26931-79-3

Upstream product

• 1488-25-1 benzene oxide 
• 64287-99-6 trans-1,2-Diacetoxy-4,5-dibromcyclohexan 
• 39078-08-5 rac-(3R,4R,5R,6R)-3,4:5,6-diepoxycyclohex-1-ene 
• 64288-00-2 trans-cyclohexa-3,5-diene-1,2-diyl diacetate 
• 36635-14-0 (+/-)-3c,4t,5t,6c-tetrachloro-cyclohexane-1r,2t-diol 
• 121073-05-0 Acetic acid (1R,6R)-6-hydroxy-cyclohexa-2,4-dienyl ester 

Downstream Products

• 4381-96-8 (+/-)-tetraacetylconduritol C 
• 20097-40-9 hexa-O-acetyl-neo-inositol 
• 4381-96-8 (+/-)-tetra-O-acetylconduritol F 
• 1254-38-2 chiro-inositol hexaacetate 
• 108-95-2 phenol 
• 526-87-4 (+/-)-Conduritol B 
• 526-87-4 conduritol A 
• 129662-32-4 trans-1,2-Di-O-(2-methoxyethoxymethyl)cyclohexa-3,5-diene-1,2-diol 
• 64330-65-0 cis,cis-2,4-hexadienedial 
• 64288-00-2 trans-cyclohexa-3,5-diene-1,2-diyl diacetate 
• 583-63-1 ortoquinone 
• 70134-77-9 (-)-(1R,2S,3R,6S)-7-oxabicyclo<4.1.0>hept-4-ene-2,3-diol 
• 35949-67-8 (1R,2S,3R,4R,5R,6S)-3,6-Bis-benzyloxy-cyclohexane-1,2,4,5-tetraol 
• 70134-77-9 (1R,2R,3S,6S)-7-Oxa-bicyclo[4.1.0]hept-4-ene-2,3-diol 

Relevant academic research and scientific papers

Concerning the reaction of anti-benzene dioxide with various nucleophiles

trans-3,4:5,6-Diepoxycyclohex-1-ene (anti-benzene dioxide) (5) was brought into reaction with several S, O, and C nucleophiles. S and O nucleophiles gave the bis-adducts stemming from independent reaction of the two epoxy functions. C nucleophiles, on the

Resolution of trans-1,2-Dihydroxy-1,2-dihydrobenzene for the Preparation of Optically Pure Benzene Diol Epoxides. Preparation of Bromo- and Chlorobenzene Diol Epoxides

The resolution of (+/-)-trans-1,2-dihydroxy-1,2-dihydrobenzene has been accomplished by esterase-catalysed hydrolysis of diacetate (+/-)-5.Peracid epoxidation of (+)-2 and (-)-2 gave diol epoxides (+)-3 and (-)-3, respectively.The synthesis of d