Substrate‐Controlled Divergent Synthesis of Enaminones and Pyrroles from Indolizines and Nitroso Compounds
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Campo DC | Valor | Idioma |
---|---|---|
dc.contributor | Nuevos Materiales y Catalizadores (MATCAT) | es_ES |
dc.contributor.author | González Soria, María José | - |
dc.contributor.author | Alonso, Francisco | - |
dc.contributor.other | Universidad de Alicante. Departamento de Química Orgánica | es_ES |
dc.contributor.other | Universidad de Alicante. Instituto Universitario de Síntesis Orgánica | es_ES |
dc.date.accessioned | 2019-11-12T11:11:18Z | - |
dc.date.available | 2019-11-12T11:11:18Z | - |
dc.date.issued | 2019-11-05 | - |
dc.identifier.citation | Advanced Synthesis and Catalysis. 2019, 361(21): 5005-5017. doi:10.1002/adsc.201900837 | es_ES |
dc.identifier.issn | 1615-4150 (Print) | - |
dc.identifier.issn | 1615-4169 (Online) | - |
dc.identifier.uri | http://hdl.handle.net/10045/98751 | - |
dc.description.abstract | It is imperative to learn new synthetic transformations to succeed in drug discovery and development. We report the substrate‐driven synthesis of β‐enaminones and N‐aryl pyrroles from indolizines and nitrosoarenes; aryl‐substituted indolizines lead to β‐enaminones in a regio‐ and diastereoselective manner, whereas alkyl‐substituted indolizines produce tetrasubstituted pyrroles. All products contain a pyridine unit, the second most abundant ring (after phenyl) in the FDA Orange Book. In both cases, the reactions proceed at room temperature without any catalyst. Moreover, both types of products can be obtained in one pot from commercial materials as well as at a gram scale. It is worthy of note that the regioselectivity of the β‐enaminones is inaccessible by the standard literature methods and their utility has been exemplified in the synthesis of diverse heterocycles. We have made every endeavor to put forward the corresponding reaction mechanisms based on thorough experimental work. | es_ES |
dc.description.sponsorship | This work was generously supported by the Spanish Ministerio de Ciencia, Innovación y Universidades (MICIU; grant no. CTQ2017-88171-P), the Generalitat Valenciana (GV; grant no. AICO/2017/007), and the Instituto de Síntesis Orgánica (ISO). M.J.G.-S. is grateful to the ISO for a predoctoral grant (contract no. I-PAS-11/16). | es_ES |
dc.language | eng | es_ES |
dc.publisher | Wiley-VCH Verlag GmbH & Co. KGaA | es_ES |
dc.rights | © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim | es_ES |
dc.subject | Enaminones | es_ES |
dc.subject | Indolizines | es_ES |
dc.subject | Nitroso compounds | es_ES |
dc.subject | Nitrogen heterocycles | es_ES |
dc.subject | Pyrroles | es_ES |
dc.subject.other | Química Orgánica | es_ES |
dc.title | Substrate‐Controlled Divergent Synthesis of Enaminones and Pyrroles from Indolizines and Nitroso Compounds | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.peerreviewed | si | es_ES |
dc.identifier.doi | 10.1002/adsc.201900837 | - |
dc.relation.publisherversion | https://doi.org/10.1002/adsc.201900837 | es_ES |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2017-88171-P | - |
Aparece en las colecciones: | INV - MATCAT - Artículos de Revistas |
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Archivo | Descripción | Tamaño | Formato | |
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2019_Gonzalez-Soria_Alonso_AdvSynthCatal_final.pdf | Versión final (acceso restringido) | 4,45 MB | Adobe PDF | Abrir Solicitar una copia |
2019_Gonzalez-Soria_Alonso_AdvSynthCatal_revised.pdf | Versión revisada (acceso abierto) | 1,51 MB | Adobe PDF | Abrir Vista previa |
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