ISSN:
1573-8353
Source:
Springer Online Journal Archives 1860-2000
Topics:
Chemistry and Pharmacology
Notes:
Abstract On the basis of the spectral data (1H and 13C NMR, measurements of the nuclear Overhauser effect (NOE) and t1, UV spectra), the structure of tricyclic compounds formed in the condensation of substituted o-phenylenediamines with 3,4,6-trichloropyridazine, as well as two types of isomeric products of their alkylation, was established; tautomerism and protonation of the compounds obtained were studied.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00505723
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