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ChemInform Abstract: Antitumor Polycyclic Acridines. Part 5. Synthesis of 7H-Pyrido[4,3,2-kl]acridines with Exploitable Functionality in the Pyridine Ring.

✍ 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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✦ 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.;


πŸ“œ SIMILAR VOLUMES


Antitumor Polycyclic Acridines. Part 13.
✍ Michael J. Ellis; Malcolm F. G. Stevens πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons βš– 108 KB πŸ‘ 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