97119-82-9

Upstream product

• 33208-46-7 1,6:3,4-Dianhydro-2-O-benzyl-β-D-galactopyranose 
• 108-91-8 cyclohexylamine 
• 100-39-0 benzyl bromide 
• 6167-32-4 1,6:3,4-dianhydro-2-O-tosyl-D-galactose 

Downstream Products

• 190791-71-0 (1S,2R,6S,7R,8R)-7-Benzyloxy-3-cyclohexyl-5,9,11-trioxa-3-aza-tricyclo[6.2.1.0^2,6]undecan-4-one 
• 97119-84-1 1,3,6-Tri-O-acetyl-2-O-benzyl-4-(cyclohexylamino)-4-desoxy-α-D-glucopyranose 
• 97119-84-1 1,3,6-Tri-O-acetyl-2-O-benzyl-4-(cyclohexylamino)-4-desoxy-β-D-glucopyranose 
• 190791-74-3 Acetic acid (1S,2R,6S,7R,8R)-3-cyclohexyl-4-oxo-5,9,11-trioxa-3-aza-tricyclo[6.2.1.0^2,6]undec-7-yl ester 
• 97119-83-0 3-O-Acetyl-1,6-anhydro-2-O-benzyl-4-(cyclohexylamino)-4-desoxy-β-D-glucopyranose 

Relevant academic research and scientific papers

β-acarbose. IV. Model studies on the alkylation of cyclohexylamine with a carbohydrate epoxide

1,6:3,4-Dianhydro-2-O-benzyl-β-D-galactose has been treated with cyclohexylamine to give an amino alcohol, convertible into 2,3-di-O-acetyl-1,6-anhydro-4-cyclohexylamino-4-deoxy-β-D-glucose by reduction and acetylation. The anhydro bridge of this diacetat

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