4.5 Article

Synthesis and Antioxidant and Antitumor Activity of Novel Pyridine, Chromene, Thiophene and Thiazole Derivatives

Journal

ARCHIV DER PHARMAZIE
Volume 345, Issue 5, Pages 378-385

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ardp.201100335

Keywords

2-Tosylacetonitrile; Arylidenes; Antioxidant and antitumor activities; a-Halo compounds; Thiocarbamoyl

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2-Tosylacetonitrile (1) when reacted with a,beta-unsaturated nitriles 2ac or a mixture of formaldehyde and 3-amino-2-substituted-pent-2-endinitriles 6a,b yielded pyridine derivatives 3ac and 9a,b, respectively, while when subjected to react with salicylaldehyde yielded chromene derivatives 4 and 5, subsequently. The behavior of thiocarbamoyl derivative 10 derived from 1 towards some a-halogenated compounds have been investigated as well as its behavior towards elemental sulfur and phenyl isothiocyanate. Newly synthesized compounds were screened for their antioxidant activity, erythrocytes haemolysis and bleomycin-independent DNA damage. Some of the tested compounds exhibited promising activities.

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