180475-16-5

Upstream product

• 62-53-3 aniline 
• 1625-83-8 9,10-dihydro-9,10-etheno-11,12-anthracenedicarboxylic acid anhydride 
• 1625-81-6 9,10-dihydro-9,10-ethenoanthracene-11,12-dicarboxylic acid 
• 1625-82-7 Dimethyl 9,10-dihydro-9,10-ethenoanthracene-11,12-dicarboxylate 
• 120-12-7 anthracene 

Relevant academic research and scientific papers

Synthesis of the formal Diels-Alder adducts of N-substituted dehydromaleimides and anthracene

A new class of roof-shaped dibenzobarrelenemaleimide derivatives was prepared by the condensation of a bridged maleic anhydride with amines. A para-substituted bifunctional derivative was proven to be a 1:2 complex with acetone by an X-ray crystallographic study.

Electro-organic reactions. Part 46. Diels-Alder trapping of o-quinodimethane generated by redox-mediated cathodic reduction of α,α′-dibromo-o-xylene in the presence of hindered dienophiles

Hindered, electron-deficient alkenes 5-11 have been prepared, including analogues of maleic anhydride, N-phenylmaleimide and benzoquinone. Cyclic voltammetry showed that most of these compounds can undergo reduction to form relatively persistent radical-a