## Abstract The synthesis of ring A substituted TAP'S starts from 5,6‐diaminoquinoxaline (II), which is condensed with n‐butylglyoxylate to give a mixture of 2‐ and 3‐hydroxy‐TAP, which reacted with POCl~3~/PCl~5~ to afford the corresponding monochlorocompound. Similarly, the condensation of II and
13C NMR spectra of 1,4,5,8-tetraazaphenanthrene derivatives
✍ Scribed by N. Defay; D. Maetens; R. Nasielski-Hinkens
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 443 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^13^C NMR spectra of 1,4,5,8‐tetraazaphenanthrene (pyrazino[2,3‐f] quinoxaline), eleven of its derivatives [2‐ and 3‐chloro, ‐methoxy and ‐(1′‐piperidino), 2,3‐dichloro, ‐dimethoxy, ‐dimethyl and ‐di(1′‐piperidino) and 9‐methoxy] and of 1,4,5,8,9,12‐hexaazatriphenylene (dipyrazino[2,3‐f: 2′,3′‐h]quinoxaline) have been assigned by {^1^H} selective decoupling experiments, correlations and additivities of substituent‐induced chemical shifts and proton–carbon coupling patterns. Assignments of proton spectra are extended.
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