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First Organocatalytic Asymmetric Synthesis of 1-Benzamido-1,4-Dihydropyridine Derivatives

Preliminary results concerning the first asymmetric synthesis of highly functionalized 1-benzamido-1,4-dihydropyridine derivatives via the reaction of hydrazones with alkylidenemalononitriles in the presence of β-isocupreidine catalyst are reported. The moderate, but promising, enantioselectivity ob...

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Autores principales: Auria-Luna, Fernando, Marqués-López, Eugenia, P. Herrera, Raquel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222298/
https://www.ncbi.nlm.nih.gov/pubmed/30347659
http://dx.doi.org/10.3390/molecules23102692
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author Auria-Luna, Fernando
Marqués-López, Eugenia
P. Herrera, Raquel
author_facet Auria-Luna, Fernando
Marqués-López, Eugenia
P. Herrera, Raquel
author_sort Auria-Luna, Fernando
collection PubMed
description Preliminary results concerning the first asymmetric synthesis of highly functionalized 1-benzamido-1,4-dihydropyridine derivatives via the reaction of hydrazones with alkylidenemalononitriles in the presence of β-isocupreidine catalyst are reported. The moderate, but promising, enantioselectivity observed (40–54% ee), opens the door to a new area of research for the asymmetric construction of new chiral 1,4-dihydropyridine derivatives, whose enantioselective catalytic preparation are still very limited. Moreover, the use of hydrazones for the enantioselective construction of chiral 1,4-dihydropyridines has been overlooked in the literature so far. Therefore, our research represents a pivotal example in this field which remains still unexplored.
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spelling pubmed-62222982018-11-13 First Organocatalytic Asymmetric Synthesis of 1-Benzamido-1,4-Dihydropyridine Derivatives Auria-Luna, Fernando Marqués-López, Eugenia P. Herrera, Raquel Molecules Communication Preliminary results concerning the first asymmetric synthesis of highly functionalized 1-benzamido-1,4-dihydropyridine derivatives via the reaction of hydrazones with alkylidenemalononitriles in the presence of β-isocupreidine catalyst are reported. The moderate, but promising, enantioselectivity observed (40–54% ee), opens the door to a new area of research for the asymmetric construction of new chiral 1,4-dihydropyridine derivatives, whose enantioselective catalytic preparation are still very limited. Moreover, the use of hydrazones for the enantioselective construction of chiral 1,4-dihydropyridines has been overlooked in the literature so far. Therefore, our research represents a pivotal example in this field which remains still unexplored. MDPI 2018-10-19 /pmc/articles/PMC6222298/ /pubmed/30347659 http://dx.doi.org/10.3390/molecules23102692 Text en © 2018 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 Communication
Auria-Luna, Fernando
Marqués-López, Eugenia
P. Herrera, Raquel
First Organocatalytic Asymmetric Synthesis of 1-Benzamido-1,4-Dihydropyridine Derivatives
title First Organocatalytic Asymmetric Synthesis of 1-Benzamido-1,4-Dihydropyridine Derivatives
title_full First Organocatalytic Asymmetric Synthesis of 1-Benzamido-1,4-Dihydropyridine Derivatives
title_fullStr First Organocatalytic Asymmetric Synthesis of 1-Benzamido-1,4-Dihydropyridine Derivatives
title_full_unstemmed First Organocatalytic Asymmetric Synthesis of 1-Benzamido-1,4-Dihydropyridine Derivatives
title_short First Organocatalytic Asymmetric Synthesis of 1-Benzamido-1,4-Dihydropyridine Derivatives
title_sort first organocatalytic asymmetric synthesis of 1-benzamido-1,4-dihydropyridine derivatives
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222298/
https://www.ncbi.nlm.nih.gov/pubmed/30347659
http://dx.doi.org/10.3390/molecules23102692
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