ChemInform Abstract: Antitumor Polycyclic Acridines. Part 5. Synthesis of 7H-Pyrido[4,3,2-kl]acridines with Exploitable Functionality in the Pyridine Ring.
β Scribed by M. JULINO; M. F. G. STEVENS
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 40 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Antitumor Polycyclic Acridines. Part 5. Synthesis of 3,2kl]acridines with Exploitable Functionality in the Pyridine Ring. -In continuation of the program concerning the development of a new anticancer polycyclic acridine, a novel route to such compounds is presented. The advantage is the formation of a single triazolylacridine. A further cyclization to (X) is achieved if R 2 is a corresponding chlorobutyl side chain. -(JULINO, M.;
π SIMILAR VOLUMES
## 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