Regioselective preparation of 2′, 3′-di-O-acylribonucleosides carrying lipophilic acyl groups through a lipase-catalysed alcoholysis

Biotechnology Letters

Volumn 24, Issue 12, 2002, Pages 979-983

  Zinni, María A ^a   Iglesias, Luis E ^a   Iribarren, Adolfo M ^a,b  

^a UNIVERSIDAD NACIONAL DE QUILMES   (Argentina)

^b INSTITUTO DE INVESTIGACIONES EN INGENIERÍA GENÉTICA Y BIOLOGÍA MOLECULAR   (Argentina)

Author keywords

2 , 3 di O acylribonucleosides; Deacylation; Enzymatic alcoholysis; Lipases; Nucleosides

Indexed keywords

2',3' DI O ACYLRIBONUCLEOSIDE; 2',3' DI O DODECANOYLINOSINE; 2',3' DI O DODECANOYLURIDINE; 2',3' DI O HEXANOYLINOSINE; 2',3' DI O HEXANOYLURIDINE; 2',3',5' TRI O DODECANOYLINOSINE; 2',3',5' TRI O DODECANOYLURIDINE; 2',3',5' TRI O HEXANOYLINOSINE; 2',3',5' TRI O HEXANOYLURIDINE; ANTIVIRUS AGENT; INOSINE DERIVATIVE; NUCLEOSIDE ANALOG; RIBONUCLEOSIDE DERIVATIVE; UNCLASSIFIED DRUG; URIDINE DERIVATIVE;

ACYLATION; ANTIVIRAL ACTIVITY; ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CONTROLLED STUDY; ENZYME ACTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROLYSIS; LIPOPHILICITY; NONHUMAN; THIN LAYER CHROMATOGRAPHY;

CANDIDA; CANDIDA ANTARCTICA;

EID: 0036084565     PISSN: 01415492     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1015648508146     Document Type: Article

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