1,2,3,4-TETRAHYDRO-9-ACRIDINAMINE (321-64-2) 's Synthetic route

Chemiluminescence-promoted oxidation of alkyl enol ethers by NHPI under mild conditions and in the dark

Anderson  Andia, Alexander A.  Woerpel

The hydroperoxidation of alkyl enol ethers using N-hydroxyphthalimide and molecular oxygen occurred in the absence of catalyst, initiator, or light. The reaction proceeds through a radical mechanism that is initiated by N-hydroxyphthalimide-promoted autoxidation of the enol ether substrate. The resulting dioxetane products decompose in a chemiluminescent reaction that allows for photochemical activation of N-hydroxyphthalimide in the absence of other light sources.

PHOTOOXIDATION OF ALKANES AND BENZENE BY POLYVANADATE IN CF3CO2H

Kats, M. M.  Shul'pin, G. B.