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- W2162227703 abstract "The title hydrocarbon and its 11-methyl homologue have been synthesised in one-step reactions by titanium tetrachloride induced condensation of 1-naphthylacetaldehydes with the trimethysilyl enol ether of cyclopentanone in yields of the about 20%. Like the 17-ketones of this series, microsomal oxidation of these hydrocarbons occurs mainly in the five-membered ring, and not at all at the electron-rich 6,7-double bond." @default.
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- W2162227703 date "1996-12-01" @default.
- W2162227703 modified "2023-09-23" @default.
- W2162227703 title "Novel One-step Synthesis and Hepatic Microsomal Metabolism of 16,17-Dihydro-15H-cyclopenta[a]phenanthrene" @default.
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- W2162227703 doi "https://doi.org/10.1080/10406639608544676" @default.
- W2162227703 hasPublicationYear "1996" @default.
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