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Photocycloaddition of ethylvinylether and cyclopentene to 3.5-dimethylanisole

✍ Scribed by A.W.H. Jans; J.J. van Dijk-Knepper; J. Cornelisse; C. Kruk

Publisher
Elsevier Science
Year
1982
Tongue
French
Weight
231 KB
Volume
23
Category
Article
ISSN
0040-4039

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✦ Synopsis

Photocycloaddition of ethylvinylether and cyclopentene to 3,5-dimethylanisole yields derivatives of 1-methoxy-2,4-dimethyltricyclo[3.3.0.0 2y8]oct-3-ene in which the substituents at positions 6 and/or 7 are endo.

πŸ“œ SIMILAR VOLUMES

The meta-photocycloaddition of cyclopent
The meta-photocycloaddition of cyclopentene to ortho-methylanisole
✍ A. W. H. Jans; J. Cornelisse πŸ“‚ Article πŸ“… 2010 πŸ› Elsevier Science 🌐 English βš– 255 KB

## Abstract Photocycloaddition of cyclopentene to __ortho__‐methylanisole yields two products. The addition takes place at the positions __ortho__ with respect to the methoxy group.