Cycloisomerization of Conjugated Trienones and Isomeric 2 H -Pyrans: Unified Strategy toward Cyclopenta[ b ]furans

dc.creatorRiveira, Martín Jorge
dc.creatorQuiroga, Gastón N.
dc.creatorMata, Ernesto Gabino
dc.creatorGandon, Vincent
dc.creatorMischne, Mirta Paulina
dc.date.accessioned2018-07-03T18:23:30Z
dc.date.accessioned2018-11-06T14:04:05Z
dc.date.available2018-07-03T18:23:30Z
dc.date.available2018-11-06T14:04:05Z
dc.date.created2018-07-03T18:23:30Z
dc.date.issued2015-06
dc.identifierRiveira, Martín Jorge; Quiroga, Gastón N.; Mata, Ernesto Gabino; Gandon, Vincent; Mischne, Mirta Paulina; Cycloisomerization of Conjugated Trienones and Isomeric 2 H -Pyrans: Unified Strategy toward Cyclopenta[ b ]furans; American Chemical Society; Journal of Organic Chemistry; 80; 12; 6-2015; 6515-6519
dc.identifier0022-3263
dc.identifierhttp://hdl.handle.net/11336/51063
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1882502
dc.description.abstractConjugated trienones and isomeric 2H-pyrans were found to engage in a novel cycloisomerization cascade toward cyclopenta[b]furan derivatives. Knoevenagel chemistry and pericyclic reactions meet again to expand the polyene-carbonyl manifold.
dc.languageeng
dc.publisherAmerican Chemical Society
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/acs.joc.5b00818
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acs.joc.5b00818
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCycloisomerization
dc.subjectcyclopenta[b]furan derivatives
dc.titleCycloisomerization of Conjugated Trienones and Isomeric 2 H -Pyrans: Unified Strategy toward Cyclopenta[ b ]furans
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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