Some scientific research about Isoquinolin-3(2H)-one

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Selective, C,C-double bond reduction of alpha,beta-unsaturated carbonyl compounds with cyclohexane using zeolites

Selective ionic hydrogenation of alpha,beta-unsaturated carbonyl compounds with alkanes (cyclohexane and others) was previously known to proceed only in superacidic conditions due to the necessity of dicationic, superelectrophilic activation of the enones. In present paper we disclose that H-form zeolites with acidity well below superacidity, are able however to induce the reduction of alpha,beta-unsaturated carbonyl compounds with cyclohexane in strong analogy to the “parent”, superacid mediated reactions. The probable interpretation of these results in terms of highly electrophilic (superelectrophilic) intermediates on the solid is discussed.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Reference of 7651-81-2. In my other articles, you can also check out more blogs about 7651-81-2

Reference£º
Isoquinoline – Wikipedia,
Isoquinoline | C9H339N – PubChem