Synthesis of hindered spiro-oxindoles by photolysis of 1-(1-alkenyl)benzotriazoles
โ Scribed by Jonathan K. Dutton; David P.M. Pleynet; A.Peter Johnson
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 736 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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โฆ Synopsis
Photolysis of I-(1-alkoxy-l-alkenyl)benzotriazoles gives moderate yields of 2-alkoxyindolenines, which can be hydrolysed to oxindoles. A side reaction leads to the formation of iminooxetanes. The formation of the 2-alkoxy-indolenines is quite insensitive to steric hindrance at the reacting centres.
๐ SIMILAR VOLUMES
A study of isatinylidene derivatives (I) as the dienophile component of a Diels-Alder reaction was undertaken with the object of obtaining spirooxindole derivatives of the type (II) of value in the synthesis of alkaloids of the Gelsemium species. No previous synthesis of this nature appears to have