Microwave Assisted Synthesis, Antifungal Activity, and DFT Study of Some Novel Triazolinone Derivatives

Table 1

The antifungal activity of title compounds in vivo at 500 ppm (%).

Number	Phytophthora infestans	Botrytis cinerea	Corynespora cassiicola	Rhizoctonia solani	Pythium ultimum
5a	25.66	−37.95	19.81	0	44.44
5b	−0.8	−61.1	68.6	3.33	−11.11
5c	−0.8	−61.1	73.93	0	77.78
5d	−0.8	−49.52	26.26	0	11.11
5e	−0.8	−38.91	13.08	0	−88.89
5f	−0.8	−51.45	18.13	33.89	88.89
5g	−0.8	−56.28	9.72	2.22	33.33
5h	−0.8	−52.42	6.36	29.44	66.67
5i	−0.8	−38.91	37.76	0	44.44
5j	−0.8	−48.56	39.44	0	−11.11
5k	−0.8	−33.12	34.95	0	−22.22
5l	29.16	−27.34	37.76	0	−22.22
5m	−0.8	−7.08	24.86	0	33.33
5n	−0.8	−42.77	0.19	11.11	33.33
5o	−0.8	−20.58	4.11	0	11.11
Dimethomorph	97.76
Fludioxonil		86.98
Chlorothalonil			45.89
Validamycin				62.50
Zhongshengmycin					0