A series of novel pyrazoles compounds were synthesized by the reaction of five kinds of substitute α-bromoacetophenone with pyrazole intermediates which was prepared by the reaction of chalcones and thiosemicarbazones. This method has some advantages such as mild reaction condition, easy operation and higher yield. All the compounds were confirmed by elemental analysis, IR and 1H NMR.
Jianzhong ZhangZhengfeng XieRanran WangFangming Liu
Schiff base-Cu（II） complex is found to be an effective catalyst for the condensation reaction of indole with aldehydes using ethanol as the solvent. The characterization of the catalysts was carried out using XRD and FT-IR.
Yong Lei YangNing Ning WanWen Ping WangZheng Feng XieJi De Wang
Friedel-Crafts alkylation of indoles with nitroalkenes catalyzed by a novel Zn（II）-thiourea complex has been developed. The remarkable advantages of this reaction are mild reaction conditions, simple workup procedure, high yield of products and the use of ethanol as acceptable solvent.
An efficient enantioselective Michael addition of ethyl-2-cyanoacetate and diethyl malonate to α,β-unsaturated ketones catalyzed by a simple chiral Schiff base, and products were obtained in good yields at room temperature.
A series of new ligands L_1-L_7 were readily prepared in one step.Friedel-Crafts alkylation of indoles with nitroalkenes catalyzed by a novel Cu（Ⅱ）-L complex has been developed.The remarkable advantages of this reaction are mild reaction conditions,simple workup procedure,high yields of products and the use of ethanol as a green solvent.
Ning Ning WanYong Lei YangWen Ping WangZheng Feng XieJi De Wang
A series of novel Schiff bases bearing triazole structure were synthesized and characterized by LR and NMR. Mn（OAc）2/Schiff base efficiently catalyzed Henry reaction of nitroalkanes with aldehydes to produce the corresponding products of ^-nitroalcohols, under mild conditions with high yields （up to 99%）. A reaction mechanism is proposed based on the experimental results.
Guang Peng Zhou Yong Hai Hui Ning Ning Wan Qiu Ju Liu Zheng Feng Xie Ji De Wang
Co（ClO_4））_2·6H_2O/bis-Schiff base complexes promoted the conjugate addition of indole toα,β-unsaturated ketones under mild conditions,giving the corresponding addition products with high yields.And the complex has been characterized with XRD and IR.
CrCl3·6H2O/hydrogenated bis-Schiff base is found to be an effective catalyst system for synthesis of bis（indoly） methane via electrophilic addition reaction of indoles with aldehydes using acetonitrile as the solvent. The yields of isolated products are from good to excellent.
