Department of Chemistry,Shri Durga Ji P.G. College, Chandeswhar Azamgarh, and R. P.G. College, Jamuhai, Jaunpur, U.P. (INDIA)
3-Aryl-4-amino-5-mercapto-s-triazoles (Ia-g) were prepared in excellent yield. These compounds further treating with equimolar mixture of cyanogen bromide in ethanol yielded 6-amino-3-aryl-s-triazolo- [3,4-b]-1,3,4-thiadizoles (IIa-g) which on further treating with 2,3-dichloroquinoxaline in the presence of anhydrous sodium acetate gives the title compound 3-aryl-s-triazolo [3,4-b]-1,3,4-thiadiazolo [3,2- b] imidazo [4,5-b] quinoxalines (IIIa-g). All the synthesize compounds were well characterized by their elemental and spectral studies. Fungitoxicity of the synthesized compounds were evaluated against Phytophthora infestans and Aspergillus niger.
Copy the following to cite this article:
ATMA RAM MISHRA, KASHI NATH TRIPATHI and H.C. MISHRA, "Synthesis and fungitoxicity of 3-aryl-s-triazolo-[3,4-b]-1,3,4- thiadiazolo [3,2-b] imidazo [4,5-b] quinoxalines", Journal of Ultra Chemistry, Volume 8, Issue 2, Page Number , 2016Copy the following to cite this URL:
ATMA RAM MISHRA, KASHI NATH TRIPATHI and H.C. MISHRA, "Synthesis and fungitoxicity of 3-aryl-s-triazolo-[3,4-b]-1,3,4- thiadiazolo [3,2-b] imidazo [4,5-b] quinoxalines", Journal of Ultra Chemistry, Volume 8, Issue 2, Page Number , 2016Available from: http://journalofchemistry.org/paper/401/