L
Liping Wang
Researcher at Jiangxi Science and Technology Normal University
Publications - 28
Citations - 53
Liping Wang is an academic researcher from Jiangxi Science and Technology Normal University. The author has contributed to research in topics: Total synthesis & Aldol reaction. The author has an hindex of 4, co-authored 28 publications receiving 41 citations.
Papers
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Journal ArticleDOI
An Efficient Method for the Production of Cyclohexylamine from Cyclohexanone and Ammonia over Cu-Cr-La/γ-Al2O3
Shuanglin Qin,Pan Wang,Huang Shuangping,Liu Shuai,Wang Gaopeng,Liping Wang,Sun Meng,Wang Xiaoji +7 more
TL;DR: In this paper, the reductive amination of cyclohexanone with ammonia over Cu-Cr-La/γ-Al2O3 was investigated and it was found that a proper solvent with high solubility of ammonia and 4A molecular sieves for the elimination of generated water contributed to cyclohexylamine formation in the premixing process.
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A dual-functional urea-linked conjugated porous polymer anchoring silver nanoparticles for highly efficient CO2 conversion under mild conditions.
Xiaoji Wang,Xiaoji Wang,Li Wang,Wang Jianxin,Jie Zhu,Yuting Li,Xiaozhen Liu,Liping Wang,Li Lin +8 more
TL;DR: The resulting Ag@UCPP as a heterogeneous catalyst exhibited excellent activity for the carboxylative cyclization of propargyl alcohols with CO2 under mild conditions, together with good recyclability, probably attributed to the synergistic effect of the UCPP on the adsorption and activation of CO2 and the immobilization of Ag nanoparticles.
Journal ArticleDOI
A total synthesis of (+)-brazilin
Shuangping Huang,Wentao Ou,Li Wang,Hesheng Xiao,Yiying Pang,Yi Zhou,Xiaoji Wang,Xihua Yang,Liping Wang +8 more
TL;DR: In this article, a concise total synthesis of (+)-brazilin from readily available 4-bromo-1,2-dimethoxybenzene was described, where a Sharpless asymmetric dihydroxylation was employed to introduce the chiral hydroxyl group and trifluoroacetic acid (TFA) catalyzed one-pot intramolecular tandem Prins/Friedel-Crafts reaction was also involved as the key transformation in the construction of the hybrid chromane and indane framework.
Journal ArticleDOI
Concise Total Synthesis of Ieodomycin A and B
TL;DR: A concise total synthesis of ieodomycin A and B was achieved in six and seven steps respectively from commercially available geraniol, which involved the construction of the C-5 hydroxyl via an Ti(OiPr)4/(S)-BINOL-mediated asymmetric aldol reaction as the key step as mentioned in this paper.
Patent
Method for stereoselective synthesis of IeodomycinA and B
TL;DR: In this paper, a method for asymmetric synthesis of chain nonsaturated ester IeodomycinA and B was proposed, which utilizes geraniol as a raw material and utilizes Swern oxidation, 3-chloroperbenzoic acid epoxidation reaction, Wittig reaction and periodic acid oxidation cutting-off reaction.