Synthesis of branched arabinofuranose pentasaccharide fragment of mycobacterial arabinans as 2-azidoethyl glycoside Full article
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Carbohydrate Research
ISSN: 1873-426X , E-ISSN: 0008-6215 |
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| Output data | Year: 2012, Volume: 357, Pages: 62-67 Pages count : 6 DOI: 10.1016/j.carres.2012.05.021 | ||||
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Abstract:
Branched arabinofuranose pentasaccharide with 2-azidoethyl aglycon was prepared for the first time by [3+1+1] bis-(1,2-cis)-glycosylation of trisaccharide diol with silyl-protected thioglycoside glycosyl donor. The presence of 2-azidoethyl aglycon would enable the preparation of neoglycoconjugates using the click chemistry approaches.
Cite:
Fedina K.G.
, Abronina P.I.
, Podvalnyy N.M.
, Kondakov N.N.
, Chizhov A.O.
, Torgov V.I.
, Kononov L.O.
Synthesis of branched arabinofuranose pentasaccharide fragment of mycobacterial arabinans as 2-azidoethyl glycoside
Carbohydrate Research. 2012. V.357. P.62-67. DOI: 10.1016/j.carres.2012.05.021 WOS Scopus OpenAlex
Synthesis of branched arabinofuranose pentasaccharide fragment of mycobacterial arabinans as 2-azidoethyl glycoside
Carbohydrate Research. 2012. V.357. P.62-67. DOI: 10.1016/j.carres.2012.05.021 WOS Scopus OpenAlex
Identifiers:
| Web of science: | WOS:000306273700008 |
| Scopus: | 2-s2.0-84863724268 |
| OpenAlex: | W2032185163 |