Halogenation of N-Substituted p-Quinonimines and p-Quinone Oxime Esters: I. Chlorination and Bromination of 4-Aroyloxyimino- and Arylsulfonyloxyimino-2,5-cyclohexadienones

Autor: Avdeenko, A., Shishkina, S., Shishkin, O., Glinyanaya, N., Konovalova, S., Goncharova, S.
Zdroj: Russian Journal of Organic Chemistry; May 2002, Vol. 38 Issue: 5 p683-691, 9p
Abstrakt: Chlorine and bromine addition to 4-aroyloxyimino- and 4-arylsulfonyloxymino-3-methyl-2,5-cyclohexadienones initially occurs at the C5ÍC6double bond. The second chlorine molecule adds at both C2ÍCand C5ÍC6double bonds. The chlorination of 2,5-dialkyl-substituted 4-aroyloxyimino- and 4-arylsulfonyloxymino-2,5-cyclohexadienones involves either of the CÍC bonds in the quinoid ring.
Databáze: Supplemental Index
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