202650-93-9Relevant academic research and scientific papers
Stereoselective synthesis of dihydrothiadiazinoazines and dihydrothiadiazinoazoles and their pyrolytic desulfurization ring contraction
Al-Etaibi, Alya,John, Elizabeth,Ibrahim, Maher R.,Al-Awadi, Nouria A.,Ibrahim, Yehia A.
experimental part, p. 6259 - 6274 (2011/09/19)
Intramolecular base catalyzed C-C bond formation led to exclusive stereoselective syntheses of trans-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4] thiadiazines, trans-7,8-dihydro-6H-[1,2,4]triazino[3,4-b][1,3,4]thiadiazin-4- ones, and trans-3,4-dihydro-2H-
Studies on arylmethyltriazinone derivatives-Part II. Synthesis and antifungal properties of 2-aminomethyl-4-(arylidene)amino-6-arylmethyl-3-mercapto-1, 2,4-triazin-5(4H)-ones
Holla,Gonsalves,Shivananda
, p. 93 - 96 (2007/10/03)
The preparation of twenty new 2-aminomethyl-4-(arylidene)amino-6-arylmethyl-3-mercapto-1,2,4-triazin-5(4H)- ones(4) is described. The structural elucidation of all the compounds is carried out on the basis of analytical and spectral data. The newly synthesized compounds are evaluated for their antifungal activity against Candida albicans and Paecileomyces variotti.
Synthesis of biologically active 4-amino-6-arylmethyl-3-mercapto-1,2,4-triazin-5(4H)-ones and their Schiff bases
Holla, B. Shivarama,Gonsalves, Richard,Sarojini, B. K.
, p. 943 - 946 (2007/10/03)
Three arylpyruvic acids 2 are condensed with thiocarbohydrazide (3) in aqueous ethanol to yield 4-amino-6-arylmethyl-3-mercapto-1,2,4-triazin-5(4H)-ones 4. In a modified method these title compounds 4 have also been prepared by direct condensation of the
