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- W143472419 endingPage "170" @default.
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- W143472419 abstract "The aporphine alkaloids are one of the largest groups within the isoquinoline alkaloids (Shamma 1972, Fig. 1). In the naturally occurring aporphine alkaloids, positions 1 and 2 are always oxygenated and frequently other positions are also substituted with hydroxyl, methoxyl or methylenedioxy groups. In a few cases a hydroxyl function is located at C-7, while in the case of steporphine, oxygenation is at C-4. Glaucine and bulbocapnine were among the first naturally occurring aporphines to have their structures elucidated (Manske 1954) and usually the natural alkaloids have proved to be optically active, possessing either the R or S absolute configuration. For a recent review of aporphine biosynthesis see Shamma and Guinaudeau, 1984." @default.
- W143472419 created "2016-06-24" @default.
- W143472419 creator A5049508440 @default.
- W143472419 date "1985-01-01" @default.
- W143472419 modified "2023-09-27" @default.
- W143472419 title "Synthesis and Structure-Activity Relationships of Aporphines as Dopamine Receptor Agonists and Antagonists" @default.
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- W143472419 doi "https://doi.org/10.1007/978-3-642-70128-3_10" @default.
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