Azo Coupling of Enamino Amides of the 3,3-Dimethyl-1,2,3,4-tetrahydroisoquinoline Series with Arenediazonium Salts


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The azo coupling of arenediazonium chlorides with (Z)-2-(3,3-dimethyl-3,4-dihydroisoquinolin-1(2H)-ylidene)-N-(4-methylphenyl)acetamide afforded (Z)-2-(2-arylhydrazinylidene)-2-(3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)-N-(4-methylphenyl)acetamides whose structure was confirmed by 1H NMR and X-ray diffraction data. The azo coupling products containing no p-tolyl substituent on the amide nitrogen atom exist in solution as mixtures of azo and hydrazone tautomers. Electronic absorption spectra of the synthesized compounds were studied.

作者简介

A. Mikhailovskii

Perm State Pharmaceutical Academy

编辑信件的主要联系方式.
Email: neorghim@pfa.ru
俄罗斯联邦, Perm

E. Pogorelova

Perm State Pharmaceutical Academy

Email: koh2@psu.ru
俄罗斯联邦, Perm

N. Pershina

Perm State Pharmaceutical Academy

Email: koh2@psu.ru
俄罗斯联邦, Perm

E. Lyust

Perm State Pharmaceutical Academy

Email: koh2@psu.ru
俄罗斯联邦, Perm

M. Dmitriev

Perm National State Research University

编辑信件的主要联系方式.
Email: koh2@psu.ru
俄罗斯联邦, Perm

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