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dc.contributor.author | ZARAGOZA GALICIA, IVANN | |
dc.contributor.author | SANTOS SANCHEZ, ZAIRA ARGELIA | |
dc.contributor.author | Hidalgo Mercado, Yazmín Itzel | |
dc.contributor.author | Olivo, Horacio | |
dc.contributor.author | ROMERO ORTEGA, MOISES | |
dc.creator | ZARAGOZA GALICIA, IVANN; 231282 | |
dc.creator | SANTOS SANCHEZ, ZAIRA ARGELIA; 642259 | |
dc.creator | Hidalgo Mercado, Yazmín Itzel;x1350207 | |
dc.creator | Olivo, Horacio;#0000-0002-8082-5285 | |
dc.creator | ROMERO ORTEGA, MOISES; 14987 | |
dc.date.accessioned | 2019-11-04T23:47:26Z | |
dc.date.available | 2019-11-04T23:47:26Z | |
dc.date.issued | 2019-10-08 | |
dc.identifier.issn | 0039-7881 | |
dc.identifier.uri | http://hdl.handle.net/20.500.11799/104783 | |
dc.description | En el presente trabajo se describe un procedimiento simple y fácil para la preparación de pirrolidinonas 5-sustituidas a partir de un acoplamiento entre iones N-aciliminio y reactivos organometálicos derivados de zinc | es |
dc.description.abstract | A coupling reaction between cyclic N-acyliminium ions with organozinc reagents is described. The cyclic N-acyliminium ions, generated in situ from N-substituted-5-hydroxy-2-pyrrolidinones by treatment with BF3-etherate or titanium tetrachloride, were trapped by the organozinc reagent, formed by the alkylbromide in the presence of zinc in the same reaction media. The N-substituted 5-allyl-2-pyrrolidinones generated using this method, serves as versatile intermediates for the synthesis of azabicyclic systems with indolizidine and pyrroloazepinolizidine cores. | es |
dc.language.iso | eng | es |
dc.publisher | Thieme | es |
dc.rights | openAccess | es |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0 | |
dc.subject | Synthesis of 5-Substituted-2-pyrrolidinones by coupling of organozinc reagents with cyclic N-acyliminium ions | es |
dc.subject.classification | BIOLOGÍA Y QUÍMICA | |
dc.title | Synthesis of 5-substituted 2-pyrrolidinones by coupling of organozinc reagents with cyclic N-acyliminium ions | 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 | 57 | es |
dc.audience | students | es |
dc.audience | researchers | es |
dc.type.conacyt | article | |
dc.identificator | 2 |