73143-47-2

Upstream product

• 73167-60-9 (1S,2R,4R)-2,4-di-O-tosylcyclohexane-1,2,4-triol 
• 73143-45-0 (1S,2R,4R)-1,2-O-cyclohexylidenecyclohexane-1,2,4-triol 
• 73143-44-9 (3R,4S)-3-O,4-O-cyclohexylidene-3,4-dihydroxycyclohexanone 
• 73143-43-8 (4S,5R)-4-O,5-O-cyclohexylidene-4,5-dihydroxycyclohex-2-en-1-one 
• 73209-16-2 (1S,2R,4R)-cyclohexane-1,2,4-triol 

Downstream Products

• 73237-85-1 2,5,6-trideoxystreptamine 
• 73143-48-3 (1S,2S,4S)-2,4-diaminocyclohexanol dihydrochloride salt 
• 63064-89-1 5,6-dideoxyneamine 

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