Complete and regioselective deacetylation of peracetylated uridines using a lipase

dc.creatorIglesias, Luis Emilio
dc.creatorZinni, Maria Alejandra
dc.creatorGallo, Mariana
dc.creatorIribarren, Adolfo Marcelo
dc.date.accessioned2019-03-14T18:45:59Z
dc.date.accessioned2022-10-15T11:03:12Z
dc.date.available2019-03-14T18:45:59Z
dc.date.available2022-10-15T11:03:12Z
dc.date.created2019-03-14T18:45:59Z
dc.date.issued2000-01
dc.identifierIglesias, Luis Emilio; Zinni, Maria Alejandra; Gallo, Mariana; Iribarren, Adolfo Marcelo; Complete and regioselective deacetylation of peracetylated uridines using a lipase; Springer; Biotechnology Letters; 22; 5; 1-2000; 361-365
dc.identifier0141-5492
dc.identifierhttp://hdl.handle.net/11336/71667
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4378656
dc.description.abstractLipase-catalysed alcoholysis and hydrolysis of 2',3',5-tri-O- acetyluridine (1a) and 2',3',5'-tri-O-acetyl-2'-C-methyluridine (1b) were studied. Conditions for full and regioselective deacetylation of 1a and 1b are shown in the present work. New compound 2',3'-di-O-acetyl-2'-C- methyluridine (3b) was prepared by regioselective lipase-catalysed deacetylation.
dc.languageeng
dc.publisherSpringer
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1023/A:1005620617554
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1023/A:1005620617554
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectACETYLURIDINES
dc.subjectDEACETYLATION
dc.subjectLIPASE
dc.subjectNUCLEOSIDES
dc.subjectTRIACETYLURIDINES
dc.titleComplete and regioselective deacetylation of peracetylated uridines using a lipase
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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