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dc.contributor.author | Mastachi Loza, Salvador | |
dc.contributor.author | Ramírez Candelero, Tania Ivonne | |
dc.contributor.author | González Romero, Carlos | |
dc.contributor.author | Díaz Torres, Eduardo | |
dc.contributor.author | Fuentes Benítes, Aydeé | |
dc.contributor.author | Tamariz, Joaquín | |
dc.date.accessioned | 2018-11-07T18:49:28Z | |
dc.date.available | 2018-11-07T18:49:28Z | |
dc.date.issued | 2018-10-19 | |
dc.identifier.issn | 2193-5815 | |
dc.identifier.uri | http://hdl.handle.net/20.500.11799/95034 | |
dc.description | En este documento se detalla con profundidad la reactividad de los dienos exo-heterocíclicos frente a dienófilos tales chalconas y compuestos 1,3-dicarbonílicos | es |
dc.description.abstract | The N-substituted exo-2-oxazolidinone dienes are versatile molecules that undergo a variety of reactions. To further explore this versatility, Diels-Alder reactions were carried out with novel naphthalene chalcones. Upon attempting the Diels-Alder reaction with 2-hydroxy-1,4-naphthoquinone, the formation of chromene unexpectedly took place via a formal [3+3] cycloaddition reaction. The observed reaction was then achieved with other 1,3-dicarbonyl compounds | es |
dc.description.sponsorship | Secretaría de Investigación y Estudios Avanzados de la Universidad Autónoma del Estado de México | es |
dc.language.iso | eng | es |
dc.publisher | Asian Journal of Organic Chemistry | es |
dc.rights | embargoedAccess | es |
dc.rights | https://creativecommons.org/licenses/by/4.0/ | es |
dc.rights | embargoedAccess | es |
dc.rights | https://creativecommons.org/licenses/by/4.0/ | es |
dc.subject | Exo-oxazolidin-2-one | es |
dc.subject | Naphthalene Chalcones | es |
dc.subject | 1,3-Dicarbonyl Compounds | es |
dc.subject | Research Subject Categories::NATURAL SCIENCES | es |
dc.title | Reactivity of N‐substituted Exo‐oxazolidin‐2‐one Dienes with Naphthalene Chalcones and Cyclic 1,3‐Dicarbonyl Compounds | es |
dc.type | Artículo | es |
dc.provenance | Científica | es |
dc.road | Dorada | es |
dc.organismo | Química | es |
dc.ambito | Internacional | es |
dc.cve.CenCos | 20401 | es |
dc.cve.progEstudios | 724 | es |