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Etude du metabolisme de l'hydroxy3 hydroxy methyl5 methyl2 isonicotin-aldoxime, de l'hydroxy2 methoxy3 benzaldoxime et de la dioxime hydroxy4 methoxy5 isophtalique

✍ Scribed by Pham-Huu-Chanh; Som Chanvattey; J. Patte

Book ID
115770459
Publisher
Elsevier Science
Year
1970
Tongue
English
Weight
403 KB
Volume
19
Category
Article
ISSN
0006-2952

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The two compounds were labelled by ^14^C on the hydroxyimino methyl group substituted on the 2 positions of the pyridinium ring. The convenient pyridinium lithiated intermediates were formylated with N‐methyl ^14^C‐formanilide. The hydroxyimino methyl groups were synthezised by reaction of the ^14^