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A Novel Glycosyl Donor with a Triisopropylsilyl Nonparticipating Group in Benzyl-Free Stereoselective 1,2-cis-Galactosylation
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V.28. N13. P.1608-1613. DOI: 10.1055/s-0036-1589028
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Russian Chemical Bulletin. 2017.
V.66. N11. P.2173-2179. DOI: 10.1007/s11172-017-1999-x
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Stereoselective sialylation with O-trifluoroacetylated thiosialosides: hydrogen bonding involved?
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Russian Chemical Bulletin. 2017.
V.66. N9. P.1712-1715. DOI: 10.1007/s11172-017-1945-y
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An efficient multigram-scale synthesis of 4-(ω-chloroalkoxy)phenols
Russian Chemical Bulletin. 2017.
V.66. N2. P.304-312. DOI: 10.1007/s11172-017-1732-9
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Rapid synthesis of linear homologous oligoarabinofuranosides related to mycobacterial lipoarabinomannan and a neoglycoconjugate thereof
Carbohydrate Research. 2016.
V.431. P.25-32. DOI: 10.1016/j.carres.2016.05.009
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Glycosylation of dibutyl phosphate anion with arabinofuranosyl bromide: unusual influence of concentration of the reagents on the ratio of anomeric glycosyl phosphates formed
Russian Chemical Bulletin. 2016.
V.65. N11. P.2776-2778. DOI: 10.1007/s11172-016-1654-y
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Syntheses of O-antigen polysaccharide fragments of nitrogen-fixing rhizobacteria of the genus Azospirillum
Russian Chemical Bulletin. 2016.
V.65. N6. P.1448-1463. DOI: 10.1007/s11172-016-1472-2
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V.71. N14. P.1392-1396. DOI: 10.1134/s1061934816140045
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V.26. N16. P.2267-2271. DOI: 10.1055/s-0035-1560172
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Synthesis of a disaccharide of phenolic glycolipid from Mycobacterium leprae (PGL-I) and its conjugates with bovine serum albumin
Russian Chemical Bulletin. 2015.
V.64. N5. P.1142-1148. DOI: 10.1007/s11172-015-0991-6
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Russian Chemical Bulletin. 2015.
V.64. N5. P.1149-1162. DOI: 10.1007/s11172-015-0992-5
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V.70. N14. P.1664-1670. DOI: 10.1134/s106193481514004x
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Glysosylation of nucleophiles on ion-exchange resin: a new synthesis of dibenzyl glycosyl phosphates
Russian Chemical Bulletin. 2015.
V.64. N5. P.1202-1204. DOI: 10.1007/s11172-015-1002-7
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Russian Chemical Bulletin. 2014.
V.63. N1. P.295-297. DOI: 10.1007/s11172-014-0429-6
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Synthesis of 3,6-di-O-methyl-β-d-glucopyranose conjugates
Russian Chemical Bulletin. 2014.
V.63. N2. P.501-506. DOI: 10.1007/s11172-014-0460-7
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V.63. N2. P.497-500. DOI: 10.1007/s11172-014-0459-0
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