研究领域
目前主要从事除草剂、杀菌剂等生物活性物质的设计、合成、活性及构效关系研究。
近期论文
1. Feng Liu, Meiyan Wang, Xinhuan Teng, Peizhi Zhang, Lin Jiang*. Synthesis and biological evaluation of novel 2-(substituted isoxazol-4-yl)-5-arylamino-1,3,4- oxadiazoles. Res Chem Intermed, 2014, 40:1575–1581
2. Shaofang Zhou, Fubo Li, Peizhi Zhang, Lin Jiang*. Synthesis and antifungal activity of novel 1-(1H-benzoimidazol-1-yl)propan-2-one oxime-ethers containing the morpholine moiety. Res Chem Intermed. 2013, 39: 1735–1743.
3. Zeyuan ZHANG, Wei MU, Zengchen JI, Lin JIANG*. Synthesis and antifungal activity of novel 2,5-disubstituted-1,3,4- oxadiazoles containing benzimidazole moiety. J. Pestic. Sci. 2012, 37: 338-341.
4. Pei Zhi Zhang, Shao Fang Zhou, Tian Ren Li, Lin Jiang*. Efficient synthesis and in vitro antifungal activity of 1H-benzimidazol-1-yl acetates/propionates containing 1H-1,2,4-triazole moiety. Chin. Chem. Lett. 2012, 23: 1381-1384.
5. Maorong WANG, Linying SUN, Fuxian WAN, Lin JIANG*. Synthesis and Phytotoxic Activity of Novel Acylthiourea and 2H-1,2,4-Thiadiazolo[2,3-a] pyrimidine Derivatives. J. Pestic. Sci. 2012, 37: 15-19.
6. Lin Jiang*, Peng Cao, Yulei Zhang, Xiezhong Xie. Structure and spectral property of 8-(2-(5-(4-methylphenyl) -2-thienyl)vinyl)-10,10-dimethyl-10H-pyrido[1,2-a]indolium perchlorate. Res Chem Intermed. 2012, 38:2229-2235.
7. Mao Rong Wang, Lin Jiang*, Shao Fang Zhou, Ze Yuan Zhang, Zeng Chen Ji. Ultrasound-assisted synthesis and preliminary bioactivity of novel 2H-1,2,4-thiadiazolo[2,3-a] pyrimidine derivatives containing fluorine. Chin. J. Chem. Lett. 2012, 23, 557-560.
8. Jiang Lin*, Wang Haibo, Mu Wei, Ji, Zengchen, Cao, Peng. Synthesis and Fungicidal Activity of 2-Acetyl-6-(un)substituted- 1H-benzimidazole Oxime-ethers. Chin. J. Chem., 2011, 29, 539-543.
9. Lin Jiang*, Hao Wang, Mao-Rong Wang, Xin-Huan Teng. Synthesis and biological activity of4-(4,6-disubstitutedpyrimidin-2-yloxy) phenoxy acetates. Molecules, 2010, 15, 1074-1081.
10. Lin JIANG,* Feng LIU, Dengke ZHANG, Haibo WANG.Synthesis and antifungal activity of 1-substitutedphenyl-3-(5- halobenzimidazol-2-yl) acylurea. J. Pestic. Sci, 2010, 35(1): 33-35.