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Novel Ring Contraction of 6-Azauracil Derivatives

✍ Scribed by Hanna Wojtowicz-Rajchel; Joanna Szczepkowska-Sztolcman; Andrzej Katrusiak; Krzysztof Golankiewicz


Book ID
104202821
Publisher
Elsevier Science
Year
2000
Tongue
French
Weight
124 KB
Volume
56
Category
Article
ISSN
0040-4020

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✦ Synopsis


21008C with and without an electrophilic agent. Reactions of appropriate 6-azauracils with t-butyllithium and lithium diisopropylamide gave, as a result of a ring contraction, compounds 5 and 6. The structure of compound 5 was undeniably established by X-ray analysis. A mechanism of the novel ring transformation of 1,2,4-triazines to imidazoles is discussed.


📜 SIMILAR VOLUMES


1-Aryl-6-azauracils, XXXVI1): Synthesis
✍ Jan Slouka; Miloslav Hejsek 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 192 KB

In spite of the fact that a great number of several 4-substituted derivatives of phenazone has already been prepared, the only derivative with 6-azauracile cycle up to now is 4-(2-thio-6-azauraciI-5-yl)-phenazone, prepared by Schmid?'.

Synthesis of some isomeric quinoxaline d
✍ Iveta Wiedermannová; Jan Slouka 📂 Article 📅 2001 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 37 KB

## Abstract By diazotization of 3‐(2‐aminophenyl)‐1,2‐dihydroquinoxaline 1c, its 3‐(4‐aminophenyl)‐isomer**2c**, 3‐(2‐aminobenzyl)‐1,2‐dihydroquinoxaline‐2‐one **3c** and its 3‐(4‐aminobenzyl)‐isomer **4c** and by azo coupling of formed diazonium salts with ethyl cyanoacetylcarbamate, corresponding