414 results on '"Zhu, Xiao-Qing"'
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2. Formation mechanisms and geological significance of the Lower Triassic fine-grained mixed sedimentary rocks in the Central Uplift of the South Yellow Sea Basin, eastern China
3. Re-vitrectomy for recurrent retinal detachment in post-vitrectomy eyes of rhegmatogenous retinal detachment
4. Structural characteristics of the Chiwei Platform and their implications for the back-arc rifting of the Okinawa Trough, East China Sea
5. The synthesis of furoquinolinedione and isoxazoloquinolinedione derivatives as selective Tyrosyl-DNA phosphodiesterase 2 (TDP2) inhibitors
6. Establishing the Thermodynamic Cards of Dipine Models' Oxidative Metabolism on 21 Potential Elementary Steps.
7. A wrapped time-frequency combined selection in the source domain
8. Thermodynamic evaluations of the acceptorless dehydrogenation and hydrogenation of pre-aromatic and aromatic N-heterocycles in acetonitrile
9. Molecular Characterization, Expression and Binding Specificity Analysis of the Odorant-Binding Proteins of Scleroderma sichuanensis Xiao (Hymenoptera: Bethylidae)
10. Construction of an Indoor Topological Map of a Robot Based on Prunable Self-Organizing Map
11. Discovery of Late Devonian plants from the southern Yellow Sea borehole of China and its palaeogeographical implications
12. Mesozoic–Cenozoic denudation and thermal history in the Central Uplift of the South Yellow Sea basin and the implications for hydrocarbon systems: Constraints from the CSDP-2 borehole
13. Evaluation of Organic Hydride/Acid Pairs as a Type of Thermodynamic-Potential-Regulated Multisite Proton-Coupled Electron Transfer Reagents.
14. A new method for determining the intrinsic resistance energy of H‐atom transfer reaction and structure–activity relationship of H‐donating ability
15. Effect of N, S atoms on the mechanisms of H‐transfer for five‐membered nitrogen‐containing heterocycles
16. Geology and geochemistry of the Xiaoshanba bauxite deposit, Central Guizhou Province, SW China: Implications for the behavior of trace and rare earth elements
17. Thermodynamic Evaluations of Amines as Hydrides or Two Hydrogen Ions Reductants and Imines as Protons or Two Hydrogen Ions Acceptors, as Well as Their Application in Hydrogenation Reactions
18. Structure–activity relationship of alkanes and alkane derivatives for the abilities of C(sp3)H bonds toward their H‐atom transfer reactions
19. A new method for determining the intrinsic resistance energy of H‐atom transfer reaction and structure–activity relationship of H‐donating ability.
20. Effect of N, S atoms on the mechanisms of H‐transfer for five‐membered nitrogen‐containing heterocycles.
21. Paracercopis Schmidt 1925
22. The Oriental spittlebug genus Paracercopis Schmidt (Hemiptera: Cercopoidea: Cercopidae) revisited, with description of one new species from Hubei, China
23. Paracercopis unicolor Liang, Zhang & Xiao 2023, new species
24. Selenylation modification: enhancement of the antioxidant activity of a Glycyrrhiza uralensis polysaccharide
25. A Mechanism Study of Redox Reactions of the Ruthenium-oxo-polypyridyl Complex
26. Greater Invasion and Persistence of mcr-1- Bearing Plasmids in Escherichia coli than in Klebsiella pneumoniae
27. Characteristic Activity Parameters of Electron Donors and Electron Acceptors
28. Thermodynamics Evaluation of Selective Hydride Reduction for α,β-Unsaturated Carbonyl Compounds
29. Thermodynamic and Kinetic Studies of the Activities of Aldehydic C−H Bonds toward Their H‐Atom Transfer Reactions
30. Effect of Glycyrrhiza uralensis Fisch polysaccharide on growth performance and immunologic function in mice in Ural City, Xinjiang
31. Structure–activity relationship of alkanes and alkane derivatives for the abilities of C(sp3)H bonds toward their H‐atom transfer reactions.
32. Quantitative evaluation of the actual hydrogen atom donating activities of O–H bonds in phenols: structure–activity relationship
33. Enhancing ergosterol production in Pichia pastoris GS115 by overexpressing squalene synthase gene from Glycyrrhiza uralensis
34. Thermodynamic Evaluation on Alkoxyamines of TEMPO Derivatives, Stable Alkoxyamines or Potential Radical Donors?
35. Wind suitability in site analysis of coastal concave terrains using computational fluid dynamics simulation: a case study in East Asia
36. Comparison of Thermodynamic Energies for Elementary Steps of Anionic Hydrides to Release Hydride Ions in Acetonitrile
37. Comparison of the Hydride-Donating Ability and Activity of Five- and Six-Membered Benzoheterocyclic Compounds in Acetonitrile
38. Quantitative Evaluation of the Hydrogen‐Donating Abilities ofAmines and Amides in Acetonitrile
39. Protolith reconstruction and geochemical study on the wall rocks of Anshan BIFs, Northeast China: Implications for the provenance and tectonic setting
40. Effects of Senegenin against hypoxia/reoxygenation-induced injury in PC12 cells
41. Comparison between 1,2-Dihydropyridine and 1,4-Dihydropyridine on Hydride-Donating Ability and Activity
42. Kinetic Studies of Hantzsch Ester and Dihydrogen Donors Releasing Two Hydrogen Atoms in Acetonitrile
43. New Insights into the Actual H-Abstraction Activities of Important Oxygen and Nitrogen Free Radicals: Thermodynamics and Kinetics in Acetonitrile
44. Discovering and Evaluating the Reducing Abilities of Polar Alkanes and Related Family Members as Organic Reductants Using Thermodynamics
45. Study on in vitro and in vivo antibacterial effect and antibacterial mechanism of selenide Glycyrrhiza polysaccharide combined with antibiotics against Proteus mirabilis.
46. Quantitative evaluation of H-donating abilities of C(sp3)–H bonds of nitrogen-containing heterocycles in hydrogen atom transfer reaction.
47. Quantitative comparison of the actual antioxidant activity of Vitamin C, Vitamin E, and NADH
48. Thermodynamics of the elementary steps of organic hydride chemistry determined in acetonitrile and their applications
49. Evaluation and comparison of antioxidant abilities of five bioactive molecules with C–H and O–H bonds in thermodynamics and kinetics
50. Thermodynamics regulated organic hydride/acid pairs as novel organic hydrogen reductants
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