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Schiff bases. Part III. Amine and ketone exchange reactions with Schiff bases
Journal of the Chemical Society C: Organic, 1968Certain ketimines of the type R12 CN–CHR22 undergo amine exchange when heated with diphenylmethylamine to give the ketimines R12CN–CHPh2, which rearrange to the tautomers R12CH–NCPh2. These undergo a second amine exchange with the production of N-(diphenylmethylene)diphenylmethylamine.
Alexander Lawson, J. O. Stevens
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Spectroscopy of non-aromatic Schiff bases
Journal of Photochemistry, 1981Abstract The photoelectron and vapour phase UV absorption spectra of a number of non-conjugated and conjugated imines, their oximes and O -methyloximes were determined. The assignment of the bands of lowest frequency is discussed as well as the nature of the primary steps that may occur in the related excited states ((π,π * ), (n,π * and Rydberg ...
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This chapter provides an engaging overview of Schiff bases, highlighting their versatility in various chemical applications. Covering the synthesis, structural diversity, and multifaceted reactivity of Schiff bases, the introduction delves into their significance in coordination chemistry, bioinorganic systems, and medicinal chemistry.
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Schiff bases containing quinoline rings
Journal of Medicinal Chemistry, 1968C T, Bahner +2 more
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Decarboxylation of Schiff bases
Journal of the American Chemical Society, 1973Kazuo. Taguchi, F. H. Westheimer
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