✦ LIBER ✦

13C Nmr study of 1,2,4-triazino[4,5-b]indazole derivatives

✍ Scribed by Alain Rabaron; Jean-Charles Lancelot; Daniel Maurne; Max Robba

Book ID: 112125529
Publisher: Journal of Heterocyclic Chemistry
Year: 1979
Tongue: English
Weight: 144 KB
Volume: 16
Category: Article
ISSN: 0022-152X
DOI: 10.1002/jhet.5570160112

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Étude des conditions d'accès au tétrazol

Étude des conditions d'accès au tétrazolo-1,2,3,4-[5′,1′:6,1] triazino-1,2,4-[4,5-b]indazole et au thioxo-3 triazolo-1,2,4-[2′,1′:6,1] triazino-1,2,4-[4,5-b]indazole

✍ Max Robba; Jean-Charles Lancelot 📂 Article 📅 1984 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 335 KB

Etude des conditions d'accès au triazino

Etude des conditions d'accès au triazino-1,2,4-[4,5-b] indazole

✍ Max Robba; Jean-Charles Lancelot; Daniel Maume; Alain Rabaron 📂 Article 📅 1978 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 342 KB

Synthesis and 13C-NMR study of novel pyr

Synthesis and 13C-NMR study of novel pyrazolo[5′,1′:3, 4][1, 2, 4]triazino[5, 6-d]pyrimidines

✍ Yoshihisa Kurasawa; Yumiko Kamigaki; Ho Sik Kim; Rika Futatsukawa; Megumi Kanoh; 📂 Article 📅 1989 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 228 KB

Investigation of 1,2,4-triazino [6,5-b]i

Investigation of 1,2,4-triazino [6,5-b]indole derivatives

✍ V. S. Dmitrukha; P. S. Pel'kis 📂 Article 📅 1972 🏛 Springer US 🌐 English ⚖ 183 KB

Investigation of 1,2,4-triazino [6,5-b]i

Investigation of 1,2,4-triazino [6,5-b]indole-derivatives

✍ V. S. Dmitrukha; P. S. Pel'kis 📂 Article 📅 1972 🏛 Springer US 🌐 English ⚖ 205 KB

Synthesis of some [1,2,4]triazino[5,6-b]

Synthesis of some [1,2,4]triazino[5,6-b]quinoline derivatives

✍ Jakub Stýskala; Jan Slouka; Antonín Lycka 📂 Article 📅 2002 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 38 KB

## Abstract By coupling of diazonium salts with ethyl __N__‐(4‐oxo‐1,4‐dihydroquinolin‐2‐yl)carbamate **4**, the corresponding 3‐arylazocompounds **5** were obtained. These ones were cyclized thermally or in alkaline medium to the corresponding 2‐aryl‐2,3,5,10‐tetrahydro‐[1,2,4]triazino[5,6‐__b__]q