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Approaches to intramolecular sialylation. 3. Synthesis of 2,4-dimethoxybenzyl ester of per-O-acetylated N-acetylneuraminic acid thioglycoside and its attempted oxidation with DDQ in the presence of nucleophiles Full article

Journal Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Output data Year: 2004, Volume: 53, Number: 1, Pages: 254-258 Pages count : 5 DOI: 10.1023/b:rucb.0000024859.13495.0e
Authors Kononov L.O. 1 , Malysheva N.N. 1 , Ito Y. 2 , Ogawa T. 2
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation
2 Institute of Physical and Chemical Research (RIKEN), Hirosawa 2-1, Wako-shi, Saitama, 351-01, Japan

Abstract: 2,4-Dimethoxybenzyl ester of per-O-acetylated N-acetylneuraminic acid thioglycoside was synthesized and attempts at the oxidative (DDQ-induced) addition of O-nucleophiles (water and galactose derivatives with unprotected hydroxy group at C(6)) to the benzylic carbon atom of this ester were made.
Cite: Kononov L.O. , Malysheva N.N. , Ito Y. , Ogawa T.
Approaches to intramolecular sialylation. 3. Synthesis of 2,4-dimethoxybenzyl ester of per-O-acetylated N-acetylneuraminic acid thioglycoside and its attempted oxidation with DDQ in the presence of nucleophiles
Russian Chemical Bulletin. 2004. V.53. N1. P.254-258. DOI: 10.1023/b:rucb.0000024859.13495.0e WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000221151700038
Scopus: 2-s2.0-3442878941
OpenAlex: W2953119616
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Scopus 3
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