57357-87-6

Upstream product

• 61431-01-4 (1R,2R,4S,6R)-6-chloro-2,4-di-O-tosylcyclohexane-1,2,4-triol 
• 53398-05-3 (1S,2R,3R,5S)-1,2-anhydro-5-O-tosylcyclohexane-1,2,3,5-tetrol 
• 98-59-9 p-toluenesulfonyl chloride 
• 53397-95-8 C₂₆H₃₂O₈S₂ 
• 53397-93-6 3-O,4-O-cyclohexylidene-(3R,4S,5R)-trihydroxycyclohexan-1-one 
• 35949-54-3 (1R,2S,3R,5R)-1,2-O-cyclohexylidene-5-C-(hydroxymethyl)-1,2,3,5-cyclohexanetetrol 
• 57357-88-7 C₂₀H₂₄O₈S₂ 

Downstream Products

• 74538-63-9 (1r,2S,4r,6R)-2,4,6-triazidocyclohexanol 
• 57357-88-7 (1R,2S,3R,5R)-1,5-di-O-tosylcyclohexane-1,2,3,5-tetrol 
• 57378-79-7 (1R,2R,3S,5S)-3,5-diazidocyclohexane-1,2-diol 
• 74538-65-1 (1r,2S,4r,6R)-2,4,6-triaminocyclohexanol trihydrochloride salt 
• 53398-02-0 (1R,2R,3S,5R)-3,5-diaminocyclohexane-1,2-diol dihydrochloride salt 
• 69240-16-0 (1R,2S,3R,5R)-3-O-tert-butyldimethylsilyl-1,5-di-O-tosylcyclohexane-1,2,3,5-tetrol 
• 69240-05-7 (1R,2S,3R,5R)-2-O-benzoyl-1,5-di-O-tosylcyclohexane-1,2,3,5-tetrol 

Relevant academic research and scientific papers

SYNTHESIS OF AMINOCYCLITOLS FROM L-QUINIC ACID

A variety of 1,3-diamino and 1,4-diaminocyclitols, monoaminocyclitols, and triaminocyclohexanol have been synthesized starting with the chiral ketone intermediate 2, derived from L-quinic acid.Reduction of 2 with lithium borohydride afforded two epimeric