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Yu Lan

Researcher at Zhengzhou University

Publications -  350
Citations -  10789

Yu Lan is an academic researcher from Zhengzhou University. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 46, co-authored 288 publications receiving 7583 citations. Previous affiliations of Yu Lan include Wuhan University & Chinese Academy of Sciences.

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Visible‐Light‐Mediated Decarboxylation/Oxidative Amidation of α‐Keto Acids with Amines under Mild Reaction Conditions Using O2

TL;DR: A novel, simple, and efficient radical oxidative decarboxylative coupling with the assistant of the photocatalyst [Ru(phen)3 ]Cl2 is described, and various functional groups are well-tolerated in this reaction and thus provides a new approach to developing advanced methods for aerobic oxidative decarations.
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Rhodium-catalyzed C-H activation of phenacyl ammonium salts assisted by an oxidizing C-N bond: a combination of experimental and theoretical studies.

TL;DR: In this article, α-ammonium acetophenones with an oxidizing C-N bond have been designed as substrates for Rh(III)-catalyzed C-H activation under redox-neutral conditions.
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Chemoselective Carbophilic Addition of α-Diazoesters through Ligand-Controlled Gold Catalysis†

TL;DR: The chemoselective addition of arenes and 1,3-diketones to α-aryldiazoesters was achieved through ligand-controlled gold catalysis, representing a new and efficient approach to form "carbophilic carbocations", which selectively react with carbon nucleophiles.
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Mechanistic view of Ru-catalyzed C–H bond activation and functionalization: computational advances

TL;DR: The mechanisms of Ru-catalyzed arylation, alkylation, and alkenylation of arenes are summarized, and these transformations can be categorized into cross-coupling with electrophiles or oxidative coupling with nucleophiles.
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Nine-Membered Benzofuran-Fused Heterocycles: Enantioselective Synthesis by Pd-Catalysis and Rearrangement via Transannular Bond Formation

TL;DR: The first enantioselective formal [5+4] cycloaddition is realized under palladium catalysis to deliver benzofuran-fused nine-membered rings in excellent efficiency and stereoselectivity.