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dc.contributor.authorSantos Ruiz, Jesús Manuel de los
dc.contributor.authorOchoa Díez, Zelai
dc.contributor.authorPalacios Gambra, Francisco Javier ORCID
dc.date.accessioned2013-07-12T10:19:25Z
dc.date.available2013-07-12T10:19:25Z
dc.date.issued2012
dc.identifier.citationARKIVOC 4: 54-62 (2012)es
dc.identifier.issn1551-7012
dc.identifier.urihttp://hdl.handle.net/10810/10413
dc.descriptionIssue in Honor of Prof. Paweł Kafarskien
dc.description.abstract[EN] The reactivity of new three carbon synthon, generated in situ from the reaction of electrondeficient allenes with an appropriate phosphine as the catalyst, toward pronucleophilic reagents is described. Triphenylphosphine-catalyzed reaction of allenes derived from phosphine oxides with nitrogen- or carbonucleophiles gave the γ-addition product as a mixture of cis and trans isomers.en
dc.language.isoengen
dc.publisherARKAT USA, Incen
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.subjectallenyl phosphine oxideen
dc.subjectphosphine catalysisen
dc.subjectpronucleophilesen
dc.subjectumpolung additionen
dc.subjectα,β-unsaturated phosphine oxidesen
dc.titleStereoselective inverse conjugate addition of nitrogen and carbon nucleophiles to allenyl phosphine oxide. Synthesis of α,β-unsaturated phosphine oxidesen
dc.typeinfo:eu-repo/semantics/articleen
dc.rights.holder© ARKAT-USA, Inc. This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 License.en
dc.relation.publisherversionhttp://quod.lib.umich.edu/cgi/p/pod/dod-idx/stereoselective-inverse-conjugate-addition-of-nitrogen.pdf?c=ark;idno=5550190.0013.406en
dc.departamentoesQuímica orgánica Ies_ES
dc.departamentoeuKimika organikoa Ies_ES


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