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This article is cited in 3 scientific papers (total in 3 papers)
On the nature of the intermediate in the Lewis acid-promoted synthesis of dihydroisoquinolines from nitriles and β-phenylethyl chloride
E. A. Mistryukov, O. N. Sorokina
N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract:
In addition to Lewis acidity, the ability to co-ordinate both reactants is a prerequisite for catalyst activity in the cyclisation reaction of b-phenylethyl chloride and alkyl β-or aryl nitriles to dihydroisoquinolines.
Citation:
E. A. Mistryukov, O. N. Sorokina, “On the nature of the intermediate in the Lewis acid-promoted synthesis of dihydroisoquinolines from nitriles and β-phenylethyl chloride”, Mendeleev Commun., 8:4 (1998), 153–154
Linking options:
https://www.mathnet.ru/eng/mendc4703 https://www.mathnet.ru/eng/mendc/v8/i4/p153
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