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Synthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanes

Imidazo[1,5-a]pyridines were efficiently prepared via the cyclization of 2-picolylamines with nitroalkanes electrophilically activated in the presence of phosphorous acid in polyphosphoric acid (PPA) medium.

Detalles Bibliográficos
Autores principales: Aksenov, Dmitrii A, Arutiunov, Nikolai A, Maliuga, Vladimir V, Aksenov, Alexander V, Rubin, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705866/
https://www.ncbi.nlm.nih.gov/pubmed/33299488
http://dx.doi.org/10.3762/bjoc.16.239
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author Aksenov, Dmitrii A
Arutiunov, Nikolai A
Maliuga, Vladimir V
Aksenov, Alexander V
Rubin, Michael
author_facet Aksenov, Dmitrii A
Arutiunov, Nikolai A
Maliuga, Vladimir V
Aksenov, Alexander V
Rubin, Michael
author_sort Aksenov, Dmitrii A
collection PubMed
description Imidazo[1,5-a]pyridines were efficiently prepared via the cyclization of 2-picolylamines with nitroalkanes electrophilically activated in the presence of phosphorous acid in polyphosphoric acid (PPA) medium.
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spelling pubmed-77058662020-12-08 Synthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanes Aksenov, Dmitrii A Arutiunov, Nikolai A Maliuga, Vladimir V Aksenov, Alexander V Rubin, Michael Beilstein J Org Chem Full Research Paper Imidazo[1,5-a]pyridines were efficiently prepared via the cyclization of 2-picolylamines with nitroalkanes electrophilically activated in the presence of phosphorous acid in polyphosphoric acid (PPA) medium. Beilstein-Institut 2020-11-26 /pmc/articles/PMC7705866/ /pubmed/33299488 http://dx.doi.org/10.3762/bjoc.16.239 Text en Copyright © 2020, Aksenov et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Aksenov, Dmitrii A
Arutiunov, Nikolai A
Maliuga, Vladimir V
Aksenov, Alexander V
Rubin, Michael
Synthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanes
title Synthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanes
title_full Synthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanes
title_fullStr Synthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanes
title_full_unstemmed Synthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanes
title_short Synthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanes
title_sort synthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanes
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705866/
https://www.ncbi.nlm.nih.gov/pubmed/33299488
http://dx.doi.org/10.3762/bjoc.16.239
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