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- W1506604449 abstract "The two compounds were labelled by 14C on the hydroxyimino methyl group substituted on the 2 positions of the pyridinium ring. The convenient pyridinium lithiated intermediates were formylated with N-methyl 14C-formanilide. The hydroxyimino methyl groups were synthezised by reaction of the 14C-formyl compound with hydroxylamine. For the two species alkylation of pyridine was performed with methyliodide. Radiochemical yields were 50% and 20%." @default.
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- W1506604449 date "1990-12-01" @default.
- W1506604449 modified "2023-09-25" @default.
- W1506604449 title "Synthese radioactive de sels d'ammonium quaternaires d'hydroxy imino methyl-2 OU -4 pyridinyle par l'intermediaire de la N-methyl formanilide-14C. II. Marquage par 14C de l'iodure d'[hydroxyimino methyl-2 methyl-1 pyridinyle ou 2-PAM Iodure et du diodure" @default.
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- W1506604449 doi "https://doi.org/10.1002/jlcr.2580281205" @default.
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