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Long Lu

Researcher at Chinese Academy of Sciences

Publications -  128
Citations -  3562

Long Lu is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Trifluoromethyl & Catalysis. The author has an hindex of 29, co-authored 128 publications receiving 3134 citations. Previous affiliations of Long Lu include University of Science and Technology of China & Yangzhou University.

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An Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation

TL;DR: The authors gratefully acknowledge financial support from theNational Basic Research Program of China (2012CB821600, 2010CB126103), the Key Program of Natural Science Foundation ofChina (21032006), the National Natural Science foundation ofChina, Agro-scientific Research inthe Public Interest, the National Key TechnologiesR&D Program (2011BAE06B05), the Shanghai Scientific ResearchProgram (10XD1405200), and SIOC for financial support.
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Shelf-stable electrophilic reagents for trifluoromethylthiolation.

TL;DR: Two different types of electrophilic trifluoromethylthiolating reagents are discovered, which are more reliable in transition-metal-Catalyzed reactions such as copper-catalyzed trif LU/vinyl/alkylboronic acids and silver-catalystzed decarboxylative trifLUorometHylthio group into small molecules and aliphatic carboxylic acids as well as in the organocatalytic asymmetric
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Effects of 5-aminolevulinic acid on oilseed rape seedling growth under herbicide toxicity stress

TL;DR: AlA has promotive effects in the recovery of growth and development of rape seedlings under herbicide ZJ0273 toxicity stress, and it is found that plants treated with 1 mg/L ALA produced the highest shoot fresh weights, shoot lengths, rootfresh weights, and root oxidizability when the seeds were treated with different concentrations of ZJ 0273.
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Silver-catalyzed decarboxylative trifluoromethylthiolation of aliphatic carboxylic acids in aqueous emulsion.

TL;DR: It was proposed that the radical, generated from the silver-catalyzed decarboxylation in the "oil-in-water" droplets, could easily react with the trifluoromethylthiolating reagent to form the product.
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N-Trifluoromethylthio-dibenzenesulfonimide: A Shelf-Stable, Broadly Applicable Electrophilic Trifluoromethylthiolating Reagent.

TL;DR: The super electrophilicity of a shelf-stable, easily prepared trifluoromethylthio-dibenzenesulfonimide 7 was demonstrated and exhibits reactivity remarkably higher than that of other known electrophilic trifLUorometHylthiolating reagents.