E. A. Mistryukov, O. N. Sorokina, A. E. Mistryukov, “Lewis acid mediated cyclisation of β-phenylethylamides with an unactivated benzene ring: an efficient preparation of dihydroisoquinolines”, Mendeleev Commun., 6:6 (1996), 39

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Mendeleev Communications, 1996, Volume 6, Issue 6, Pages 39–241
DOI: https://doi.org/10.1070/MC1996v006n06ABEH000741 (Mi mendc4983)

This article is cited in 3 scientific papers (total in 3 papers)

Lewis acid mediated cyclisation of β-phenylethylamides with an unactivated benzene ring: an efficient preparation of dihydroisoquinolines

E. A. Mistryukov^a, O. N. Sorokina^a, A. E. Mistryukov^b

^a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
^b N.S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Full-text PDF (425 kB) Citations (3)

DOI: https://doi.org/10.1070/MC1996v006n06ABEH000741

Abstract: The efficient Lewis acid assisted cyclisation of β-phenylethylamide into dihydroisoquinolines was optimised in relation to metal chloride catalyst, and by X-ray crystallography a new type of non-bonded interaction in the cyclic systems was demonstrated: face coordination of the Cl-anion and an electron deficient pyridinium π-system.

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Document Type: Article

Language: English

Citation: E. A. Mistryukov, O. N. Sorokina, A. E. Mistryukov, “Lewis acid mediated cyclisation of β-phenylethylamides with an unactivated benzene ring: an efficient preparation of dihydroisoquinolines”, Mendeleev Commun., 6:6 (1996), 39–241

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https://www.mathnet.ru/eng/mendc/v6/i6/p39

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