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

A set of eight mono-, di-, tri- and tetraalkoxycarbonylated nucleosides was tested in order to assess their enzymatic hydrolysis. All the alkoxycarbonyl groups of the assayed substrates, from both carbonate and carbamate functions, were quantitatively hydrolysed using pig liver esterase (PLE) at pH...

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Publicado: 2005
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13811177_v36_n1-6_p36_Capello
http://hdl.handle.net/20.500.12110/paper_13811177_v36_n1-6_p36_Capello
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spelling paper:paper_13811177_v36_n1-6_p36_Capello2025-07-30T18:48:06Z A mild and quantitative procedure for the removal of nucleoside alkoxycarbonyl groups using pig liver esterase or Candida antarctica B lipase Carbamates Carbonates Deprotection Hydrolases Nucleosides Enzymes Hydrolysis Substrates Synthesis (chemical) Carbamates Deprotection Hydrolases Nucleosides Carbonates carbamic acid carbonic acid carbonyl derivative esterase liver enzyme nucleoside derivative triacylglycerol lipase article Candida antarctica carbonylation catalyst controlled study hydrolysis kinetics nonhuman pH measurement quantitative analysis temperature dependence Candida antarctica Sus scrofa A set of eight mono-, di-, tri- and tetraalkoxycarbonylated nucleosides was tested in order to assess their enzymatic hydrolysis. All the alkoxycarbonyl groups of the assayed substrates, from both carbonate and carbamate functions, were quantitatively hydrolysed using pig liver esterase (PLE) at pH 7 and 60°C, regardless of the nucleoside base. Quantitative full alkoxycarbonyl groups removal was also reached by Candida antarctica B lipase (CAL B) under mild conditions, but in this case, longer reaction times were required. Thus, PLE appears as an useful catalyst for the mild and quantitative deprotection of nucleoside carbonates and carbamates in the synthesis of modified nucleosides. © 2005 Elsevier B.V. All rights reserved. 2005 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13811177_v36_n1-6_p36_Capello http://hdl.handle.net/20.500.12110/paper_13811177_v36_n1-6_p36_Capello
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Carbamates
Carbonates
Deprotection
Hydrolases
Nucleosides
Enzymes
Hydrolysis
Substrates
Synthesis (chemical)
Carbamates
Deprotection
Hydrolases
Nucleosides
Carbonates
carbamic acid
carbonic acid
carbonyl derivative
esterase
liver enzyme
nucleoside derivative
triacylglycerol lipase
article
Candida antarctica
carbonylation
catalyst
controlled study
hydrolysis kinetics
nonhuman
pH measurement
quantitative analysis
temperature dependence
Candida antarctica
Sus scrofa
spellingShingle Carbamates
Carbonates
Deprotection
Hydrolases
Nucleosides
Enzymes
Hydrolysis
Substrates
Synthesis (chemical)
Carbamates
Deprotection
Hydrolases
Nucleosides
Carbonates
carbamic acid
carbonic acid
carbonyl derivative
esterase
liver enzyme
nucleoside derivative
triacylglycerol lipase
article
Candida antarctica
carbonylation
catalyst
controlled study
hydrolysis kinetics
nonhuman
pH measurement
quantitative analysis
temperature dependence
Candida antarctica
Sus scrofa
A mild and quantitative procedure for the removal of nucleoside alkoxycarbonyl groups using pig liver esterase or Candida antarctica B lipase
topic_facet Carbamates
Carbonates
Deprotection
Hydrolases
Nucleosides
Enzymes
Hydrolysis
Substrates
Synthesis (chemical)
Carbamates
Deprotection
Hydrolases
Nucleosides
Carbonates
carbamic acid
carbonic acid
carbonyl derivative
esterase
liver enzyme
nucleoside derivative
triacylglycerol lipase
article
Candida antarctica
carbonylation
catalyst
controlled study
hydrolysis kinetics
nonhuman
pH measurement
quantitative analysis
temperature dependence
Candida antarctica
Sus scrofa
description A set of eight mono-, di-, tri- and tetraalkoxycarbonylated nucleosides was tested in order to assess their enzymatic hydrolysis. All the alkoxycarbonyl groups of the assayed substrates, from both carbonate and carbamate functions, were quantitatively hydrolysed using pig liver esterase (PLE) at pH 7 and 60°C, regardless of the nucleoside base. Quantitative full alkoxycarbonyl groups removal was also reached by Candida antarctica B lipase (CAL B) under mild conditions, but in this case, longer reaction times were required. Thus, PLE appears as an useful catalyst for the mild and quantitative deprotection of nucleoside carbonates and carbamates in the synthesis of modified nucleosides. © 2005 Elsevier B.V. All rights reserved.
title A mild and quantitative procedure for the removal of nucleoside alkoxycarbonyl groups using pig liver esterase or Candida antarctica B lipase
title_short A mild and quantitative procedure for the removal of nucleoside alkoxycarbonyl groups using pig liver esterase or Candida antarctica B lipase
title_full A mild and quantitative procedure for the removal of nucleoside alkoxycarbonyl groups using pig liver esterase or Candida antarctica B lipase
title_fullStr A mild and quantitative procedure for the removal of nucleoside alkoxycarbonyl groups using pig liver esterase or Candida antarctica B lipase
title_full_unstemmed A mild and quantitative procedure for the removal of nucleoside alkoxycarbonyl groups using pig liver esterase or Candida antarctica B lipase
title_sort mild and quantitative procedure for the removal of nucleoside alkoxycarbonyl groups using pig liver esterase or candida antarctica b lipase
publishDate 2005
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13811177_v36_n1-6_p36_Capello
http://hdl.handle.net/20.500.12110/paper_13811177_v36_n1-6_p36_Capello
_version_ 1840326492979986432