22198-19-2Relevant academic research and scientific papers
Synthesis of Imidazoles and Oxazoles via a Palladium-Catalyzed Decarboxylative Addition/Cyclization Reaction Sequence of Aromatic Carboxylic Acids with Functionalized Aliphatic Nitriles
Dai, Ling,Yu, Shuling,Lv, Ningning,Ye, Xuanzeng,Shao, Yinlin,Chen, Zhongyan,Chen, Jiuxi
supporting information, p. 5664 - 5668 (2021/08/01)
We herein report an efficient approach for the assembly of multiply substituted imidazoles and oxazoles in a single-step manner. These transformations are based on a decarboxylation addition and annulation of readily accessible aromatic carboxylic acids a
Nickel-Catalyzed Construction of 2,4-Disubstituted Imidazoles via C–C Coupling and C?N Condensation Cascade Reactions
Fang, Shengyang,Yu, Haihua,Yang, Xicheng,Li, Jianqi,Shao, Liming
supporting information, p. 3312 - 3317 (2019/06/13)
A convenient Ni(II)-catalyzed C?C and C?N cascade coupling reaction was developed to directly access various 2,4-disubstituted imidazoles. The reaction scope covers a variety of aryl and aliphatic substitutions, which demonstrate moderate-to-excellent yie
ACETONITRILE DERIVATIVE, PEST CONTROL AGENT, AND METHOD OF USING THE SAME
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Page/Page column 85-86, (2010/11/08)
An acetonitrile derivative represented by the general formula (I): (I) (wherein A represents (VV) or (WW) B represents (XX) (YY) or (ZZ) and R represents hydrogen, C1-6 alkyl, etc. (Q1, Q2, Ar1, and Ar2 each represents phenyl, substituted phenyl, etc.; R1, R2, R3, R4, R6, R7, and R8 each represents hydrogen, C1-6 alkyl, etc.; R5 represents C1-6 alkyl, etc.; G represents NR10, etc.; W represents O, S, NR9, etc.; R9 and R10 each represents hydrogen, etc.; and n is an integer of 0-4)). The acetonitrile derivative is remarkably active in controlling pests even when used in a small dose. It is useful as an agricultural or horticultural bactericide or an animal parasite control agent.
