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Protecting-group- and microwave-free synthesis of β-glycosyl esters and aryl β-glycosides of N-acetyl-d-glucosamine.
Bioorg Med Chem. 2022 Aug 1;67:116852. doi: 10.1016/j.bmc.2022.116852. Epub 2022 May 25.
Bioorg Med Chem. 2022.
PMID: 35649323
A concise synthesis of rhamnan oligosaccharides with alternating α-(1→2)/(1→3)-linkages and repeating α-(1→3)-linkages by iterative α-glycosylation using disaccharide building blocks.
Tanaka H, Hamaya Y, Nishiwaki N, Ishida H.
Tanaka H, et al. Among authors: hamaya y.
Carbohydr Res. 2018 Jan 2;455:23-31. doi: 10.1016/j.carres.2017.11.005. Epub 2017 Nov 14.
Carbohydr Res. 2018.
PMID: 29156420
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A Direct Method for β-Selective Glycosylation with an N-Acetylglucosamine Donor Armed by a 4-O-TBDMS Protecting Group.
Tanaka H, Hamaya Y, Kotsuki H.
Tanaka H, et al. Among authors: hamaya y.
Molecules. 2017 Mar 8;22(3):429. doi: 10.3390/molecules22030429.
Molecules. 2017.
PMID: 28282905
Free PMC article.
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