Syntheses with stable isotopes: Benzidine-15N2
Benzidine‐15N2 was prepared from 4,4′‐biphenyldicarboxamide‐15N2 by the Hofmann amide degradation. The diamide, in turn, was obtained from 4,4′‐biphenyldicarbonyl chloride and ammonium‐15N sulfate. An overall yield of 30–35% was obtained for the two steps. An attempted synthesis of N‐hydroxybenzidin...
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Veröffentlicht in: | Journal of labelled compounds & radiopharmaceuticals 1978, Vol.14 (2), p.243-248 |
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Sprache: | eng |
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