The reactivity of 3-methyl-4-nitro-5-styrylisoxazole with some bis-enolisable ketones
โ Scribed by Mauro F.A. Adamo; Stefano Chimichi; Francesco De Sio; Donato Donati; Piero Sarti-Fantoni
- Book ID
- 104251183
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 74 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
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 spiroisoxazolines were obtained as the major product when the base is present in a large excess.
๐ SIMILAR VOLUMES
## Abstract Michael addition of title compounds (I) with benzyl mercaptan (II) proceeds with good yields in the presence of piperidine.