Two new dialkoxycarbonylated nucleosides obtained through a regioselective enzymatic alcoholysis
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. © 2007 Springer Scienc...
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| Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_01415492_v29_n8_p1217_Capello |
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todo:paper_01415492_v29_n8_p1217_Capello2023-10-03T14:58:41Z Two new dialkoxycarbonylated nucleosides obtained through a regioselective enzymatic alcoholysis Capello, M. Imanishi, L. Iglesias, L.E. Iribarren, A.M. Carbonates Enzymatic alcoholysis Lipases Nucleosides Benzyl alcohol Enzymatic alcoholysis Nucleosides Regioselective ethanolysis Alcohols Carbonates Catalysis Enzyme activity Lipases Regioselectivity Nucleotides 1,4-dioxane alcohol derivative dioxane dioxane derivative enzyme lipase B, Candida antarctica nucleoside triacylglycerol lipase unclassified drug article biology Candida catalysis chemical model chemistry enzyme specificity enzymology methodology stereoisomerism temperature Alcohols Candida Catalysis Computational Biology Dioxanes Enzymes Lipase Models, Chemical Nucleosides Stereoisomerism Substrate Specificity Temperature Candida antarctica 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. © 2007 Springer Science+Business Media B.V. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_01415492_v29_n8_p1217_Capello |
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Universidad de Buenos Aires |
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I-28 |
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R-134 |
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Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
Carbonates Enzymatic alcoholysis Lipases Nucleosides Benzyl alcohol Enzymatic alcoholysis Nucleosides Regioselective ethanolysis Alcohols Carbonates Catalysis Enzyme activity Lipases Regioselectivity Nucleotides 1,4-dioxane alcohol derivative dioxane dioxane derivative enzyme lipase B, Candida antarctica nucleoside triacylglycerol lipase unclassified drug article biology Candida catalysis chemical model chemistry enzyme specificity enzymology methodology stereoisomerism temperature Alcohols Candida Catalysis Computational Biology Dioxanes Enzymes Lipase Models, Chemical Nucleosides Stereoisomerism Substrate Specificity Temperature Candida antarctica |
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Carbonates Enzymatic alcoholysis Lipases Nucleosides Benzyl alcohol Enzymatic alcoholysis Nucleosides Regioselective ethanolysis Alcohols Carbonates Catalysis Enzyme activity Lipases Regioselectivity Nucleotides 1,4-dioxane alcohol derivative dioxane dioxane derivative enzyme lipase B, Candida antarctica nucleoside triacylglycerol lipase unclassified drug article biology Candida catalysis chemical model chemistry enzyme specificity enzymology methodology stereoisomerism temperature Alcohols Candida Catalysis Computational Biology Dioxanes Enzymes Lipase Models, Chemical Nucleosides Stereoisomerism Substrate Specificity Temperature Candida antarctica Capello, M. Imanishi, L. Iglesias, L.E. Iribarren, A.M. Two new dialkoxycarbonylated nucleosides obtained through a regioselective enzymatic alcoholysis |
| topic_facet |
Carbonates Enzymatic alcoholysis Lipases Nucleosides Benzyl alcohol Enzymatic alcoholysis Nucleosides Regioselective ethanolysis Alcohols Carbonates Catalysis Enzyme activity Lipases Regioselectivity Nucleotides 1,4-dioxane alcohol derivative dioxane dioxane derivative enzyme lipase B, Candida antarctica nucleoside triacylglycerol lipase unclassified drug article biology Candida catalysis chemical model chemistry enzyme specificity enzymology methodology stereoisomerism temperature Alcohols Candida Catalysis Computational Biology Dioxanes Enzymes Lipase Models, Chemical Nucleosides Stereoisomerism Substrate Specificity Temperature Candida antarctica |
| description |
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. © 2007 Springer Science+Business Media B.V. |
| format |
JOUR |
| author |
Capello, M. Imanishi, L. Iglesias, L.E. Iribarren, A.M. |
| author_facet |
Capello, M. Imanishi, L. Iglesias, L.E. Iribarren, A.M. |
| author_sort |
Capello, M. |
| title |
Two new dialkoxycarbonylated nucleosides obtained through a regioselective enzymatic alcoholysis |
| title_short |
Two new dialkoxycarbonylated nucleosides obtained through a regioselective enzymatic alcoholysis |
| title_full |
Two new dialkoxycarbonylated nucleosides obtained through a regioselective enzymatic alcoholysis |
| title_fullStr |
Two new dialkoxycarbonylated nucleosides obtained through a regioselective enzymatic alcoholysis |
| title_full_unstemmed |
Two new dialkoxycarbonylated nucleosides obtained through a regioselective enzymatic alcoholysis |
| title_sort |
two new dialkoxycarbonylated nucleosides obtained through a regioselective enzymatic alcoholysis |
| url |
http://hdl.handle.net/20.500.12110/paper_01415492_v29_n8_p1217_Capello |
| work_keys_str_mv |
AT capellom twonewdialkoxycarbonylatednucleosidesobtainedthrougharegioselectiveenzymaticalcoholysis AT imanishil twonewdialkoxycarbonylatednucleosidesobtainedthrougharegioselectiveenzymaticalcoholysis AT iglesiasle twonewdialkoxycarbonylatednucleosidesobtainedthrougharegioselectiveenzymaticalcoholysis AT iribarrenam twonewdialkoxycarbonylatednucleosidesobtainedthrougharegioselectiveenzymaticalcoholysis |
| _version_ |
1807322934282289152 |