Yuchen Zhou

ORCID: 0009-0007-6216-9708
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About
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Research Areas
  • Synthesis and Catalytic Reactions
  • Catalytic C–H Functionalization Methods
  • Radical Photochemical Reactions
  • Cyclopropane Reaction Mechanisms
  • Organic Chemistry Cycloaddition Reactions
  • Catalytic Cross-Coupling Reactions
  • Carbon dioxide utilization in catalysis
  • N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
  • Analytical Chemistry and Chromatography
  • Computational Drug Discovery Methods
  • Synthesis and Biological Evaluation
  • Oxidative Organic Chemistry Reactions
  • Asymmetric Hydrogenation and Catalysis
  • Toxin Mechanisms and Immunotoxins
  • Insect and Pesticide Research
  • Molecular spectroscopy and chirality
  • Botanical Research and Chemistry

The University of Queensland
2024

Nanjing Tech University
2023

Wuhan University
2017

A method for electrooxidative C(sp3)–H amination via intermolecular oxidative C(sp3)–H/N–H cross-coupling has been developed under metal- and oxidant-free conditions. The bonds adjacent to oxygen, nitrogen, sulfur atoms could all react smoothly with various amines give the corresponding products moderate good yields (30–93%). In addition, of benzylic allylic are also tolerated in this reaction. preliminary mechanistic study indicates that C–H cleavage tetrahydrofuran is probably not involved...

10.1021/acscatal.7b03551 article EN ACS Catalysis 2017-10-26

A photoredox-catalyzed 1,2-amidoheteroarylation of unactivated alkenes with O-acyl hydroxylamine derivatives and heterocycles is presented. range heterocycles, including quinoxaline-2(1H)-ones, azauracils, chromones, quinolones, are capable for this process, allowing the direct synthesis valuable heteroarylethylamine derivatives. Structurally diverse reaction substrates, drug-based scaffolds, were successfully applied, demonstrating practicality method.

10.1021/acs.orglett.3c01376 article EN Organic Letters 2023-05-30

A novel method of palladium-catalyzed oxidative carbonylation ketones, amines, and carbon monoxide for the synthesis 4-quinolones has been developed. This protocol provides a straightforward route to construct useful 4-quinolone derivatives from inexpensive chemicals.

10.1021/acs.orglett.7b03337 article EN Organic Letters 2017-11-16

Pimelea poisoning of Australian cattle is attributed to the natural toxin simplexin binding bovine PKC. Molecular dynamics simulations reveal simplexin's high affinity for PKC, and identify SAR future molecular interventions against poisoning.

10.1039/d4ob00065j article EN Organic & Biomolecular Chemistry 2024-01-01

Unexpectedly facile dearomative intramolecular (4+3) cycloadditions of thiophenes with epoxy enolsilanes, providing sulfur-bridged cycloadducts, are reported. A total fifteen thiophene substrates have been found to undergo cycloaddition smoothly produce endo and exo adducts in yields up 83 % moderate good diastereoselectivity. Complete conservation enantiomeric purity was observed when the optically enriched epoxide used. The desulfurizing transformations skeleton cycloadducts provide...

10.1002/anie.202407059 article EN Angewandte Chemie International Edition 2024-05-17

Abstract Unexpectedly facile dearomative intramolecular (4+3) cycloadditions of thiophenes with epoxy enolsilanes, providing sulfur‐bridged cycloadducts, are reported. A total fifteen thiophene substrates have been found to undergo cycloaddition smoothly produce endo and exo adducts in yields up 83 % moderate good diastereoselectivity. Complete conservation enantiomeric purity was observed when the optically enriched epoxide used. The desulfurizing transformations skeleton cycloadducts...

10.1002/ange.202407059 article EN Angewandte Chemie 2024-05-17
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