69895-14-3

Upstream product

• 34234-44-1 methyl 2,3,4-tri-O-benzoylglucopyranoside 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 572-09-8 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl bromide 
• 98-88-4 benzoyl chloride 
• 1079152-12-7 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranosyl N-phenyl trifluoroacetimidate 
• 13350-45-3 methyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside 
• 1242659-80-8 p-octyloxyphenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside 
• 20231-39-4 methyl 2,3,4-tri-O-benzoyl-6-O-triphenylmethyl-α-D-glucopyranoside 
• 259669-32-4 Acetic acid (2S,3aR,5R,6R,7S,7aR)-6-acetoxy-5-acetoxymethyl-2-methyl-2-((2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-[1,3]dioxolo[4,5-b]pyran-7-yl ester 
• 97-30-3 methyl-alpha-D-glucopyranoside 
• 311806-04-9 C₄₂H₄₄O₁₈ 

Downstream Products

• 4159-55-1 methyl 6-O-(β-D-glucopyranosyl)-α-D-glucopyranoside 
• 311806-05-0 methyl β-D-glucopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-glucopyranoside 
• 311806-06-1 C₆₉H₆₆O₂₆ 

Relevant academic research and scientific papers

Glycosylation reaction of thioglycosides by using hypervalent iodine(III) reagent as an excellent promoter

Thioglycosides are available donors in glycosylation due to the stability of the anomeric C-S bond under general reaction conditions of protection and deprotection, and offer orthogonality in their activation. We report now that the hypervalent iodine eff

Enviromentally-benign glycosylation reaction using odorless thio-glycosides and hypervalent iodine(III) reagent

We discovered that the hypervalent iodine(III) reagent could mediate the glycosylation reaction by activating the thio-glycoside donors which were prepared from glycosyl 1-O-acetate and odorless p-octyloxybenzenethiol. By using this method, trisaccharides

Catalytic glycosylation with glycosyl thioimidate donors

A new class of glycosyl thioimidates, glycosyl N-phenyl- trifluorothioacetimidates, were prepared from the readily available glycosyl thiols in excellent yields. These imidates exhibited very good donor properties under the action of catalytic amounts of BF3·Et2O, and the corresponding glycosidation products were formed in very good to excellent yields. Thus, the first catalytic glycosylations with glycosyl thioimidate donors were achieved. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

Regio- and stereoselective synthesis of 1→6 linked manno-, gluco-, and galactopyranose Di-, Tri-, and tetrasaccharides via orthoester intermediates

1→6 linked manno-, gluco-, and galactopyranose di-, tri-, and tetrasaccharides with 1,2-trans glycosidic linkages were concisely and effectively synthesized using peracetylated glycosyl bromides as the donors and unprotected or partially protected glycopy