Chemischer Informationsdienst. Organische Chemie
 1970
DOI: 10.1002/chin.197038203
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ChemInform Abstract: NATRIUM‐AMMONIAK‐RED. IN DER N‐HETEROAROMATISCHEN CHEMIE, DEHALOGENIERUNG UND DESALKYLIERUNG VON SCHWEFELHALTIGEN PYRIMIDINEN, PYRIDAZINEN UND SYMM.‐TRIAZINEN

Jacques Lannoy1,
A. Gysen2,
R. Nasielski-Hinkens3

Abstract: Die Birch‐Reduktion der Chlorpyrimidine (I), ‐triazine (III) bzw. des Chlorpyridazins (V), die Aminogruppen besitzen, führt in 25‐86%iger Ausbeute zu den dehalogenierten Produkten (II), (IV) bzw. (VI).

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