671199-44-3

Upstream product

• 89533-81-3 4,5,6-trihydroxycyclohex-2-ene-1-one 
• 1190844-34-8 (4S,5R,6S)-4,5,6-trihydroxy-2-cyclohexene-1-one 
• 671199-46-5 (4R,5S,6R)-4,5,6-tris(benzyloxy)cyclohex-2-en-1-one 

Downstream Products

• 18424-51-6 (1R)-cyclohexane-1r,2c,3c,4t-tetraol 
• 2630-65-1 (1α,2β,3α)-1,2,3-cyclohexanetriol 
• 18422-07-6 (1R)-1r,2t,3c,4t-tetrakis-benzoyloxy-cyclohexane 
• 18424-50-5 (3R)-3r,4t-dihydroxy-cyclohexane-1,2-dione-bis-phenylhydrazone 
• 78147-99-6 (-)-1L-Cyclohexane-1,3/2,4-tetrol 
• 129938-05-2 (1S,2S,3S,4R)-cyclohexane-1,2,3,4-tetrol 
• 18422-07-6 (1R)-1r,2c,3c,4t-tetrakis-benzoyloxy-cyclohexane 

Relevant academic research and scientific papers

CATECHOL MANUFACTURING METHOD

Provided is a method for producing catechol in a one-pot by reacting (4S,5R,6S)-4,5,6-trihydroxy-2-cyclohexene-1-one under hydrogen-reducing conditions while heating.

Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohexanone from D-glucose

We have described the synthesis of (+)-(2R,3S,4R)-2,3,4- trihydroxycyclohexanone by the reduction of a keto-conduritol derivative, the latter being prepared in five steps from (-)-(2S,3R,4S,5S)-2,3,4-tribenzyloxy-5- hydroxycyclohexanone, which is in turn

Synthesis of polyhydroxylated cyclohexenyl sulfides and sulfoxides. Evaluation of their inhibitory activity on α- and β-D-glucosidases

Racemic polyhydroxylated sulfides and sulfoxides have been prepared as potential transition-state analogs of the glucoside hydrolysis reaction, through a reaction sequence involving transformations of a ketone group into thioacetal, followed by partial ox