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ChemInform Abstract: Antitumor Polycyclic Acridines. Part 3. A Two-Step Conversion of 9-Azidoacridine to 7H-Pyrido[4,3,2-kl]acridines by Graebe—Ullmann Thermolysis of Substituted 9-(1,2,3-Triazol-1-yl)acridines.

✍ Scribed by D. J. HAGAN; D. CHAN; C. H. SCHWALBE; M. F. G. STEVENS

Publisher
John Wiley and Sons
Year
2010
Weight
35 KB
Volume
29
Category
Article
ISSN
0931-7597

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📜 SIMILAR VOLUMES

Antitumor Polycyclic Acridines. Part 13.
Antitumor Polycyclic Acridines. Part 13. Synthesis of 2-Substituted 7H-Pyrido[4,3,2-kl]acridines by Thermolysis of 9-(5-Alkyltriazol-1-yl)acridines.
✍ Michael J. Ellis; Malcolm F. G. Stevens 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 108 KB 👁 1 views

## Fused pyridine derivatives R 0450 Antitumor Polycyclic Acridines. Part 13. Synthesis of 2-Substituted 7H-Pyrido[4,3,2-kl]acridines by Thermolysis of 9-(5-Alkyltriazol-1-yl)acridines. -Reaction of phosphoranylidene ketones (I) with 9-azidoacridine (II) affords 9-triazolylacridines (III), which on