Chemistry of Heterocyclic Compounds p. 410 - 414 (1986)
Update date:2022-08-03
Topics: Derivative Formation Experimental conditions Hantzsch synthesis 3,3,5-Tricarbonyl-1,2,3,4-tetrahydropyridine
Chekavichus, B.S.
Sausin, A.E.
Zolotoyabko, R.M.
Liepin'sh, E.E.
Mazheika, I.B.
Dubur, G.Ya.
An ester of p-nitrobenzoylacetic acid is cyclized under the action of hexamethylentetramine and ammonium acetate to 3,5-diethoxycarbonyl-3-p-nitrobenzoyl-6-p-nitrophenyl-1,2,3,4-tetra-hydropyridine, the structure of which has been established by NMR, UV,
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