77117-51-2

Upstream product

• 67-56-1 methanol 
• 50266-00-7 cis,cis,cis,cis,cis-1,2,3,4,5,6-cyclohexanehexacarboxylicacid 
• 186581-53-3 diazomethane 
• 56745-93-8 2,3,5,6-exo-bicyclo<2.2.2>-7-octene-2,3,5,6-tetracarboxylic acid tetramethyl ester 

Downstream Products

• 83861-33-0 myo-cyclohexane-1,2,3,4,5,6-hexacarboxylic acid hexamethyl ester 
• 83238-59-9 muco-cyclohexane-1,2,3,4,5,6-hexacarboxylic acid hexamethyl ester 
• 94054-02-1 scyllo-1,3,5/2,4,6-hexakis(methoxycarbonyl)cyclohexane 
• 94054-01-0 chiro-1,2,4/3,5,6-hexakis(methoxycarbonyl)cyclohexane 

Relevant academic research and scientific papers

Ring Reversal of cis-Cyclohexane-1,2,3,4,5,6-hexacarboxylic Acid and its Hexamethyl Ester

cis-Cyclohexane-1,2,3,4,5,6-hexacarboxylic acid and its hexamethyl ester have been synthesized and shown, by n.m.r. to exist in solution at room temperature as an equilibrium of slowly exchanging chair conformations.From complete line shape analysis of th

STEREOCHEMISTRY OF SUBSTITUTED BICYCLOOCTENES

The epimerization of the methyl ester of 2,3,5,6-endo-bicyclo-7-octenetetracarboxylic acid produces three stereoisomers with one or two substituents in the exo position.Their structure was determined by 13C- and 1H-NMR spectroscopy and reactivity s