The thermally induced rearrangement of 1-substituted imidazoles
β Scribed by Begg, CG; Grimmett, MR; Wethey, PD
- Book ID
- 121308492
- Publisher
- Commonwealth Scientific and Industrial Research Organisation Publishing
- Year
- 1973
- Tongue
- English
- Weight
- 661 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0004-9425
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π SIMILAR VOLUMES
Indirect electrochemical reabction, by mew of aromatic anion radical mediators, of petjluoroalkyl halides in the presence of imidazolate or of substituted imidazolate anions yields the corresponding perfuoroalkylated imidazoles along an S& mechanism.
3-(Phenyliminomethyl)-and 3-arylazo-2,1-benzisoxaaoles undergo thermal rearrangement to 3-phenylquinazolin-4-one and 3-aryl-1,2,3-benzotriazin-4-ones, respectively. In a recent letter' the thermal rearrangements of some 3-(8-styryl)-2,1-benzisoxazoles (1; X=Y=CH) to 3-aryl-4-quinolones and 2-arylid