129706-51-0

Upstream product

• 28642-64-0 methyl 2-O-benzoyl-4,6-di-O-benzylidene-α-D-glucopyranoside 
• 13242-53-0 acetobromomannose 
• 121238-27-5 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl trichloroimidate 

Downstream Products

• 129658-98-6 methyl 2-O-benzoyl-4,6-O-benzylidene-3-O-(α-D-mannopyranosyl)-α-D-glucopyranoside 
• 129659-00-3 methyl 4,6-O-benzylidene-3-O-(2,3:4,6-di-O-isopropylidene-α-D-mannopyranosyl)-α-D-glucopyranoside 
• 129658-99-7 methyl 2-O-benzoyl-4,6-O-benzylidene-3-O-(2,3:4,6-di-O-isopropylidene-α-D-mannopyranosyl)-α-D-glucopyranoside 

Relevant academic research and scientific papers

Iron(iii) chloride modulated selective 1,2-trans glycosylation based on glycosyl trichloroacetimidate donors and its application in orthogonal glycosylation

The development of a new glycosylation method for efficient stereoselective synthesis of β-gluco- and galactosides from their corresponding armed trichloroacetimidate donors mediated by 10 mole% of FeCl3 has been focused. FeCl3 has a

Anomalous Zemplen deacylation reactions of 2-O-acyl-3-O-alkyl or -3-O-glycosyl derivatives of D-galactose and D-glucose: synthesis of O-alpha-D-mannopyranosyl-(1----4)-O-alpha-L-rhamnopyranosyl-(1----3)-D- galactose and an intermediate for the preparation of 2-O-glycosyl-3-O-(alpha-D-mannopyranosyl)-D-glucoses.

Treatment of 2-O-benzoyl (1) and 2-O-acetyl (5) derivatives of benzyl 4,6-benzylidene-3-O-(2,3,4-tri-O-acetyl-alpha-L-rhamnopyranosyl)-beta-D- galactopyranoside under Zemplen conditions (catalytic amount of sodium methoxide in methanol) gave partially deacylated disaccharides in which the 2-O-acyl groups were retained. Likewise, a similar result was obtained with the beta-L-rhamnopyranosyl analogue (3) of 1. This anomalous reaction was used in a synthesis of the title trisaccharide (17) and of methyl 4,6-O-benzylidene-3-O-(2,3:4,6-di-O-isopropylidene-alpha-D-mannopyranosy l)- alpha-D-glucopyranoside, an intermediate for the synthesis of 2-O-glycosyl-3-O-(alpha-D-mannopyranosyl)-D-glucoses.