Ultraviolet irradiation of 2,4-dimethyl-4- dichloromethyl-cyclohexa-2,5-dienone-1
β Scribed by E.E. van Tamelen; K. Kirk; G. Brieger
- Publisher
- Elsevier Science
- Year
- 1962
- Tongue
- French
- Weight
- 206 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
DISCOVERY of the profound molecular changes involved in the photodhemical conversion of santonin (I) to photosantonic acid (II),l the structure of n which was established in this Laboratory," prompted broader investigation I i1 of carboxylic acid production by ultraviolet irradiation of cross-conjugated dienones. The abnormal Reimer-Tiemann reaction product III represents an interesting variant; and we have now found that this dienone is transformed 0 c&3 0 I I I&c cm12 III la F. Radt (Editor), Elsevier's Encvclooedia of Oraanic Chemistry vol.
π SIMILAR VOLUMES
The anodic methoxylation cd':, series of alkylbiphenyls (2-, 3-, 4-methylbiphenyl, 3,3'-, 4,4'-dimethylhiphenyl, 4-ethylbiphenyl and 4,4'-di-tea-butylhiphenyl) carried out under constant current intensity afforded, in a process of two electrons, a number of ci.s/trum cyclohexa-l,4-dienes and, in a p