Enzymatic alcoholysis of 3′,5′-di-O-acetyl-2′-deoxynucleosides-Reference-Cited by-同舟云学术

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Enzymatic alcoholysis of 3′,5′-di-O-acetyl-2′-deoxynucleosides

Published:2004-06 Issue:1-6 Volume:29 Page:129-132
ISSN:1381-1177
Container-title:Journal of Molecular Catalysis B: Enzymatic
language:en
Short-container-title:Journal of Molecular Catalysis B: Enzymatic

Author:

Zinni Marı́a A,Rodrı́guez Silvio D,Pontiggia Rodrigo M,Montserrat Javier M,Iglesias Luis E,Iribarren Adolfo M

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis

Reference17 articles.

1. Biocatalytic Selective Modifications of Conventional Nucleosides, Carbocyclic Nucleosides, and C-Nucleosides

2. Enzymatic Protecting Group Techniques

3. Regioselective deprotection of 3′,5′-O-acylated pyrimidine nucleosides by lipase and esterase

4. Regioselective Enzymatic Hydrolysis of 3′,5′-DI-O-Acetylthymidine and Observation of a Surface Effect Due to Polystyrene

5. H. Waldmann, A. Heuser, A. Reidel, Synlett (1994) 65.

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2. Synthesis of the antitumoral nucleoside capecitabine through a chemo-enzymatic approach;Tetrahedron Letters;2015-10

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4. Molecular Sieves Mediated Green Per-O-Acetylation of Carbohydrate Templates and Lipase Catalyzed Regioselective Alcoholysis of 2,3,5-Tri-O-Acetyl-D-Ribonolactone;Journal of the Brazilian Chemical Society;2015

5. Biocatalytic Methodologies for Selective Modified Nucleosides;Chemical Synthesis of Nucleoside Analogues;2013-02-15

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