Nucleoside N-acylation with active derivatives of amino acids
Simple procedure for N-acylation ofadenosine guanosine and cytidine by active derivatives of amino acids is proposed. Procedure is based on transient silyt protection ofribose hydroxy groups and consists of 3 steps: (a) silytotion of nucleoside by trimethylchloro-silane, (b) reaction of amino group...
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| Datum: | 1996 |
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| Hauptverfasser: | , , , |
| Format: | Artikel |
| Sprache: | English |
| Veröffentlicht: |
Інститут молекулярної біології і генетики НАН України
1996
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| Schriftenreihe: | Биополимеры и клетка |
| Online Zugang: | https://nasplib.isofts.kiev.ua/handle/123456789/154168 |
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| Назва журналу: | Digital Library of Periodicals of National Academy of Sciences of Ukraine |
| Zitieren: | Nucleoside N-acylation with active derivatives of amino acids / S.M. Yarmoluk, A.M. Kostenko, D.V. Kryvorotenko, I.Y. Dubey // Биополимеры и клетка. — 1996. — Т. 12, № 5. — С. 50-55. — Бібліогр.: 9 назв. — англ. |
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Digital Library of Periodicals of National Academy of Sciences of Ukraine| Zusammenfassung: | Simple procedure for N-acylation ofadenosine guanosine and cytidine by active derivatives of amino acids is proposed. Procedure is based on transient silyt protection ofribose hydroxy groups and consists of 3 steps: (a) silytotion of nucleoside by trimethylchloro-silane, (b) reaction of amino group ofsilylated nucleoside with chloroanhydride or active ester of N-protected amino acid, (c) desilylation of intermediate. The yields of N-amino-acylated nucleosides were about 40–90 %. |
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