Protection-free Synthesis of Alkyl Glycosides under Hydrogenolytic Conditions

A dimethoxytriazine type glycosyl donor enables a facile chemo-enzymatic route toward α-linked N-acetylglucosaminyl-galactose disaccharide unit from gastric mucin

(2012) Masato Noguchi et al.   CHEMICAL COMMUNICATIONS

4,6-Dimethoxy-1,3,5-triazin-2-yl β-d-glycosaminides: Novel Substrates for Transglycosylation Reaction Catalyzed by Exo-β-d-glucosaminidase fromAmycolatopsis orientalis

(2012) Tomonari Tanaka et al.   JOURNAL OF CARBOHYDRATE CHEMISTRY

Use ofN,O-Dimethylhydroxylamine As an Anomeric Protecting Group in Carbohydrate Synthesis

(2011) Somnath Dasgupta et al.   JOURNAL OF ORGANIC CHEMISTRY

4,6-Dimethoxy-1,3,5-triazine oligoxyloglucans: Novel one-step preparable substrates for studying action of endo-β-1,4-glucanase III from Trichoderma reesei

(2010) Atsushi Kobayashi et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

Novel dialkoxytriazine-type glycosyl donors for cellulase-catalysed lactosylation

(2010) Tomonari Tanaka et al.   ORGANIC & BIOMOLECULAR CHEMISTRY

A novel glycosyl donor for chemo-enzymatic oligosaccharide synthesis: 4,6-dimethoxy-1,3,5-triazin-2-yl glycoside

(2008) Tomonari Tanaka et al.   CHEMICAL COMMUNICATIONS

Protecting Group Free Glycosidations Usingp-Toluenesulfonohydrazide Donors

(2008) Anna V. Gudmundsdottir et al.   ORGANIC LETTERS