
Abstract The reaction of cyclohexanones with copper(II) chloride gave polychlorinated cyclohexanediones directly in fairly good yields. With methylcyclohexanones, in general the type of product depends on the number of methylene groups between the carbonyl group and the methyl-substituted carbon in the starting material. A possible mechanism for the reaction is discussed.
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 16 | |
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| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
