Enzymatic Regioselective Alkoxycarbonylation of Nucleosides and Its Utility in Nucleoside Derivative Synthesis

التفاصيل البيبلوغرافية
العنوان: Enzymatic Regioselective Alkoxycarbonylation of Nucleosides and Its Utility in Nucleoside Derivative Synthesis
المؤلفون: Luis F. García-Alles, Francisco Morís, Vicente Gotor
المساهمون: Universidad de Oviedo [Oviedo], Universidad de Oviedo
المصدر: Biocatalysis and Agricultural Biotechnology
Biocatalysis and Agricultural Biotechnology, 2009, 10 (1-4), pp.295-305. ⟨10.3109/10242429409065239⟩
بيانات النشر: HAL CCSD, 2009.
سنة النشر: 2009
مصطلحات موضوعية: chemistry.chemical_classification, [SDV.BIO]Life Sciences [q-bio]/Biotechnology, 010405 organic chemistry, Regioselectivity, 010402 general chemistry, 01 natural sciences, Biochemistry, Catalysis, 0104 chemical sciences, chemistry.chemical_compound, Enzyme, chemistry, Organic chemistry, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology, General Agricultural and Biological Sciences, Nucleoside, Derivative (chemistry), ComputingMilieux_MISCELLANEOUS, Biotechnology
الوصف: The regioselective enzymatic alkoxycarbonylation of nucleosides is described for α-, xylo-, anhydro-, and arabino-nucleosides to obtain Cbz-derivatives. The utility of these compounds and of the related vinyl carbonates of 2‘-deoxynucleosides is shown by the synthesis of 3‘-O-acetates of α-and xylo-thymidine and the synthesis of some nucleoside carbamates, respectively.
اللغة: English
تدمد: 1878-8181
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::294ca0b424ba7e035a6385b1ae94680fTest
https://hal.insa-toulouse.fr/hal-03367262Test
رقم الانضمام: edsair.doi.dedup.....294ca0b424ba7e035a6385b1ae94680f
قاعدة البيانات: OpenAIRE