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dc.contributor.authorÁlvarez Bercedo, Paula
dc.contributor.authorFalomir, Eva
dc.contributor.authorMurga, Juan
dc.contributor.authorCarda, Miguel
dc.contributor.authorMarco, J. Alberto
dc.date.accessioned2011-05-12T10:28:59Z
dc.date.available2011-05-12T10:28:59Z
dc.date.issued2008-08
dc.identifier.citationÁLVAREZ BERCEDO, Laura; FALOMIR, Eva; MURGA, Juan; CARDA, Miguel; MARCO, J. Alberto. Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine. European journal of organic chemistry, 2008, no. 23, p. 4015-4018
dc.identifier.issn1434-193X
dc.identifier.urihttp://hdl.handle.net/10234/22304
dc.description.abstractThe first total synthesis of the naturally occurring dihydropyranone dodoneine is reported. Asymmetric allylations were used for the stereoselective generation of the two stereogenic centers. The pyranone ring was created by means of a ringclosing metathesis
dc.format.extent5 p.
dc.language.isoeng
dc.publisherWiley-VCH
dc.relation.isPartOfEuropean journal of organic chemistry, 2008, no. 23
dc.rights.urihttp://rightsstatements.org/vocab/CNE/1.0/*
dc.subjectDodoneine
dc.subjectOxygen heterocycles
dc.subject5,6-Dihydropyran-2-ones
dc.subjectAllylation
dc.subjectAsymmetric synthesis
dc.subjectRing-closing metathesis
dc.titleStereoselective synthesis of the naturally occurring 2-pyranone dodoneine
dc.typeinfo:eu-repo/semantics/article
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess


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