105453-64-3

Usage

InChI:InChI=1/C22H16O2/c23-21-10-9-17-18(22(21)24)8-7-15-11-19-14(12-20(15)17)6-5-13-3-1-2-4-16(13)19/h1-12,21-24H

Upstream product

• 72591-27-6 3,4-dibromodibenzanthracene-3,4-quinone 
• 66267-19-4 trans-3,4-dihydroxy-3,4-dihydrodibenzanthracene 
• 72378-85-9 C₃₆H₂₅BrO₄ 
• 72378-81-5 trans-3,4-bis(benzoyloxy)-3,4-dihydrodibenzanthracene 
• 72378-84-8 trans-3,4-bis(benzoyloxy)-1,2,3,4-tetrahydrodibenzanthracene 
• 70644-35-8 dibenzanthracene-3,4-quinone 
• 66267-17-2 trans-3,4-diacetoxy-3,4-dihydrodibenzanthracene 

Downstream Products

• 161906-53-2 (-)-(1S,2R,3R,4S)-3,4-dihydroxy-1,2-epoxy-1,2,3,4-tetrahydrodibenz[a,h]anthracene 

Relevant academic research and scientific papers

Synthesis, absolute configuration, and bacterial mutagenicity of the 8 stereoisomeric vicinal diol epoxides at the terminal benzo ring of carcinogenic dibenz[ a,h ]anthracene

The synthesis of the 8 possible stereoisomeric diol epoxides (DEs) at the terminal benzo ring of carcinogenic dibenz[a,h]anthracene (DBA) is reported. trans-3,4-Dihydroxy-3,4-dihydro-DBA (1) afforded the 4 bay region DEs: the enantiomeric pairs of the ant

Reduction of ortho-Quinones to Dihydrodiols

1,2-Naphthaquinone, 5-bromo-1,2-naphthaquinone and dibenzanthracene-3,4-quinone in the form of dibromo-intermediates were reduced to a mixture of cis- and trans-diols by the action of sodium borohydride in ethanol.An alternative synthesis of trans-3,4-dihydroxy-3,4-dihydrodibenzanthracene is also reported.