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Davalian et al., 1979 - Google Patents

Synthesis of 7, 8-epoxy-7, 8-dihydroretinoids

Davalian et al., 1979

Document ID
8712162532272743268
Author
Davalian D
Heathcock C
Publication year
Publication venue
The Journal of Organic Chemistry

External Links

Snippet

10 substance is converted by anhydrous HBr in ether into crystalline E, E bromo ester 8 (54%). Compound 8 reacts with triethyl phosphite at 130-140 C to provide phosphonate 9 in quantitative yield. The anion of 9 reacts with the known ß-ionone epoxide 10, 7 8 furnishing …
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    • C07C2101/16The ring being unsaturated
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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C403/00Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
    • C07C403/14Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by doubly-bound oxygen atoms
    • C07C403/16Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by doubly-bound oxygen atoms not being part of -CHO groups
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