900792-05-4

Upstream product

• 40635-67-4 acetoxyisobutyryl bromide 
• 320410-60-4 (1R,2R,3S,4S)-5-iodocyclohex-5-ene-1,2,3,4-tetraol 
• 165611-18-7 (3aS,4R,5R,7aS)-7-iodo-2,2-dimethyl-3a,4,5,7a-tetrahydro-1,3-benzodioxole-4,5-diol 
• 154784-39-1 (3aS,7aS)-4-iodo-2,2-dimethyl-3a,7a-dihydro-1,3-benzodioxole 
• 138769-92-3 cis-(1S,2S)-1,2-dihydroxy-3-iodocyclohexa-3,5-diene 

Downstream Products

• 858037-17-9 methyl (1R,2S,3R,4R,5S)-2,3,4,5-tetra(acetyloxy)cyclohexane-1-carboxylate 
• 856890-19-2 methyl (3S,4R,5R,6S)-3,4,5,6-tetra(acetyloxy)-1-cyclohexene-1-carboxylate 
• 86117-81-9 (1S,2R,3R,4S,5S)-5-(hydroxymethyl)cyclohexane-1,2,3,4-tetraol 
• 320410-71-7 (1R,2R)-4-iodo-3,5-cyclohexadiene-1,2-diol 
• 856890-18-1 (1R,2S,5R,6S)-2,5,6-tri(acetyloxy)-4-iodo-3-cyclohexenyl acetate 

Relevant academic research and scientific papers

Chemoenzymatic synthesis of the trans-dihydrodiol isomers of monosubstituted benzenes via anti-benzene dioxides

Enantiopure cis-2,3-dihydrodiols, available from dioxygenase-catalysed cis-dihydroxylation of monosubstituted benzene substrates, have been used as synthetic precursors of the corresponding trans-3,4-dihydrodiols. The six-step chemoenzymatic route from ci

Chemoenzymatic synthesis of carbasugars from iodobenzene

The versatile enantiopure cis-dihydrodiol metabolite 1, formed by bacterial metabolism of iodobenzene, has been used for the synthesis of the pyranose carbasugars (pseudosugars) carba-β-D-altropyranose 2, carba-α-L- galactopyranose 3, carba-β-D-idopyranos

Enantiopure arene dioxides: Chemoenzymatic synthesis and application in the production of trans-3,4-dihydrodiols

Enantiopure syn- and anti-arene dioxides are synthesised from cis-dihydrodiol metabolites; anti-benzene dioxides are reduced to enantiopure trans-3,4-dihydrodiols while synbenzene dioxides racemise thermally via 1,4-dioxocins.