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- W2003487136 abstract "Abstract 3-Hydroxyflavanone oxime has been separated into syn and anti isomers and the structures of the products are proved by IR and NMR spectroscopy. NMR investigation of the acetylated oximes has shown that these compounds probably exist in a new conformation produced by the joint action of the C 3 O acetyl substituent and the presence of the CN linkage. Results obtained with 3-hydroxy-5,7,3′,4′-tetramethoxyflavanone oxime and acetylated 3-hydroxyflavanone hydrazones support these conclusions." @default.
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- W2003487136 date "1967-01-01" @default.
- W2003487136 modified "2023-09-23" @default.
- W2003487136 title "Stereochemistry of 3-hydroxy- and 3-acetoxyflavanone oximes" @default.
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- W2003487136 doi "https://doi.org/10.1016/0040-4020(67)80015-2" @default.
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