110453-99-1

Upstream product

• 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 
• 107960-17-8 1L-(1S,2,4/1C,3)-2,3,4-Tri-O-benzyl-1-(ethylthio)-2,3,4,5-tetrahydroxy-1-cyclohexancarbaldehyd 

Downstream Products

• 108032-89-9 1D-(1,2,4,5S/3,5C)-5-C-(Benzoyloxy)methyl-2,3,4-tri-O-benzyl-5-C-(ethylthio)-1,2,3,4-cyclohexantetrol 
• 107960-19-0 Benzoic acid (1S,2S,3R,4S,5R)-2,3,4-tris-benzyloxy-1-ethylsulfanyl-5-hydroxy-cyclohexylmethyl ester 
• 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 
• 75348-20-8 1L-(1,3/2,4)-7-O-Benzoyl-2,3,4-tri-O-benzyl-5-C-hydroxymethyl-tetrahydroxy-5-cyclohexen 
• 105017-77-4 1D-(1,2,4/3)-2,3,4-Tri-O-benzyl-5-C-(hydroxymethyl)-5-cyclohexen-1,2,3,4-tetrol 
• 75348-19-5 1L-(1,2/2,4)-2,3,4-Tri-O-benzyl-5-C-(hydroxymethyl)-5-cyclohexen-1,2,3,4-tetrol 
• 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 
• 110372-68-4 2D-(2,4,5S/3,5C)-2,3,4-Tri-O-benzyl-5-C-<(tert-butyldimethylsilyloxy)methyl>-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 
• 110391-09-8 2D-(2,3,5S/3,5C)-2,3,4-Tri-O-benzyl-5-C-<(benzyloxy)methyl>-5-C-(ethylthio)-2,3,4-trihydroxy-1-cyclohexanon 
• 110372-64-0 1D-(1,2,4S/2,4C)-1,2,3-Tri-O-benzyl-4-C-<(tert-butyldimethylsilyloxy)methyl>-4-C-(ethylthio)-5-cyclohexen-1,2,3-triol 
• 110372-70-8 1D-(1,2,4/3)-2,3,4-Tri-O-benzyl-5-C-<(tert-butyldimethylsilyloxy)methyl>-5-cyclohexen-1,2,3,4-tetrol 
• 110372-72-0 2D-(2,4/3)-2,3,4-Tri-O-benzyl-5-C-(hydroxymethyl)-2,3,4-trihydroxy-5-cyclohexen-1-on 
• 110391-10-1 (4R,5S,6R)-4,5,6-tris(benzyloxy)-3-((benzyloxy)methyl)-2-cyclohexen-1-one 

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