubmed-105704372023-10-14 Copper-catalyzed reaction of aziridine for the synthesis of substituted imidazolidine and imidazolidinone Hashimoto, Kota Higuchi, Daiki Matsubara, Satoshi Murakami, Kei Front Chem Chemistry Herein we report a copper-catalyzed synthesis of imidazolidine by employing the reaction of aziridine with imine. The reaction smoothly provided a diverse range of 2-substituted imidazolidines with high compatibility with various functional groups. Moreover, during our investigation, we discovered that isocyanate also reacted with aziridine to yield substituted imidazolidinones efficiently. The versatility of these reactions was further demonstrated by their application in the synthesis of hybrid molecules derived from two pharmaceutical compounds. This approach opens new possibilities for the discovery of novel classes of bioactive molecules. Frontiers Media S.A. 2023-09-29 /pmc/articles/PMC10570437/ /pubmed/37841205 http://dx.doi.org/10.3389/fchem.2023.1272034 Text en Copyright © 2023 Hashimoto, Higuchi, Matsubara and Murakami. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Hashimoto, Kota
Higuchi, Daiki
Matsubara, Satoshi
Murakami, Kei
Copper-catalyzed reaction of aziridine for the synthesis of substituted imidazolidine and imidazolidinone
title Copper-catalyzed reaction of aziridine for the synthesis of substituted imidazolidine and imidazolidinone
title_full Copper-catalyzed reaction of aziridine for the synthesis of substituted imidazolidine and imidazolidinone
title_fullStr Copper-catalyzed reaction of aziridine for the synthesis of substituted imidazolidine and imidazolidinone
title_full_unstemmed Copper-catalyzed reaction of aziridine for the synthesis of substituted imidazolidine and imidazolidinone
title_short Copper-catalyzed reaction of aziridine for the synthesis of substituted imidazolidine and imidazolidinone
title_sort copper-catalyzed reaction of aziridine for the synthesis of substituted imidazolidine and imidazolidinone
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570437/
https://www.ncbi.nlm.nih.gov/pubmed/37841205
http://dx.doi.org/10.3389/fchem.2023.1272034
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