Wei Li
Shandong University
25 Papers
79 Citations
Wei Li is an academic researcher from Shandong University. The author has contributed to research in topics: Chemistry & Medicine. The author has an hindex of 9, co-authored 18 publications. Previous affiliations of Wei Li include Shandong University of Traditional Chinese Medicine.
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Papers
TBHP/TFA mediated oxidative cross-dehydrogenative coupling of N-heterocycles with aldehydes.
TL;DR: An effective and metal-free oxidative cross-dehydrogenative coupling of N-heterocycles with diverse aldehydes and C1-acyl substituted heterocycles has been established in the presence of TBHP/TFA.
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Tetramic Acids and Pyridone Alkaloids from the Endolichenic Fungus Tolypocladium cylindrosporum
Xiao-Bin Li,Lin Li,Rong-Xiu Zhu,Wei Li,Wenqiang Chang,Lu-Lu Zhang,Xiao-Ning Wang,Zun-Tian Zhao,Hong-Xiang Lou +8 more
TL;DR: Bioassay of the isolated compounds found that pyridoxatin was cytotoxic to human cancer cells by induction of G0/G1 cell cycle arrest and apoptosis, and structures of these compounds were determined by comprehensive analysis of spectroscopic data and single-crystal X-ray diffraction determination.
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Salinity, temperature and pressure effect on hydrogen wettability of carbonate rocks
TL;DR: In this paper , the authors studied the carbonate rock wettability alteration when exposed to the hydrogen environments, and they explored the salinity, temperature and pressure effect on H2/carbonate rock/brine wetability.
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p-Terphenyl Derivatives from the Endolichenic Fungus Floricola striata.
Wei Li,Wei Gao,Ming Zhang,Yue-Lan Li,Lin Li,Xiao-Bin Li,Wenqiang Chang,Zun-Tian Zhao,Hong-Xiang Lou +8 more
TL;DR: Evaluation of the isolated compounds against Candida albicans revealed that the most active compound, 3 (MIC 8 μg/mL), exerted fungicidal action by destruction of the cell membrane.
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Indium-catalyzed oxidative cross-dehydrogenative coupling of chromenes with 1,3-dicarbonyls and aryl rings
TL;DR: An effective indium-catalyzed oxidative cross-dehydrogenative coupling of electronically varied chromenes with 1,3-dicarbonyl compounds and aryl rings has been established and both the C-H alkylation and aRYlation proceed smoothly at room temperature to afford diverse α-substituted chromene compounds in up to 91% yields.
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