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.
Document Type:
Article
Language: English
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
This publication is cited in the following 3 articles:
Saad S. Elmorsy, Ahmed M. Sheta, Mohammad M. A. Mashaly, Samy B. Said, “Tetrachlorosilane and zinc chloride as a binary reagent for the preparation of 2-amino-6-chloropyridine-3,5-dicarbonitrile derivatives”, Chem Heterocycl Comp, 53:5 (2017), 540
Mehdi Ghandi, Saleh Salahi, Mohammad Hasani, “A mild, expedient, one-pot trifluoromethanesulfonic anhydride mediated synthesis of N-arylimidates”, Tetrahedron Letters, 52:2 (2011), 270
Robert D. Larsen, Ian W. Davies, Progress in Heterocyclic Chemistry, 11, A Critical Review of the 1998 Literature preceded by two Chapters on Current Heterocyclic Topics, 1999, 230
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