Add time:09/28/2019 Source:sciencedirect.com
The oxidation of N-[1-Methyl-2:3-dihydroxy-cyclopenten(2)-ylidene(4)] piperidinium betaine(I) was investigated using electrochemical methods. The betaine was observed to be oxidised in an irreversible two-electron process to give fragmentation products. The major product resulted from the attack of piperidine on the enamine intermediate which is obtained through the two-electron oxidation of (I).
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