Issue 4, 1998

On the nature of the intermediate in the Lewis acid- promoted synthesis of dihydroisoquinolines from nitriles and β-phenylethyl chloride

Abstract

In addition to Lewis acidity, the ability to co-ordinate both reactants is a prerequisite for catalyst activity in the cyclisation reaction of β-phenylethyl chloride and alkyl- or aryl nitriles to dihydroisoquinolines.

Article information

Article type
Paper

Mendeleev Commun., 1998,8, 153-154

On the nature of the intermediate in the Lewis acid- promoted synthesis of dihydroisoquinolines from nitriles and β-phenylethyl chloride

E. A. Mistryukov and O. N. Sorokina, Mendeleev Commun., 1998, 8, 153 DOI: 10.1070/MC1998v008n04ABEH000955

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