✦ LIBER ✦

Study of the reactions of 3-chloro-4-cyanobenzo[b][1,6]naphthyridine with nucleophilic reagents

✍ Scribed by A. S. Ivanov; N. Z. Tugusheva; N. P. Solov"eva; V. G. Granik

Book ID: 110409747
Publisher: Springer
Year: 2002
Tongue: English
Weight: 463 KB
Volume: 51
Category: Article
ISSN: 1573-9171
DOI: 10.1023/a:1021636632164

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Study of the Reactions of 3-Chloro-4-cya

Study of the Reactions of 3-Chloro-4-cyanobenzo[b][1,6]naphthyridine with Nucleophilic Reagents.

✍ A. S. Ivanov; N. Z. Tugusheva; N. P. Solov'eva; V. G. Granik 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 214 KB 👁 1 views

Reactions of 4-methyl(chloro)sulfonyl-2,

Reactions of 4-methyl(chloro)sulfonyl-2,3,5,6-tetrabromopyridines with nucleophilic reagents

✍ S. D. Moshchitskii; A. A. Zeikan' 📂 Article 📅 1979 🏛 Springer US 🌐 English ⚖ 575 KB

Reaction of 6-sulfonyl-2,3-dichloro-1,4-

Reaction of 6-sulfonyl-2,3-dichloro-1,4-naphthaquinones with nucleophilic reagents

✍ R. P. Shishkina; V. I. Mamatyuk; L. V. Éktova; E. P. Fokin 📂 Article 📅 1985 🏛 Springer 🌐 English ⚖ 602 KB

Synthesis of 6-Methylbenzo[b]pyrido[3,2-

Synthesis of 6-Methylbenzo[b]pyrido[3,2-f][1,6]naphthyridines from 4-Chloro-2-methylquinoline.

✍ T. Suresh; R. Nandha Kumar; P. S. Mohan 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 23 KB 👁 1 views

The First Synthesis of Furazano[3,4-b][1

The First Synthesis of Furazano[3,4-b][1,6]naphthyridines.

✍ Leonid S. Vasilev; Aleksei B. Sheremetev; Vladimir A. Dorokhov; Kyrill Yu. Supon 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 21 KB 👁 2 views

The first synthesis of furazano[3,4-b][1

The first synthesis of furazano[3,4-b][1,6]naphthyridines

✍ Leonid S. Vasilev; Aleksei B. Sheremetev; Vladimir A. Dorokhov; Kyrill Yu. Supon 📂 Article 📅 2007 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 462 KB

## Abstract magnified image Reaction of 6‐acetyl‐7‐aminofurazano[3,4‐__b__]pyridines with DMFDMA afforded __N__,__N__‐dimethylformamidines that were cyclized to the novel furazan‐fused [1,6]naphthyridine system by treatment with sodium methylate in good yield. The tricyclic system is characterized