89202-34-6

Upstream product

• 130719-07-2 C₂₅H₂₈O₇S 
• 98-88-4 benzoyl chloride 
• 59-23-4 D-Galactose 
• 2782-07-2 D-galactono-1,4-lactone 
• 35556-50-4 2,3,5,6-tetra-O-benzoyl-D-galactono-1,4-lactone 
• 5531-48-6 2,3,5,6-tetra-O-benzoyl-D-galactofuranose 
• 130719-08-3 ethyl 2,3-di-O-benzoyl-1-thio-α-D-galactofuranoside 
• 99773-30-5 5,6-O-isopropylidene-D-galactose diethyl dithioacetal 
• 130719-06-1 ethyl 5,6-O-isopropylidene-1-thio-α-D-galactofuranoside 
• 5463-33-2 D-galactose-diethyl-dithioacetal 
• 89755-45-3 ethyl 2,3,5,6-tetra-O-benzoyl-1-thio-α-D-galactofuranoside 
• 65-85-0 benzoic acid 

Downstream Products

• 502685-22-5 2,5-anhydro-3,4,6,7-tetra-O-benzoyl-D-glycero-L-manno-heptononitrile 
• 108223-95-6 p-nitrophenyl 2,3,5,6-tetra-O-benzoyl-β-D-galactofuranose 
• 108223-94-5 2,3,5,6-tetra-O-benzoyl-β-D-galactofuranose 
• 100645-45-2 (4-nitro)phenyl β-D-galactofuranoside 
• 502685-25-8 2,5-anhydro-4,6,7-tri-O-benzoyl-3-deoxy-D-glycero-L-manno-hept-2-enonitrile 

Relevant academic research and scientific papers

Synthesis of glyceryl glycosides related to A-type prymnesin toxins

A suite of glycosylated glycerol derivatives representing various fragments of the glycosylated ichthyotoxins called prymnesins were chemically synthesised. Glycerol was used to represent a small fragment of the prymnesin backbone, and was glycosylated at

Synthetic biotinylated tetra β(1→5) galactofuranoside for in vitro aspergillosis diagnosis

The synthesis of a tetra β(1→5) galactofuranoside was achieved using a thioglycoside donor with a methyl tert-butyl phenyl thio leaving group. This tetrasaccharide was conjugated to biotin and validated as antigen with the monoclonal antibody used for cli

Non-natural aldofuranosides as substrates of a β-glucosidase

Based on glycosidase inhibitory activities of some known 1,4-iminoalditols, four aldofuranosides, (4-nitro)phenyl β-d-glucofuranoside, -β-d-galactofuranoside, -α-l-idofuranoside and -α-l- altrofuranoside, were identified as possible substrates of glucosid

A convenient iodonium-ion-assisted synthesis of an immunologically active tetrameric β(1->5)-linked D-galactofuranoside from the extracellular polysaccharide of Aspergillus and Penicillium species

The non-terminal glycosyl donor, ethyl 2,3-di-O-benzoyl-5-O-(chloroacetyl)-6-O-pivaloyl-1-thio-α-D-galactofuranoside, could be used, with the promotor N-iodosuccinimide and catalytic trifluoromethanesulfonic acid, for the preparation of β-D-galf-(1->5)-β-

PROTON AND C-13 NUCLEAR MAGNETIC RESONANCE SPECTRA OF SOME BENZOYLATED ALDOHEXOSES

Chemical shifts and coupling constants of 1H-n.m.r. spectra of the perbenzoates of α-D-glucopyranose (1), β-D-glucopyranose (2), α-D-galactopyranose (3), α-D-mannopyranose (4), β-D-mannopyranose (5), and α-D-galactofuranose (6) are reported.The 13C-n.m.r.