The new and simple ‘LEGO’ system: Its application for the synthesis of 6-oligopyridyl-1,5,12-triazatriphenylenes
✍ Scribed by Gunther R. Pabst; Oliver C. Pfu¨ller; Ju¨rgen Sauer
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 178 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The condensation of 1,10-phenanthroline-5,6-dione 1 with amidrazones 2 leads to 6-hetaryl-substituted 1,2,4,8,9-pentaazatriphenylenes 3. These condensed 1,2,4-triazines can be easily transformed to pyridines by [4+2] cycloaddition with norborna-2,5-diene followed by [4+2] cycloreversions of nitrogen and cyclopentadiene. This reaction sequence offers a new, simple and general access to 6-oligopyddyl-l,5,12-triazatriphenylenes 4.
📜 SIMILAR VOLUMES
The condensation of pyridine-2,4,6-tricarboxtrisamidrazone 1 with 1,2-dicarbonyl compounds 2 -3 leads to trisubstituted 1,2,4-triazines 4 -6. These 1,2,4-triazines can be easily transformed to superbranched pyridines 7 -9 by [4+2] cycloaddition with norborna-2,5-diene followed by [4+2] cycloreversio
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