209049-06-9

Upstream product

• 53447-88-4 (-)-(1S,2R,4S,6R)-1,2-Cyclohexylidenedioxycyclohexane-4,6-diol 
• 64396-74-3 (1R)-cyclohexanetetrol-(1r,2c,3t,5c) 
• 35949-54-3 (1R,2S,3R,5R)-1,2-O-cyclohexylidene-5-C-(hydroxymethyl)-1,2,3,5-cyclohexanetetrol 
• 53397-93-6 3-O,4-O-cyclohexylidene-(3R,4S,5R)-trihydroxycyclohexan-1-one 
• 74293-60-0 (3aR,7R,7aS)-7-hydroxy-2,2-dimethyltetrahydrobenzo[d][1,3]dioxol-5(6H)-one 

Downstream Products

• 64396-74-3 (1R)-cyclohexanetetrol-(1r,2c,3t,5c) 
• 74538-72-0 C₂₇H₂₄O₇ 

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