dc.creatorDella Felice, Franco
dc.creatorSarotti, Ariel Marcelo
dc.creatorPilli, Ronaldo A.
dc.date.accessioned2018-07-26T19:13:31Z
dc.date.accessioned2018-11-06T16:01:44Z
dc.date.available2018-07-26T19:13:31Z
dc.date.available2018-11-06T16:01:44Z
dc.date.created2018-07-26T19:13:31Z
dc.date.issued2017-09
dc.identifierDella Felice, Franco; Sarotti, Ariel Marcelo; Pilli, Ronaldo A.; Catalytic Asymmetric Synthesis and Stereochemical Revision of (+)-Cryptoconcatone H; American Chemical Society; Journal of Organic Chemistry; 82; 17; 9-2017; 9191-9197
dc.identifier0022-3263
dc.identifierhttp://hdl.handle.net/11336/53198
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1903697
dc.description.abstractThe total synthesis and structural revision of (+)-cryptoconcatone H are described. Guided by computational studies for the final structure assignment, the stereogenic centers at the tetrahydropyran moiety of (+)-cryptoconcatone H were assembled through catalytic asymmetric methodologies: Krische allylation, cross-metathesis reaction, and THP formation via Pd(II)-catalyzed cyclization. Finally, a Krische allylation reaction established the last stereocenter, and the lactone moiety was formed by ring-closing metathesis.
dc.languageeng
dc.publisherAmerican Chemical Society
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1021/acs.joc.7b01378
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acs.joc.7b01378
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCATALYTIC ASYMMETRIC SYNTHESIS
dc.subjectSTEREOCHEMICAL REVISION
dc.subjectCRYPTOCONCATONE H
dc.subjectDP4+ CALCULATIONS
dc.titleCatalytic Asymmetric Synthesis and Stereochemical Revision of (+)-Cryptoconcatone H
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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