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Über die Hydrierung α‐cyanoäthylierter Aldimine
Author(s) -
Zondler Helmut,
Pfleiderer Wolfgang
Publication year - 1975
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19750580805
Subject(s) - aldimine , chemistry , catalysis , piperidine , intramolecular force , organic chemistry , medicinal chemistry , polymer chemistry
The catalytic hydrogenation of α‐mono‐ and bis‐cyanoethylated aldimines The catalytic hydrogenation of α‐mono‐ and ‐bis‐cyanoethylated aldimines using nickel catalysts was studied. Piperidine derivatives are formed in intramolecular cyclization reactions. The hydrogenation products of α‐bis‐cyanoethylated ketones, the decahydro‐1, 8‐naphthyridines, are observed here only as by‐products.