108032-89-9

Upstream product

• 613-90-1 benzoyl cyanide 
• 107960-18-9 (2S,3R,4S,5S)-2,3,4-Tris-benzyloxy-5-ethylsulfanyl-5-hydroxymethyl-cyclohexanol 
• 606930-14-7 (2S,3R,4S)-2,3,4-tris-benzyloxy-5-hydroxycyclohexan-1-one 
• 107960-16-7 1L-(1S,2,4/1C,3)-5-O-Acetyl-2,3,4-tri-O-benzyl-1-C-(ethylthio)-2,3,4,5-tetrahydroxy-1-cyclohexancarbonitril 

Downstream Products

• 110372-69-5 2D-(2,4,5S/3,5C)-5-C-(Benzoyloxy)methyl-2,3,4-tri-O-benzyl-5-C-(ethylthio)-2,3,4-trihydroxy-1-cyclohexanon 
• 110372-71-9 2D-(2,4/3)-5-C-(Benzoyloxy)methyl-2,3,4-tri-O-benzyl-2,3,4-trihydroxy-5-cyclohexen-1-on 
• 75348-20-8 1L-(1,3/2,4)-7-O-Benzoyl-2,3,4-tri-O-benzyl-5-C-hydroxymethyl-tetrahydroxy-5-cyclohexen 
• 110454-00-7 1D-(1,2,4/3)-5-C-(Benzoyloxy)methyl-2,3,4-tri-O-benzyl-5-cyclohexen-1,2,3,4-tetrol 
• 107960-21-4 Benzoic acid (3S,4S,5S,6R)-4,5,6-tris-benzyloxy-3-(toluene-4-sulfonylamino)-cyclohex-1-enylmethyl ester 

Relevant academic research and scientific papers

α-Glucosidase Inhibitors, 5.- Investigations towards a Synthesis of C1-Branched Cyclitols from D-Glucose

The glucose derivatives 1 and 2 were transformed by Ferrier rearrangement as one of the reaction steps into the cyclitol derivatives 3a,b and 4a,b, respectively.The attachment of a functional C1-side chain at the carbonyl group was tested with