Guangkuo Zeng

ORCID: 0000-0003-3452-7890
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About
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Research Areas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Catalytic C–H Functionalization Methods
  • Chemical Synthesis and Analysis
  • Asymmetric Hydrogenation and Catalysis
  • Asymmetric Synthesis and Catalysis
  • Radical Photochemical Reactions
  • Carbon dioxide utilization in catalysis
  • Catalytic Cross-Coupling Reactions
  • Oxidative Organic Chemistry Reactions
  • Fluorine in Organic Chemistry
  • Inorganic and Organometallic Chemistry
  • Various Chemistry Research Topics
  • Nanomaterials for catalytic reactions
  • Cyclopropane Reaction Mechanisms

Fudan University
2021-2023

Henan University
2017-2022

Kaifeng University
2019

Utah AIDS Foundation
1981

Abstract Reported herein is the first example of 2‐allylazaarenes in asymmetric catalysis. Highly γ‐selective allylation was demonstrated for activated ketones, including isatins and trifluoromethyl ketones. In presence either an amino‐acid‐based tertiary amine or quaternary ammonium salt catalyst, two series hydroxy‐containing moieties were installed at remote δ‐position azaarenes good chemical yields, excellent enantioselectivities, E / Z ratios. The success current reactions should...

10.1002/anie.201700190 article EN Angewandte Chemie International Edition 2017-02-27

An enantioconvergent substitution of 3-substituted 3-chlorooxindoles with N-aryl glycines under visible light irradiation is reported. A transition-metal-free cooperative catalysis platform a dicyanopyrazine-derived chromophore (DPZ) as photoredox catalyst and chiral Brønsted acid effective for these transformations, which involve single-electron transfer redox step an enantioselective radical coupling. variety valuable 3-aminomethylene-3-substituted oxindoles can be directly synthesized...

10.1039/c9cc05304b article EN Chemical Communications 2019-01-01

Phenols are pivotal precursors and core motifs for various fine chemicals, bioactive molecules, functional materials, among which the site-selective syntheses of ortho-substituted phenols very attractive challenging. Here, we present a palladium-catalyzed dehydrogenation–coupling–aromatization protocol to access from cyclohexanols with primary alcohols. Broad substrate scope was achieved in this modular water hydrogen gas as clean byproducts. The ortho-mono- ortho-disubstitutions were...

10.1021/acscatal.3c00826 article EN ACS Catalysis 2023-04-21

Abstract Reported herein is the first example of 2‐allylazaarenes in asymmetric catalysis. Highly γ‐selective allylation was demonstrated for activated ketones, including isatins and trifluoromethyl ketones. In presence either an amino‐acid‐based tertiary amine or quaternary ammonium salt catalyst, two series hydroxy‐containing moieties were installed at remote δ‐position azaarenes good chemical yields, excellent enantioselectivities, E / Z ratios. The success current reactions should...

10.1002/ange.201700190 article EN Angewandte Chemie 2017-02-27

Quaternary α-hydroxyl acids and their derivatives have attracted considerable attention because of unique broad functionalities. Herein, we successfully established a selective modular protocol to access quaternary acetates via dehydrogenative cross-coupling 1,2-diols primary alcohols by using tris-N-heterocyclic carbene iridium (tris-NHC-Ir, 0.05 mol %) complexes as catalysts Ba(OH)2 the base, along with generation byproducts water hydrogen gas. A plausible mechanism involving...

10.1021/acscatal.2c05820 article EN ACS Catalysis 2023-01-23
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