97119-86-3

Upstream product

• 108-24-7 acetic anhydride 
• 97119-85-2 (1S,2S,3S,6S)-6-((1S,2S,3S,4R,5R)-4-Benzyloxy-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-ylamino)-cyclohex-4-ene-1,2,3-triol 
• 6167-32-4 1,6:3,4-dianhydro-2-O-tosyl-D-galactose 
• 33208-46-7 1,6:3,4-Dianhydro-2-O-benzyl-β-D-galactopyranose 
• 173935-16-5 (+)-conduramine E-4 
• 100-39-0 benzyl bromide 

Downstream Products

• 97119-12-5 1,3,6-Tri-O-acetyl-2-O-benzyl-4-desoxy-4-<1D-(1N,2,4/3)-(2,3,4-tri-O-acetyl-2,3,4-trihydroxy-5-cyclohexen-1-yl)amino>-β-D-glucopyranose 
• 97119-12-5 1,3,6-Tri-O-acetyl-2-O-benzyl-4-desoxy-4-<1D-(1N,2,4/3)-(2,3,4-tri-O-acetyl-2,3,4-trihydroxy-5-cyclohexen-1-yl)amino>-α-D-glucopyranose 

Relevant academic research and scientific papers

Cyclitol Reactions, XII. - Enantioselective Synthesis of the Central Pseudodisaccharide Unit of α-Glycosidase Inhibitors of the Oligostatine Type

A pseudodisaccharide unit of the α-glycosidase inhibitors of the oligostatine type has been synthesized.At first a synthesis of the enantiomeric pure derivative of the branched amino inositol 26 has been developed.A linkage of 26 with the reactive epoxide