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Chemoenzymatic synthesis of optically active phenolic 3,4-dihydropyridin-2-ones: A way to access enantioenriched 1,4-dihydropyridine and benzodiazepine derivatives

dc.contributor.authorTorres Nieto, Susana Yanet
dc.contributor.authorBrieva Collado, María del Rosario 
dc.contributor.authorRebolledo Vicente, Francisca 
dc.date.accessioned2017-12-14T11:04:10Z
dc.date.available2017-12-14T11:04:10Z
dc.date.issued2017
dc.identifier.citationOrganic and Biomolecular Chemistry, 15(24), p. 5171-5181 (2017); doi:10.1039/c7ob01066d
dc.identifier.issn1477-0520
dc.identifier.urihttp://hdl.handle.net/10651/44917
dc.description.sponsorshipMAEC, Ministerio de Asuntos Exteriores y de Cooperación
dc.description.sponsorshipThis work was supported by the Ministerio de Ciencia e Innovation of Spain (Project CTQ 2014-55015) and Principado de Asturias (FC-15-GRUPIN14-002). S. Y. T. thanks to the Spanish MAEC for a grant (MAEC-AECID program)
dc.format.extentp. 5171-5181
dc.language.isoeng
dc.relation.ispartofOrganic and Biomolecular Chemistry
dc.rights©,
dc.sourceScopus
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85021655869&doi=10.1039%2fc7ob01066d&partnerID=40&md5=784b39d5847eb2c83141dad423af1aa1
dc.titleChemoenzymatic synthesis of optically active phenolic 3,4-dihydropyridin-2-ones: A way to access enantioenriched 1,4-dihydropyridine and benzodiazepine derivatives
dc.typejournal article
dc.identifier.doi10.1039/c7ob01066d
dc.relation.projectIDCTQ 2014-55015
dc.relation.projectIDFC-15-GRUPIN14-002
dc.relation.projectIDMAEC-AECID program
dc.relation.publisherversionhttp://dx.doi.org/10.1039/c7ob01066d


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