Bachmann et al., 1951 - Google Patents
Synthesis of Isoequilenin via the Diels-Alder Reaction. The Configuration of the C/D Ring Juncture of the Estrogenic HormonesBachmann et al., 1951
- Document ID
- 8141002686169954480
- Author
- Bachmann W
- Controulis J
- Publication year
- Publication venue
- Journal of the American Chemical Society
External Links
Snippet
The Diels-Alder reaction of l-vinyl-6-methoxy-3, 4-dihydronaphthalene with mesaconic acid yielded two structurally isomeric adducts, the structures and configurations of which were established. The anhydride adduct formed from maleic anhydride and the diene, the …
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 OC1=CC=C2C(CCC3(C4CCC3=O)C)=C4C=CC2=C1 0 title abstract description 8
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- C—CHEMISTRY; METALLURGY
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- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D307/87—Benzo [c] furans; Hydrogenated benzo [c] furans
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- C—CHEMISTRY; METALLURGY
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- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
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- C—CHEMISTRY; METALLURGY
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