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Oxidative formation and photochemical isomerization of spiro-epoxy-2,4-cyclohexadienones

✍ Scribed by Hans-Dieter Becker; Torbjorn Bremholt; Erich Adler


Book ID
104245357
Publisher
Elsevier Science
Year
1972
Tongue
French
Weight
176 KB
Volume
13
Category
Article
ISSN
0040-4039

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✦ Synopsis


The oxidation of salicylalcohol (I; R=R'=H) by sodium periodate was recently reported to give a dehydrodimer by spontaneous Diels-Alder reaction of the intermediary Spiro-epoxy-2,4-cyclohexadienone II (R=R'=H). Analogous


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✍ Paul J. Kropp; William F. Erman πŸ“‚ Article πŸ“… 1963 πŸ› Elsevier Science 🌐 French βš– 237 KB

IT is well established that 4-ntethylcyclohexadienones of the santonin type undergo photochemical transformation in aqueous acetic acid to perhydroasulene derivatives of the isophotosantonic la&one type.' The photochemical properties of cyclohexadienones which are unsubstituted at C4 have also been