✦ LIBER ✦

Halogenation and Dehalogenation of the 2,7-Naphthyridine Ring.

✍ Scribed by Eugen Barbu; Flavian Cuiban

Publisher: John Wiley and Sons
Year: 2010
Weight: 28 KB
Volume: 33
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200250112

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Thiocyanation, Halogenation, Dehalogenat

Thiocyanation, Halogenation, Dehalogenation, Transhalogenation, and Nitration of 2-Substituted 4-(2-Furyl)thiazoles.

✍ N. O. Saldabol; J. Popelis; V. Slavinska 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 145 KB

Elaboration of 1,8-Naphthyridine-2,7-Dic

Elaboration of 1,8-Naphthyridine-2,7-Dicarboxaldehyde into Novel 2,7-Dimethylimine Derivatives.

✍ Choua Vu; DeeDee Walker; Jason Wells; Stephen Fox 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

The first synthesis of the benzo[b]indol

The first synthesis of the benzo[b]indolo[1,2-h][1,7]naphthyridine ring system

✍ Olga V. Baranova; Maxim E. Zhidkov; Sergey V. Dubovitskii 📂 Article 📅 2011 🏛 Elsevier Science 🌐 French ⚖ 190 KB

First Total Synthesis of the 2,7-Naphthy

First Total Synthesis of the 2,7-Naphthyridine Alkaloids Lophocladine A and B.

✍ Matthias Lotter; Johannes Schilling; Eberhard Reimann; Franz Bracher 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 17 KB

First Total Synthesis of the 2,7-Naphthy

First Total Synthesis of the 2,7-Naphthyridine Alkaloids Lophocladine A and B

✍ Matthias Lotter; Johannes Schilling; Eberhard Reimann; Franz Bracher 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 298 KB 👁 2 views

## Abstract The one‐pot reaction of 4‐benzylpyridine‐3‐carbonitrile with Bredereck's reagent and subsequent treatment with either glacial acetic acid and sulfuric acid or ammonium acetate provided the new bioactive naphthyridine alkaloids lophocladine A and B, respectively.

The amination of halogeno-2,7- and 1,8-n

The amination of halogeno-2,7- and 1,8-naphthyridines

✍ H. J. W. van den Haak; H. C. van der Plas 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 366 KB