## Abstract magnified image Disubstituted 1,2,4βoxadiazoles have been synthesized in good yields and good purity in one pot procedure by reaction of aromatic nitriles, hydroxylamine hydrochloride and sodium carbonate in ethylene glycol under heating at 195Β°C. The structures of different 1,2,4βoxad
β¦ LIBER β¦
A novel reaction of (ferrocenylmethyl)trimethylammonium iodide. One step synthesis of 3-ferrocenyl-5-alkyl-1,2,4-oxadiazoles
β Scribed by Tadao Kondo; Keiji Yamamoto; Hidenori Danda; Makoto Kumada
- Book ID
- 108347030
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- English
- Weight
- 212 KB
- Volume
- 61
- Category
- Article
- ISSN
- 0022-328X
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