Electrochemical study of the sequence of reductive dehalogenation of 2-bromo-5-dibromomethyl-4-dichloromethyl-4-methylcyclohexa-2,5-dien-1-on e and its analogsстатья
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Дата последнего поиска статьи во внешних источниках: 18 июля 2013 г.
Аннотация:The electrochemical behavior of a series of halo.-en-containing cyclohexa-2,5-dien-1-ones at the glassy-carbon electrode in DMF was Studied. The reductive dehalogenation of 2-bromo-5-dibromomethyl-4-dichloromethyl-4-methylcyclohexa-2,5-dien-1-on e first results in the elimination of the carbonylallylic bromine atoms, then the carbonylic bromine atom is eliminated, and finally, the neopentylic chlorine atoms are eliminated.