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Dual reactivity of 1,2-disubstituted dihydro-N-heteroaromatic systems. 2. Mechanism of the dehydrogenation of N-acyldihydroquinolines and isoquinolines with 2,2,6,6-tetramethyl-1-oxopiperidinium perchlorate

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The mechanism of the heterolytic dehydrogenation of various N-acyl derivatives of α-substituted 1,2-dihydroquinolines and isoquinolines with 2,2,6,6-tetramethyl-1-oxopiperidinium perchlorate was investigated.

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See [1] for Communication 1.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 78–84, January, 1981.

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Skorobogatova, Z.M., Golubev, V.A. & Sheinkman, A.K. Dual reactivity of 1,2-disubstituted dihydro-N-heteroaromatic systems. 2. Mechanism of the dehydrogenation of N-acyldihydroquinolines and isoquinolines with 2,2,6,6-tetramethyl-1-oxopiperidinium perchlorate. Chem Heterocycl Compd 17, 63–69 (1981). https://doi.org/10.1007/BF00507094

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  • DOI: https://doi.org/10.1007/BF00507094

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