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Synthesis of hindered spiro-oxindoles by photolysis of 1-(1-alkenyl)benzotriazoles

โœ 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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โœฆ 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.


๐Ÿ“œ SIMILAR VOLUMES


A Synthesis of spiro[oxindole-3,2โ€ฒ-bicyc
โœ C.G. Richards; M.S.F. Ross ๐Ÿ“‚ Article ๐Ÿ“… 1968 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 160 KB

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