Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Quan-Zhe Li"'
Publikováno v:
Molecules, Vol 28, Iss 17, p 6193 (2023)
Natural products play a key role in innovative drug discovery. To explore the potential application of natural products and their analogues in pharmacology, total synthesis is a key tool that provides natural product candidates and synthetic analogue
Externí odkaz:
https://doaj.org/article/1ba33e37b14c4624876034492bcaf854
Publikováno v:
Chem Catalysis. 2:3185-3195
Autor:
Quan‐Zhe Li, Si‐Hua Hou, Jun‐Chen Kang, Peng‐Fei Lian, Yu Hao, Chao Chen, Jia Zhou, Tong‐Mei Ding, Shu‐Yu Zhang
Publikováno v:
Angewandte Chemie. 134
Publikováno v:
Pattern Recognition Letters. 139:128-138
Biomedical and inertial sensors can be used to generate a complete view of complicated physiological changes in a continuous, real-time, and non-invasive manner. As inappropriate on-body attachments may result in errors, the localization information
Autor:
Quan-Zhe Li, Shu-Yu Zhang, Xun-Hui Wang, Jia Zhou, Peng-Fei Lian, Wei Jiang, Fu-Xin Tan, Chao Chen, Yu Hao, Guo-Dong Zhu
Publikováno v:
Organic Letters. 22:2448-2453
We have developed a novel π-π interaction and dual H-bond concerted control strategy to construct axially chiral naphthylamine heterocycles. With ortho-alkynyl-naphthylamines as the electrophile, indoles and 4-hydroxycoumarins were efficiently empl
Autor:
Si-Hua Hou, He-Yuan Bai, Xun-Hui Wang, Yan-Yan Ma, Quan-Zhe Li, Tong-Mei Ding, Shu-Yu Zhang, Deng-Gao Zhao
Publikováno v:
Synthesis. 51:2697-2704
A simple and efficient protocol for para-selective C–H amination of 1-naphthylamide derivatives under silver catalysis is described. This reaction system could proceed without the help of directing group and a broad range of substrates were proved
Autor:
Zhi-Qiang Yan, Jin-Long Pan, Tong-Mei Ding, Chao Chen, Quan-Zhe Li, Wei Jiang, Guo-Dong Zhu, Tuan-Qing Liu
Publikováno v:
Organic & Biomolecular Chemistry. 17:8589-8600
Herein, a cascade [3 + 2] annulation of N-aryloxyacetamides with 3-(hetero)arylpropiolic acids affording benzofuran-2(3H)-ones via rhodium(iii)-catalyzed redox-neutral C-H functionalization/isomerization/lactonization using an internal oxidative dire
Publikováno v:
Organicbiomolecular chemistry. 18(37)
We have developed a new synthetic methodology for the rapid construction of cyclopenta[b]naphthalene frameworks from the reaction of propargylic alcohol tethered methylenecyclopropanes with mesyl chloride in the presence of triethylamine through casc
Publikováno v:
International Journal of Knowledge Engineering. 2:182-186