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- W2029694501 abstract "(6aR)-1,2-(Methylenedioxy)aporphine-10, 11-diol (8) and (6aR)-aporphine-1, 1, 10, 11-tetrol (16) have been prepared from natural (S)-bulbocapnine (4). For both compounds, the partial synthesis included racemic intermediates which have been resolved into their enantiomers. Both compounds 8 and 16 showed dopaminergic activity in rats, although to a lower extent than (R)-apomorphine (1) itself." @default.
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- W2029694501 date "1979-07-17" @default.
- W2029694501 modified "2023-09-25" @default.
- W2029694501 title "Conversion of Natural (S)-Bulbocapnine into Two (Ring A)-Substituted Derivatives of (R)-Apomorphine" @default.
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- W2029694501 doi "https://doi.org/10.1002/hlca.19790620519" @default.
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