Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Elena V. Zhernosek"'
Autor:
Elena V. Zhernosek, A. I. Zinchenko, Sergei V. Kvach, Ludmilla A. Eroshevskaya, Elena N. Kalinichenko
Publikováno v:
Chemistry of Natural Compounds. 42:208-211
Previously undescribed conjugates of 2′,3′-dideoxyuridine-5′-monophosphate-(L)-methoxytryptophylphosphoramidate (5) and 2′,3′-dideoxycytidine-5′-monophosphate-(L)-methoxytryptophylphosphoramidate (7) were isolated by a chemical enzymatic
Autor:
Erik De Clercq, Igor A. Mikhailopulo, A. I. Zinchenko, Vladimir N. Barai, Ludmilla A. Eroshevskaya, Elena V. Zhernosek, Jan Balzarini
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 22:751-753
9-(3-Deoxy-beta-D-erythro-pentofuranosyl)-2,6-diaminopurine (2) was synthesized by an enzymatic transglycosylation of 2,6-diaminopurine using 3'-deoxycytidine (1) as a donor of the sugar moiety. Nucleoside 2 was transformed to 3'-deoxy guanosine (3),
Publikováno v:
Synthesis. 2002
A practical synthesis of peracylated derivatives of β-L-ribofuranose 13-15 from D-ribose was accomplished in 6 steps (total yield: 30-45% Compound 13 was employed for the preparation of 1-(β-L-ribofuranosyl)thymine (16) and -cytosine (17), which ar
Autor:
Vladimir N. Barai, Elena V. Zhernosek, Ludmilla A. Eroshevskaya, A. I. Zinchenko, Igor A. Mikhailopulo, Erik De Clercq
Publikováno v:
Helvetica Chimica Acta. 85:1893
9-(3-Deoxy-β-D-erythro-pentofuranosyl)-2,6-diaminopurine (6) was synthesized by an enzymatic transglycosylation of 2,6-diaminopurine (2) with 3′-deoxycytidine (1) as a donor of 3-deoxy-D-erythro-pentofuranose moiety. This transformation comprises