A5024064895- Chemical synthesis and alkaloids
- Cyclopropane Reaction Mechanisms
- Catalytic C–H Functionalization Methods
- Crystallization and Solubility Studies
- TiO2 Photocatalysis and Solar Cells
- Asymmetric Synthesis and Catalysis
- X-ray Diffraction in Crystallography
- Gas Sensing Nanomaterials and Sensors
- Traditional Chinese Medicine Analysis
- Mathematical Analysis and Transform Methods
- Advanced Mathematical Physics Problems
- Natural product bioactivities and synthesis
- Transition Metal Oxide Nanomaterials
- Synthesis of Organic Compounds
- Phytochemistry and Biological Activities
- Phenothiazines and Benzothiazines Synthesis and Activities
- Electrospun Nanofibers in Biomedical Applications
- Traditional Chinese Medicine Studies
- Synthesis and Reactions of Organic Compounds
- Advanced Photocatalysis Techniques
- Metabolomics and Mass Spectrometry Studies
- Chromatography in Natural Products
- Polysaccharides Composition and Applications
- biodegradable polymer synthesis and properties
- Synthesis and Catalytic Reactions
Shenyang Pharmaceutical University
2014-2022
Chaohu University
2021
Jilin Medical University
2020
Soochow University
2014-2017
Bohai University
2014
Abstract NiCo 2 O 4 nanostructures were directly grown on fluorine‐doped tin oxide (FTO) conductive substrates by using a facile, low‐temperature hydrothermal process and their morphology was precisely adjusted from nanowires (NW) to nanosheets (NS) novel nanowire‐woven nanosheet (NW–NS) arrays. Such then explored for photoelectrodes of p‐type dye‐sensitized solar cells (DSSCs), in which the conversion efficiency demonstrated strong dependence morphology. NW–NS based p‐DSSCs showed high...
Abstract In the present investigation, incorporation of oxepine ring into a polycyclic-fused quinoline system leading to series structurally novel hybrids benzo[ h ]areno[6,7]oxepino[3,4- b ]quinolin-8(14 H )-ones has been achieved through simple, and economical two-step procedure that involves one-pot synthesis 2-(aryloxymethyl)benzo[ ]quinoline-3-carboxylic acids followed by intramolecular Friedel-Crafts acylation reaction using Eaton’s reagent.
A facile synthesis of a series new 5-bromotropono[c]pyrazole derivatives (3 and 10--15) as well 5-bromotropono[c]isoxazole (17) is described, involving condensation reaction 3-acetyl-5-bromotropolone (1) with hydrazine monohydrate (2), arylhydrazine hydrochlorides (4--9), hydroxylamine hydrochloride (16), respectively. All the synthesized compounds were obtained in good yields 56%--77% their structures characterized by spectral data HRMS.
Abstract Curcumin (Cur) is a natural anticancer pigment, but its poor absorption and extensive metabolism limit clinical applications. In this study, an ultra‐high performance liquid chromatography/quadrupole time‐of‐flight mass spectrometry method was employed to investigate the metabolic profiles of Cur self‐emulsifying drug delivery system (C‐SEDDS) in rat plasma, urine, bile feces after oral administration at 100 mg/kg. Protein precipitation, solid‐phase ultrasonic extractions were used...
Abstract An approach to hydrocarbazoles bearing an all‐carbon quaternary center at C4a position was developed via a Brønsted acid‐initiated Diels‐Alder cycloaddition/retro‐aza‐Michael addition cascade process from azepino[4,5‐ b ]indoles and commercially available dienophiles. The method provided range of in 63–99% yields. practicality this transformation demonstrated by scale‐up experiment various transformations several hydrocarbazole derivatives the tetracyclic indoline scaffold....
A unique approach to hydrocarbazoles bearing an all-carbon quaternary center at C4a position was developed via a Brønsted acid-initiated Diels-Alder cycloaddition/retro-Michael addition cascade process from facilely prepared azepino[4,5-b]indoles and commercially available acrolein. The method provided range of in good excellent yields. practi-cality this transformation demonstrated by scale-up experiment various transformations several hydrocarbazole derivatives.
Abstract We study the boundedness of oscillatory integral <m:math xmlns:m="http://www.w3.org/1998/Math/MathML" display="block"> <m:msub> <m:mrow> <m:mi>T</m:mi> </m:mrow> <m:mi>α</m:mi> <m:mo>,</m:mo> <m:mi>β</m:mi> </m:msub> <m:mi>f</m:mi> <m:mo>(</m:mo> <m:mi>x</m:mi> <m:mi>y</m:mi> <m:mo>)</m:mo> <m:mo>=</m:mo> <m:munder> <m:mo>∫</m:mo> <m:msup> <m:mi>Q</m:mi> <m:mn>2</m:mn> </m:msup> </m:munder> <m:mo>−</m:mo> <m:mi>γ</m:mi> <m:mn>1</m:mn> <m:mi>t</m:mi> <m:mi>s</m:mi> <m:mi>e</m:mi>...
A unique approach to hydrocarbazoles bearing an all-carbon quaternary center at C4a position was developed via a Brønsted acid-initiated Diels-Alder cycloaddition/retro-Michael addition cascade process from facilely prepared azepino[4,5-b]indoles and commercially available acrolein. The method provided range of in good excellent yields. practi-cality this transformation demonstrated by scale-up experiment various transformations several hydrocarbazole derivatives.