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Results: 1-15 |
Results: 15
A green route to the synthesis of azo compounds
Authors: Qiao, RZ Zhang, Y Hui, XP Xu, PF Zhang, ZY Wang, XY Wang, YL
Citation: Rz. Qiao et al., A green route to the synthesis of azo compounds, GREEN CHEM, 3(4), 2001, pp. 186-188
Microwave induced synthesis of 3-aryl-6-( 6-/8-substituted 4-chloroquinoline-3-yl)-s-triazolo[3,4-b]-1,3,4-thiadiazoles
Authors: Qiao, RZ Hui, XP Xu, PF Zhang, ZY Cheng, DL
Citation: Rz. Qiao et al., Microwave induced synthesis of 3-aryl-6-( 6-/8-substituted 4-chloroquinoline-3-yl)-s-triazolo[3,4-b]-1,3,4-thiadiazoles, CHIN J CHEM, 19(8), 2001, pp. 800-806
Synthesis and antibacterial activity of 3-(5-methylisoxazol-3-yl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine derivatives
Authors: Hui, XP Xu, PF Wang, Q Zhang, Q Zhang, ZY
Citation: Xp. Hui et al., Synthesis and antibacterial activity of 3-(5-methylisoxazol-3-yl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine derivatives, CHIN J CHEM, 19(10), 2001, pp. 991-995
Synthesis of 1,3,4-thiadiazole, 1,2,4-triazole and 1,3,4-oxadiazole derivatives containing 1-(p-chlorophenyl)-5-methyl-1,2,3-triazol-4-yl moiety
Authors: Sun, XW Hui, XP Chu, CH Zhang, ZY
Citation: Xw. Sun et al., Synthesis of 1,3,4-thiadiazole, 1,2,4-triazole and 1,3,4-oxadiazole derivatives containing 1-(p-chlorophenyl)-5-methyl-1,2,3-triazol-4-yl moiety, I J CHEM B, 40(1), 2001, pp. 15-19
New method for synthesis of 4-substituted benzamido-2-thioxo-2,4-thiazolidindiones
Authors: Chu, CH Xu, PF Hui, XP Zhang, ZY Liao, RA Li, ZC
Citation: Ch. Chu et al., New method for synthesis of 4-substituted benzamido-2-thioxo-2,4-thiazolidindiones, CHEM J CH U, 22(5), 2001, pp. 768-770
Synthesis and antifungal activities of omega-[4-aryl-5-(1-phenyl-5-methyl-1,2,3-triazol-4-yl)-1,2,4-triazol-3-thio]-omega-(1H-1,2,4-triazol-1-yl)acetophenones
Authors: Chu, CH Hui, XP Zhang, Y Zhang, ZY Li, ZC Liao, RA
Citation: Ch. Chu et al., Synthesis and antifungal activities of omega-[4-aryl-5-(1-phenyl-5-methyl-1,2,3-triazol-4-yl)-1,2,4-triazol-3-thio]-omega-(1H-1,2,4-triazol-1-yl)acetophenones, J CHIN CHEM, 48(1), 2001, pp. 121-125
Reactions of 4-amino-3-(1-p-chlorophenyl-5-methyl-1,2,3-triazol-4-yl)-5-mercapto-s-triazole
Authors: Sun, XW Hui, XP Chu, CH Zhang, ZY
Citation: Xw. Sun et al., Reactions of 4-amino-3-(1-p-chlorophenyl-5-methyl-1,2,3-triazol-4-yl)-5-mercapto-s-triazole, I J CHEM B, 39(10), 2000, pp. 779-782
Synthesis of 3-(R-Phenyl)-6-phenyl-7-(1H-1,2,4-triazol-1-yl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines
Authors: Hui, XP Sun, XW Chu, CH Zhang, ZY
Citation: Xp. Hui et al., Synthesis of 3-(R-Phenyl)-6-phenyl-7-(1H-1,2,4-triazol-1-yl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines, CHEM PAP-CH, 54(4), 2000, pp. 235-238
Synthesis of 6-nitrobenzimidazole derivatives
Authors: Liu, SY Hui, XP Xu, PF Zhang, ZY
Citation: Sy. Liu et al., Synthesis of 6-nitrobenzimidazole derivatives, CHEM J CH U, 21(9), 2000, pp. 1386-1390
Studies on semisynthesis and antibacterial activity of 7 beta-heterocyclocamido-3-heterothiomethyl cephalosporins
Authors: Hui, XP Hao, L Zhang, ZY Wang, Q Wang, F Guan, ZW
Citation: Xp. Hui et al., Studies on semisynthesis and antibacterial activity of 7 beta-heterocyclocamido-3-heterothiomethyl cephalosporins, CHEM J CH U, 21(12), 2000, pp. 1844-1847
Heterocyclic systems containing bridged nitrogen atom: Synthesis and antibacterial activity of 3-(2-phenylquinolin-4-yl)/3-(1-p-chlorophenyl-5-methyl-1,2,3-triazol-4-yl)-s-triazolo[3,4-b]-1,3,4-thiadiazine derivatives
Authors: Hui, XP Dong, HS Xu, PF Zhang, ZY Wang, Q Gong, YN
Citation: Xp. Hui et al., Heterocyclic systems containing bridged nitrogen atom: Synthesis and antibacterial activity of 3-(2-phenylquinolin-4-yl)/3-(1-p-chlorophenyl-5-methyl-1,2,3-triazol-4-yl)-s-triazolo[3,4-b]-1,3,4-thiadiazine derivatives, J CHIN CHEM, 47(5), 2000, pp. 1115-1119
An interesting isomerization: Synthesis of mesoionic 5-arylamino-1,3,4-thiadiazolium-2-thiolates by using omega-bromo-omega-(1H-1,2,4-triazol-1-yl)acetophenone as catalyst
Authors: Chu, CH Hui, XP Xu, PF Zhang, ZY Li, ZC Liao, RA
Citation: Ch. Chu et al., An interesting isomerization: Synthesis of mesoionic 5-arylamino-1,3,4-thiadiazolium-2-thiolates by using omega-bromo-omega-(1H-1,2,4-triazol-1-yl)acetophenone as catalyst, J CHIN CHEM, 47(4B), 2000, pp. 943-946
Synthesis and antibacterial activity of s-triazoles, s-triazolo[3,4-b]-1,3,4-thiadiazines and s-triazolo[3,4-b]-1,3,4-thiadiazoles of 5-methylisoxazole
Authors: Hui, XP Zhang, LM Zhang, ZY Wang, Q Wang, F
Citation: Xp. Hui et al., Synthesis and antibacterial activity of s-triazoles, s-triazolo[3,4-b]-1,3,4-thiadiazines and s-triazolo[3,4-b]-1,3,4-thiadiazoles of 5-methylisoxazole, J CHIN CHEM, 47(3), 2000, pp. 535-539
Synthesis and antibacterial activities of 1,3,4-thiadiazole, 1,3,4-oxadiazole and 1,2,4-triazole derivatives of 5-methylisoxazole
Authors: Hui, XP Zhang, LM Zhang, ZY Wang, Q Wang, F
Citation: Xp. Hui et al., Synthesis and antibacterial activities of 1,3,4-thiadiazole, 1,3,4-oxadiazole and 1,2,4-triazole derivatives of 5-methylisoxazole, I J CHEM B, 38(9), 1999, pp. 1066-1069
Studies on semisynthesis and antibacterial activity of 3-heterocyclicthiomethyl cephalosporins
Authors: Hao, L Hui, XP Zhang, ZY Guan, ZW He, YL Yu, HJ
Citation: L. Hao et al., Studies on semisynthesis and antibacterial activity of 3-heterocyclicthiomethyl cephalosporins, CHEM J CH U, 20(10), 1999, pp. 1564-1569
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