Ketoken gem-dithiols and trithiones: Synthesis and study of the behavior towards dipole reagents; Synthesis of some nitrogen heteroaromatics

Article abstract of DOI:10.1080/10426509608029632

The behavior of ketoken gem-dithiols towards active methylene and methyl groups resulted in the formation of thiopyrano-dihydrocaumarine derivatives IIIa,b via cyclocondensation reaction between substituted 4-dihydrocyclohexanone Ia.b. N-phenylpyrazoline

Full text of DOI:10.1080/10426509608029632

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Phosphorus, Sulfur, and Silicon and
the Related Elements
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KETOKEN GEM-DITHIOLS AND
TRITHIONES: SYNTHESIS AND STUDY
OF THE BEHAVIOR TOWARDS DIPOLE
REAGENTS; SYNTHESIS OF SOME
NITROGEN HETEROAROMATICS
Salem E. Zayed a
a Department of Chemistry, Faculty of Science , South Valley
University , Kena, 83511, Egypt
Published online: 24 Sep 2006.
To cite this article: Salem E. Zayed (1996) KETOKEN GEM-DITHIOLS AND TRITHIONES:
SYNTHESIS AND STUDY OF THE BEHAVIOR TOWARDS DIPOLE REAGENTS; SYNTHESIS OF SOME
NITROGEN HETEROAROMATICS, Phosphorus, Sulfur, and Silicon and the Related Elements,
108:1-4, 7-13, DOI: 10.1080/10426509608029632
To link to this article: http://dx.doi.org/10.1080/10426509608029632
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