Efficient syntheses of 3H-azuleno[8,1-cd]pyridazines and their thermal and photochemical reactions
β Scribed by Chi-Phi Wu; Rammohan Devulapally; Tsung-Chieh Li; Chien-Kuo Ku; Hsien-Chung Chung
- Book ID
- 104098045
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 722 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Azulenopyridazines 6 were efficiently synthesized from ethyl 4-hydrazinylazulene-1-carboxylate (2) by p-toluenesulfonic acid-catalyzed imine formation and intramolecular cyclization followed by dehydrogenation using KOH/MeOH in one-pot operation. Thermal and photochemical reactions of azulenopyridazines 6 afforded 1-vinylazulenes 7 in good yields.
π SIMILAR VOLUMES
A new cyclic sulfur ylide, 1,3-diphenyl-8-methyldibenzo[e,h]-8-thiaazulene was synthesized. 8-Alkyl-1,3-diphenyldibenzo[e,h]-8-thiaazulenes were thermally rearranged to give l,Z-rearranged products and 1,4-rearranged products. In the course of our studies on thiaazulenylium salts, 2) we have reporte