dc.creatorVargas Vargas, Didier Farley
dc.creatorLarghi, Enrique Leandro
dc.creatorKaufman, Teodoro Saul
dc.date.accessioned2020-06-23T20:40:34Z
dc.date.accessioned2022-10-15T14:25:31Z
dc.date.available2020-06-23T20:40:34Z
dc.date.available2022-10-15T14:25:31Z
dc.date.created2020-06-23T20:40:34Z
dc.date.issued2018-08
dc.identifierVargas Vargas, Didier Farley; Larghi, Enrique Leandro; Kaufman, Teodoro Saul; The 6π-azaelectrocyclization of azatrienes: Synthetic applications in natural products, bioactive heterocycles, and related fields; Royal Society of Chemistry; Natural Product Reports; 36; 2; 8-2018; 354-401
dc.identifier0265-0568
dc.identifierhttp://hdl.handle.net/11336/108032
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4396632
dc.description.abstractThe application of the 6p-azaelectrocyclization of azatrienes as a key strategy for the synthesis of natural products, their analogs and related bioactive or biomedically-relevant compounds (from 2006 to date) iscomprehensively reviewed. Details about reaction optimization studies, relevant reaction mechanisms and conditions are also discussed.
dc.languageeng
dc.publisherRoyal Society of Chemistry
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2019/np/c8np00014j#!divAbstract
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/c8np00014j
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subject6π-AZAELECTROCYCLIZATION
dc.subjectAZATRIENES
dc.subjectNATURAL PRODUCTS
dc.subjectBIOACTIVE HETEROCYCLES
dc.titleThe 6π-azaelectrocyclization of azatrienes: Synthetic applications in natural products, bioactive heterocycles, and related fields
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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