73167-60-9

Upstream product

• 73209-16-2 (1S,2R,4R)-cyclohexane-1,2,4-triol 
• 98-59-9 p-toluenesulfonyl chloride 
• 73143-45-0 (1S,2R,4R)-1,2-O-cyclohexylidenecyclohexane-1,2,4-triol 
• 73143-43-8 (4S,5R)-4-O,5-O-cyclohexylidene-4,5-dihydroxycyclohex-2-en-1-one 
• 73143-44-9 (3R,4S)-3-O,4-O-cyclohexylidene-3,4-dihydroxycyclohexanone 
• 73180-35-5 Toluene-4-sulfonic acid (1R,3R,4S)-3,4-dihydroxy-cyclohexyl ester 

Downstream Products

• 63064-89-1 5,6-dideoxyneamine 
• 73143-50-7 Acetic acid (2S,3R,5S,6R)-5-acetoxy-2-[(1S,2R,4R)-2,4-bis-(toluene-4-sulfonyloxy)-cyclohexyloxy]-6-(toluene-4-sulfonyloxymethyl)-tetrahydro-pyran-3-yl ester 
• 73237-85-1 2,5,6-trideoxystreptamine 
• 73143-48-3 (1S,2S,4S)-2,4-diaminocyclohexanol dihydrochloride salt 
• 73143-47-2 (1S,2S,4S)-2,4-diazidocyclohexanol 

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