20 results on '"Xile, Hu"'
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2. Z‑Selective Synthesis of Vinyl Boronates through Fe-Catalyzed Alkyl Radical Addition.
3. Transition Metal Oxides as Electrocatalysts for the Oxygen Evolution Reaction in Alkaline Solutions: An Application-Inspired Renaissance.
4. Oxidatively Electrodeposited Thin-Film Transition Metal (Oxy)hydroxides as Oxygen Evolution Catalysts.
5. γ-Selective Allylation of (E)-Alkenylzinc Iodides Prepared by Reductive Coupling of Arylacetylenes with Alkyl Iodides.
6. Alkoxy Hydrosilanes As Surrogates of Gaseous Silanes for Hydrosilylation of Alkenes.
7. A Functional Model of [Fe]-Hydrogenase.
8. Synthesis of E-Alkyl Alkenesfrom Terminal Alkynes via Ni-Catalyzed Cross-Coupling of Alkyl Halideswith B-Alkenyl-9-borabicyclo[3.3.1]nonanes.
9. An Optically Transparent Iron Nickel Oxide Catalyst for Solar Water Splitting.
10. Solar Hydrogen Production by Amorphous Silicon Photocathodes Coated with a Magnetron Sputter Deposited Mo2C Catalyst.
11. Chemoselective Hydrogenation and Transfer Hydrogenation of Aldehydes Catalyzed by Iron(II) PONOP Pincer Complexes.
12. Z-Selective Olefin Synthesis via Iron-Catalyzed Reductive Coupling of Alkyl Halides with Terminal Arylalkynes.
13. Evidence from in Situ X-ray Absorption Spectroscopy for the Involvement of Terminal Disulfide in the Reduction of Protons by an Amorphous Molybdenum Sulfide Electrocatalyst.
14. A Monometallic Iron(I) Organoferrate.
15. Ultrathin Cobalt-Manganese Layered Double Hydroxide Is an Efficient Oxygen Evolution Catalyst.
16. Bimetallic Oxidative Addition Involving Radical Intermediates in Nickel-Catalyzed Alkyl–Alkyl Kumada Coupling Reactions.
17. Synthesis and Characterization of a Series of Model Complexes of the Active Site of [Fe]-Hydrogenase (Hmd).
18. A Structure-Activity Study of Ni-Catalyzed Alkyl-Alkyl Kumada Coupling, Improved Catalysts for Coupling of Secondary Alkyl Halides.
19. Why Are (NN2)Ni Pincer Complexes Active for Alkyl−Alkyl Coupling: β-H Elimination Is Kinetically Accessible but Thermodynamically Uphill.
20. Carbon Dioxide as the C1 Source for Direct C−H Functionalization of Aromatic Heterocycles.
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