A Chemoenzymatic Route To Prepare Acyclic Nucleoside Analogues

dc.creatorPalazzolo, Martín Alejandro
dc.creatorNigro, Mariano José
dc.creatorIribarren, Adolfo Marcelo
dc.creatorLewkowicz, Elizabeth Sandra
dc.date.accessioned2018-04-17T21:43:23Z
dc.date.accessioned2018-11-06T14:15:15Z
dc.date.available2018-04-17T21:43:23Z
dc.date.available2018-11-06T14:15:15Z
dc.date.created2018-04-17T21:43:23Z
dc.date.issued2016-02
dc.identifierPalazzolo, Martín Alejandro; Nigro, Mariano José; Iribarren, Adolfo Marcelo; Lewkowicz, Elizabeth Sandra; A Chemoenzymatic Route To Prepare Acyclic Nucleoside Analogues; Wiley VCH Verlag; European Journal of Organic Chemistry; 2016; 5; 2-2016; 921-924
dc.identifier1434-193X
dc.identifierhttp://hdl.handle.net/11336/42399
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1884426
dc.description.abstractAcyclic nucleosides are potential antiviral and antitumor agents. In this work, their preparation through a novel chemoenzymatic procedure involving theN-alkylation of a nucleobase and subsequent aldol condensation catalyzed by a dihydroxyacetone phosphate-dependant aldolase (Rabbit Muscle Aldolase, RAMA) is described.
dc.languageeng
dc.publisherWiley VCH Verlag
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1002/ejoc.201501412
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.201501412
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectACYCLIC NUCLEOSIDES
dc.subjectBIOCATALYSIS
dc.titleA Chemoenzymatic Route To Prepare Acyclic Nucleoside Analogues
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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