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Alkaline hydrolysis of 3-methyl-4-nitro-5-styrylisoxazole with Na18OH

โœ Scribed by P. Sarti-Fantoni; D. Donati; F. De Sio; G. Moneti


Book ID
112126240
Publisher
Journal of Heterocyclic Chemistry
Year
1980
Tongue
English
Weight
91 KB
Volume
17
Category
Article
ISSN
0022-152X

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๐Ÿ“œ SIMILAR VOLUMES


The reactivity of 3-methyl-4-nitro-5-sty
โœ Mauro F.A. Adamo; Stefano Chimichi; Francesco De Sio; Donato Donati; Piero Sarti ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 74 KB

The expected Michael adducts and spiroisoxazolines are obtained from the reaction between 3-methyl-4-nitro-5styrylisoxazole and bis-enolisable ketones. Contrary to reported data, Michael adducts are obtained in good yields only when a substoichiometric amount of base is used, whereas spiroisoxazolin