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Efficient syntheses of 3H-azuleno[8,1-cd]pyridazines and their thermal and photochemical reactions

✍ 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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✦ 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.


πŸ“œ SIMILAR VOLUMES


New cyclic sulfur ylides, 8-thiaazulenes
✍ Mikio Hori; Tadashi Kataoka; Hiroshi Shimizu; Mitsuhito Okitsu πŸ“‚ Article πŸ“… 1980 πŸ› Elsevier Science 🌐 French βš– 220 KB

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