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Zhihai Ke

Researcher at The Chinese University of Hong Kong

Publications -  42
Citations -  1018

Zhihai Ke is an academic researcher from The Chinese University of Hong Kong. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 17, co-authored 35 publications receiving 793 citations. Previous affiliations of Zhihai Ke include Sun Yat-sen University & National University of Singapore.

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Catalytic asymmetric bromoetherification and desymmetrization of olefinic 1,3-diols with C2-symmetric sulfides.

TL;DR: An enantioselective and highly diastereoselectives bromoetherification and desymmetrization of olefinic 1,3-diols has been developed using a C2-symmetric cyclic sulfide catalyst and successfully applied to the synthesis of the key intermediate of an orally active antifungal drug posaconazole (Noxafil).
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A Platinum(II) Terpyridine Metallogel with an L‐Valine‐Modified Alkynyl Ligand: Interplay of Pt⋅⋅⋅Pt, π–π and Hydrogen‐Bonding Interactions

TL;DR: A series of platinum(II) terpyridine complexes with L-valine-modified alkynyl ligands has been synthesized and is shown to be capable of gel formation, which is in sharp contrast to the gelation properties of the corresponding organic counterparts.
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Design, synthesis and crystallographic analysis of nitrile-based broad-spectrum peptidomimetic inhibitors for coronavirus 3C-like proteases.

TL;DR: It is shown that the nitrile-based peptidomimetic inhibitors are effective against 3CLpro, and they inhibit 3CL Pro from a broad range of coronaviruses.
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Electrochemical self-assembly of ZnO nanoporous structures

TL;DR: In this article, ZnO nanoporous structures were prepared on Cu substrates by electrochemical deposition in solutions of ZnCl2 + ethylenediaminetetraacetic acid (EDTA) at a temperature of 90 °C.
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Conformational and supramolecular properties of main chain and cyclic click oligotriazoles and polytriazoles.

TL;DR: It is believed that many new and unique conformational and supramolecular properties can be created by incorporating the correct type of functional group partners into the oligo- and polytriazole backbone.