Affiliation:
1. Institut für Organische Chemie der Universität in Graz
Abstract
N,N′-Dimethyl-5-anilinomethylene-barbituric acids and its thio analogues react with alkyl cyanoacetates or malodinitrile in DMF in the presence of KOH to give 1,2,3,4- Tetrahydro-7 H-pyrano[2,3-d]pyrimidines, whereas N-unsubstituted anilinomethylenebarbituric acids under the same conditiones afford 1,2,3,4-tetrahydro-pyrimidine-5-propenoic acid derivatives.
Cited by
12 articles.
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2. References;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
3. Intermolecular double Michael reaction to construct 4-benzyl-5-imino-3-phenyl-6-oxa-1-aza-tricyclo[6.2.2.02,7]dodec-2(7)-ene-4-carbonitrile;Journal of Chemical Research;2005-10
4. Synthesis of novel fluorinated derivatives of 1,3-dimethylbarbituric acid;Tetrahedron;1998-06
5. A convenient synthesis of 1,3-diaryl-1,2,3,4,-tetrahydro-5,7,7-trimethyl-4-oxo-2-thioxo-7H-pyrano[ 2 ,3-d ]pyrimidines;Tetrahedron;1990-01