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

Electron Aleksandrovich Mistryukov 1
Electron Aleksandrovich Mistryukov
, 
Olga N Sorokina 1
Olga N Sorokina
10.1070/MC1998v008n04ABEH000955
Published 1998-09-10
Communication , Volume 8, Issue 4, 153-154
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Mistryukov E. A., Sorokina O. N. On the nature of the intermediate in the Lewis acid-promoted synthesis of dihydroisoquinolines from nitriles and β-phenylethyl chloride // Mendeleev Communications. 1998. Vol. 8. No. 4. pp. 153-154.
GOST all authors (up to 50) Copy
Mistryukov E. A., Sorokina O. N. On the nature of the intermediate in the Lewis acid-promoted synthesis of dihydroisoquinolines from nitriles and β-phenylethyl chloride // Mendeleev Communications. 1998. Vol. 8. No. 4. pp. 153-154.
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TY - JOUR
DO - 10.1070/MC1998v008n04ABEH000955
UR - https://mendcomm.colab.ws/publications/10.1070/MC1998v008n04ABEH000955
TI - On the nature of the intermediate in the Lewis acid-promoted synthesis of dihydroisoquinolines from nitriles and β-phenylethyl chloride
T2 - Mendeleev Communications
AU - Mistryukov, Electron Aleksandrovich
AU - Sorokina, Olga N
PY - 1998
DA - 1998/09/10
PB - Mendeleev Communications
SP - 153-154
IS - 4
VL - 8
ER -
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@article{1998_Mistryukov,
author = {Electron Aleksandrovich Mistryukov and Olga N Sorokina},
title = {On the nature of the intermediate in the Lewis acid-promoted synthesis of dihydroisoquinolines from nitriles and β-phenylethyl chloride},
journal = {Mendeleev Communications},
year = {1998},
volume = {8},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1998v008n04ABEH000955},
number = {4},
pages = {153--154},
doi = {10.1070/MC1998v008n04ABEH000955}
}
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Mistryukov, Electron Aleksandrovich, and Olga N Sorokina. “On the nature of the intermediate in the Lewis acid-promoted synthesis of dihydroisoquinolines from nitriles and β-phenylethyl chloride.” Mendeleev Communications, vol. 8, no. 4, Sep. 1998, pp. 153-154. https://mendcomm.colab.ws/publications/10.1070/MC1998v008n04ABEH000955.

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.

References

2.
10.1070/MC1998v008n04ABEH000955_bib2
Schclyaev
Khim. Geterotsikl. Soedin., 1987