53691-39-7

Upstream product

• 3867-86-5 Brigl's anhydride 
• 100-51-6 benzyl alcohol 
• 1104490-22-3 benzyl 3,4,6-tri-O-acetyl-2-O-iodoacetyl-β-D-glucopyranoside 
• 4451-37-0 3,4,6-tri-O-acetyl-β-D-glucopyranosyl chloride 
• 74808-10-9 2,3,4,6-tetra-O-acetyl-d-glucopyranosyl trichloroacetimidate 
• 171233-72-0 Acetic acid (3aR,5R,6R,7S,7aR)-6-acetoxy-5-acetoxymethyl-2-oxo-tetrahydro-2λ⁴-[1,3,2]dioxathiolo[4,5-b]pyran-7-yl ester 

Downstream Products

• 52591-34-1 benzyl-[O³,O⁴,O⁶-triacetyl-O²-(toluene-4-sulfonyl)-β-D-glucopyranoside] 

Relevant academic research and scientific papers

Facile synthesis of 2-0-lodoacetyl protected glycosyl iodides: Useful precursors of 1→2-linked 1,2-trans-glycosides

(Chemical Equation Presented) The preparation and utilization of novel iodide glycosyl donors, 2-0-iodoacetyl-glycopyranosyl iodides, is described. The mechanism for the reaction of iodine with carbohydrate cyclic ketene acetal was investigated through lo

Glycosylation in ionic liquids

Glycosyl trichloroacetimidates react smoothly in the presence of trimethylsilyl trifluoromethanesulfonate as a catalyst with a variety of alcohols and monosaccharides in [bmim]PF6 (1-butyl-3-methylimidazolium hexafluorophosphate) as a solvent to afford the corresponding glycosides or disaccharides.

Stereoselective, Lewis acid-catalyzed glycosylation of alcohols by glucose 1,2-cyclic sulfites

α-D-Glucopyranose-1,2-cyclic sulfites (1a-c) have been prepared by reaction of a suitably protected glucose residue and thionyl diimidazole. Reaction of these compounds with alcohols in the presence of Yb(OTf)3 or Ho(OTf)3 stereosele