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- W2058407793 abstract "High field (360 MHz) 1H NMR studies have shown that the conformation of ring C in the oxymorphamines is dramatically influenced by the stereochemistry of the 6-amino group: ring C exists in a chair conformation in the 6β-epimer but adopts a twist boat conformation in the 6α-epimer." @default.
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- W2058407793 date "1983-01-01" @default.
- W2058407793 modified "2023-09-27" @default.
- W2058407793 title "Solution conformations of the 6α and 6β epimers of oxymorphamine" @default.
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- W2058407793 doi "https://doi.org/10.1016/s0040-4039(00)94011-5" @default.
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