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Photochemical rearrangements of cross-conjugated cyclohexadienones. Application to the synthesis of (-)-4-epiglobulol and (+)-4-epiaromadendrene

โœ Scribed by Caine, Drury S.; Gupton, John T.


Book ID
127266353
Publisher
American Chemical Society
Year
1975
Tongue
English
Weight
314 KB
Volume
40
Category
Article
ISSN
0022-3263

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Photochemical rearrangements of cross-co
โœ Paul J. Kropp; William F. Erman ๐Ÿ“‚ Article ๐Ÿ“… 1963 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 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