Abstract
Schiff bases prepared from aromatic aldehydes and alicyclic amines undergo transimination and reduction with 3,5-dicarboethoxy-2,6-dimethyl-1,4-dihydropyridine, as thenadh model in the presence of aromatic amines in acetic acid. This sequence of steps is analogous to a similar chemical mechanism proposed for glutamate dehydrogenase. In the absence of thenadh model, only the transimination process is observed.
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Singh, S., Gill, S. & Singh, I. Transimination and reduction of imines usingnadh models. Proc. Indian Acad. Sci. (Chem. Sci.) 93, 1179–1183 (1984). https://doi.org/10.1007/BF02863622
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DOI: https://doi.org/10.1007/BF02863622