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The use of O-trifluoroacetyl protection and profound influence of the nature of glycosyl acceptor in benzyl-free arabinofuranosylation.
Carbohydr Res. 2014 Sep 19;396:25-36. doi: 10.1016/j.carres.2014.05.017. Epub 2014 Jun 5.
Carbohydr Res. 2014.
PMID: 25079596
Ring opening of acylated β-d-arabinofuranose 1,2,5-orthobenzoates with nucleophiles allows access to novel selectively-protected arabinofuranose building blocks.
Podvalnyy NM, Sedinkin SL, Abronina PI, Zinin AI, Fedina KG, Torgov VI, Kononov LO.
Podvalnyy NM, et al. Among authors: fedina kg.
Carbohydr Res. 2011 Jan 3;346(1):7-15. doi: 10.1016/j.carres.2010.11.002. Epub 2010 Nov 5.
Carbohydr Res. 2011.
PMID: 21109236
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Synthesis of branched arabinofuranose pentasaccharide fragment of mycobacterial arabinans as 2-azidoethyl glycoside.
Fedina KG, Abronina PI, Podvalnyy NM, Kondakov NN, Chizhov AO, Torgov VI, Kononov LO.
Fedina KG, et al.
Carbohydr Res. 2012 Aug 1;357:62-7. doi: 10.1016/j.carres.2012.05.021. Epub 2012 May 28.
Carbohydr Res. 2012.
PMID: 22704193
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Bimodal concentration-dependent reactivity pattern of a glycosyl donor: Is the solution structure involved?
Kononov LO, Fedina KG, Orlova AV, Kondakov NN, Abronina PI, Podvalnyy NM, Chizhov AO.
Kononov LO, et al. Among authors: fedina kg.
Carbohydr Res. 2017 Jan 2;437:28-35. doi: 10.1016/j.carres.2016.11.009. Epub 2016 Nov 12.
Carbohydr Res. 2017.
PMID: 27883907
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