Online citations, reference lists, and bibliographies.

Please confirm you are human

(Sign Up for free to never see this)

← Back to Search

DOI: 10.1007/s10529-007-9374-x

Two New Dialkoxycarbonylated Nucleosides Obtained Through A Regioselective Enzymatic Alcoholysis

Mariana Capello, Leandro Imanishi, L. Iglesias, A. Iribarren

Published 2007 · Chemistry, Medicine

Save to my Library

Download PDF

Analyze on Scholarcy

Share

Two new compounds, 2′,3′-di-O-ethoxycarbonyluridine and 2′,3′-di-O-ethoxycarbonylinosine, were obtained through a Candida antarctica lipase B catalysed regioselective ethanolysis of the corresponding trialcoxycarbonylated nucleosides with benzyl alcohol in 1,4-dioxane at 30°C.

This paper references

10.1021/CR00028A004

Enzymatic protecting group techniques.

D. Kadereit (2001)

10.1023/A:1005620617554

Complete and regioselective deacetylation of peracetylated uridines using a lipase

L. Iglesias (2004)

Hydrolases in organic chemistry, Wiley-VCH, Weinheim

U Bornscheuer (1999)

10.1021/CR000446Y

Biocatalytic selective modifications of conventional nucleosides, carbocyclic nucleosides, and C-nucleosides.

M. Ferrero (2000)

10.1016/S0040-4020(00)00671-2

Perspectives on Alkyl Carbonates in Organic Synthesis

Jay P. Parrish (2000)

10.1016/S1381-1177(99)00097-1

Lipase catalyzed reactions of aliphatic and arylaliphatic carbonic acid esters

M. Hacking (2000)

10.1016/J.MOLCATB.2005.08.001

A mild and quantitative procedure for the removal of nucleoside alkoxycarbonyl groups using pig liver esterase or Candida antarctica B lipase

Mariana Capello (2005)

10.1590/S0100-40422004000300022

Optimisation of the lipase-catalysed preparation of a nucleoside prodrug model using an experimental design methodology

María A. Zinni (2004)

Enzymatic alcoholysis of 30,50-di-O-acetyl-20-deoxynucleosides

MA Zinni (2004)

10.1023/A:1015648508146

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

María A. Zinni (2004)

10.1016/S0957-4166(00)00068-9

Resolution of a chiral alcohol through lipase-catalyzed transesterification of its mixed carbonate by poly(ethylene glycol) in organic media

Lisa J. Whalen (2000)

10.1016/J.MOLCATB.2003.11.017

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

María A. Zinni (2004)

This paper is referenced by

10.1007/978-1-61779-600-5_26

Lipases in green chemistry: acylation and alcoholysis on steroids and nucleosides.

A. Baldessari (2012)

10.1080/00397911.2018.1554745

Biocatalyst CAL-B catalyzed synthesis of modified nucleosides: An overview

R. Kumar (2019)

10.1002/9781118498088.CH1

1. Biocatalytic Methodologies for Selective Modified Nucleosides

M. Ferrero (2013)

10.1016/j.biotechadv.2010.01.006

Biocatalytic transformation of nucleoside derivatives.

Some data provided by SemanticScholar