64353-73-7

Upstream product

• 64353-72-6 C₁₉H₂₃ClO₄ 

Downstream Products

• 74538-77-5 C₂₇H₂₅ClO₇S 
• 74538-78-6 (1R,2S,3R,5R)-2-O-benzoyl-3-O-benzyl-5-chloro-1-O-tosylcyclohexane-1,2,3-triol 
• 74538-79-7 (1R,2S,3R)-2,3-di-O-benzoyl-1-O-tosylcyclohexane-1,2,3-triol 
• 74538-80-0 (1R,2S,3R)-2-O-benzoyl-3-O-benzyl-1-O-tosylcyclohexane-1,2,3-triol 
• 74538-62-8 (1R,2S,3R,5R)-3-O-benzyl-5-chloro-1-O-tosylcyclohexane-1,2,3-triol 
• 74538-81-1 Toluene-4-sulfonic acid (1R,2S,3R)-3-benzyloxy-2-hydroxy-cyclohexyl ester 
• 53398-02-0 (1R,2R,3S,5R)-3,5-diaminocyclohexane-1,2-diol dihydrochloride salt 
• 64353-74-8 (1R,2S,3R,5R)-5-chloro-1-tosylcyclohexane-1,2,3-triol 
• 74644-03-4 (1R,2R,3S)-3-aminocyclohexane-1,2-diol hydrobromide salt 
• 57378-79-7 (1R,2R,3S,5S)-3,5-diazidocyclohexane-1,2-diol 
• 64493-23-8 (1R,2S,3R,5R)-3-O-benzoyl-5-chloro-1-O-tosylcyclohexane-1,2,3-triol 

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