Yu Han

ORCID: 0000-0003-0502-6245
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About
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Research Areas
  • Catalytic C–H Functionalization Methods
  • Radical Photochemical Reactions
  • Oxidative Organic Chemistry Reactions
  • Asymmetric Synthesis and Catalysis
  • Sulfur-Based Synthesis Techniques
  • Optical measurement and interference techniques
  • Advanced Fiber Laser Technologies
  • Cyclopropane Reaction Mechanisms
  • Synthesis and Catalytic Reactions
  • Photonic Crystal and Fiber Optics
  • Chemical Synthesis and Analysis
  • Gas Sensing Nanomaterials and Sensors
  • Transition Metal Oxide Nanomaterials
  • Laser-Matter Interactions and Applications
  • Synthesis of heterocyclic compounds
  • Advanced Chemical Sensor Technologies
  • Structural Health Monitoring Techniques
  • Catalytic Alkyne Reactions
  • Image Processing Techniques and Applications
  • Natural product bioactivities and synthesis
  • Fluorine in Organic Chemistry
  • Chemical Synthesis and Reactions
  • Synthesis and Reactivity of Heterocycles
  • Metalloenzymes and iron-sulfur proteins
  • Bioactive Compounds and Antitumor Agents

Linyi University
2019-2025

Sichuan University
2017-2025

Shandong University of Technology
2024-2025

Jiangxi Normal University
2023-2025

Anyang Normal University
2025

Chinese Academy of Medical Sciences & Peking Union Medical College
2024

Tianjin University
2023

Chengdu University
2017-2021

Hefei National Center for Physical Sciences at Nanoscale
2018

University of Science and Technology of China
2018

Photocatalysis opens up a new window for carbonyl chemistry. Despite multitude of photochemical reactions compounds, visible light-induced catalytic asymmetric transformations remain elusive and pose formidable challenge. Accordingly, the development simple, efficient, economic systems is ideal pursuit chemists. Herein, we report an enantioselective radical photoaddition to ketones through Lewis acid-enabled photoredox catalysis wherein in situ formed chiral N,N'-dioxide/Sc(III)-ketone...

10.1021/jacs.2c09691 article EN Journal of the American Chemical Society 2022-11-22

Enantioselective photoreduction of ketones with hydrocarbons is promising for the straightforward construction chiral tertiary alcohols. But it generally promoted by ultraviolet light via ketyl radical–alkyl radical coupling, which suffers from a competitive charge-transfer process and self/cross coupling reactions. An appropriate selection catalyst that can alter reaction pathway deliver spatial required. Accordingly, we disclosed combined system involving Er(III)-based Lewis acid...

10.1021/acscatal.2c00789 article EN ACS Catalysis 2022-04-15

Visible light‐mediated enantioselective alkylation of carbonyls with hydrocarbons provides a beneficial access to the synthesis chiral alcohols in terms atom economy. Herein, we disclosed direct asymmetric a‐keto pyrazoleamides as C(sp3)–H donors for preparation tertiary a‐hydroxy amides. Our method operates by synergistic catalysis involving Ir‐based photoredox catalyst and N,N′‐dioxide‐NiBr2 complex enabled addition reaction good excellent yield enantioselectivity (up 87% 97% ee),...

10.1002/cctc.202402112 article EN ChemCatChem 2025-02-14

A 2-alkenoylpyridine-bound N,N'-dioxide-TbIII complex has been found to absorb visible light reach the excited state, leading direct visible-light-excited catalytic enantioselective [2+2] cycloaddition of 2-alkenoylpyridines various alkenes in absence an additional photosensitizer. Diverse enantioenriched cyclobutanes were successfully obtained (yields up 70 %, >19:1 d.r., 92 % ee). The new chiral terbium(III) features a bathochromic shift, lower excitation energy, and facile intersystem...

10.1002/chem.201804600 article EN Chemistry - A European Journal 2018-10-20

The direct α-alkylation of acyclic carbonyls with nonactivated hydrocarbons through C(sp3 )-H functionalization is both extremely promising and notably challenging, especially when attempting to achieve enantioselectivity using iron-based catalysts. We have identified a robust chiral iron complex for the oxidative cross-coupling 2-acylimidazoles benzylic allylic hydrocarbons, as well alkanes. readily available tunable N,N'-dioxide catalysts in connection oxidants exhibit precise asymmetric...

10.1002/anie.202314256 article EN Angewandte Chemie International Edition 2023-11-21

A chiral <italic>N</italic>,<italic>N</italic>′-dioxide/Tb(OTf)<sub>3</sub> complex catalyzed diastereo- and enantioselective [4+3] cycloaddition of <italic>ortho</italic>-quinone methides with oxiranes has been described in this study.

10.1039/d1cc00262g article EN Chemical Communications 2021-01-01

In this paper, we report the use of CoTe2 nanosheet polyvinyl alcohol composites as saturable absorbers for pulse generation in erbium-doped fiber lasers. The absorption characteristics nanosheets have been investigated, and their modulation depth saturation intensity are 3.64% 1.25 MW/cm2, respectively. By controlling pump power polarization controller, conversion from dark–bright–dark pulses to h-shaped rains can be achieved laser. This mode-locked state transition occurs because nonlinear...

10.1021/acsanm.4c00178 article EN ACS Applied Nano Materials 2024-03-12

The complex alignment of 2-lane roads results in a higher risk traffic crashes. This study aims to identify key factors influencing vehicle driving states on curves. Five curve radii were selected create simulated scenarios. Vehicle operation data collected from 36 drivers using simulator. speed and lateral lane position chosen as indicators states. A 3-factor analysis variance (ANOVA) was conducted assess the effects radius, direction, position. Polynomial fitting models also developed...

10.1080/15389588.2024.2447088 article EN Traffic Injury Prevention 2025-02-21

A practical and effective copper-catalyzed dehydrogenative Diels–Alder reaction of gem-diesters ketone with dienes has been established. The active dienophiles were generated in situ via a radical-based dehydrogenation process, which reacted wide variety to afford various polysubstituted cyclohexene derivatives good excellent yields.

10.1021/acs.orglett.8b01067 article EN Organic Letters 2018-05-23

An unexpected homologation/dyotropic rearrangement/interconversion/[3+2] cycloaddition cascade reaction of α-diazoester-terminated N-propyl-substituted isatin derivatives was achieved in the presence a chiral N,N'-dioxide/ScIII catalyst. This catalytic manifold allows rapid construction several classes dimeric polycyclic compounds with good yields and high levels diastereo- enantioselectivity (up to 99 % ee). Furthermore, macrocyclic dimers can be obtained by an intermolecular homologation process.

10.1002/anie.201810030 article EN Angewandte Chemie International Edition 2018-10-23

Here we report an efficient asymmetric [4+2] cycloaddition of β,γ-unsaturated α-ketoesters with cyclobutenones. The corresponding products were obtained in good yields (up to 92%) excellent enantioselectivities 98% ee) and diastereoselectivities >19/1 dr). Moreover, based on the control experiments previous reports, a possible catalytic cycle was proposed.

10.1039/c8cc01040d article EN Chemical Communications 2018-01-01

Highly efficient asymmetric intermolecular radical-polar crossover reactions were realized by combining a chiral N,N'-dioxide/NiII complex catalyst with Ag2 O under mild reaction conditions. Various terminal alkenes and indanonecarboxamides/esters underwent radical addition/cyclization to afford spiro-iminolactones spirolactones good excellent yields (up 99 %) enantioselectivities 97 % ee). Furthermore, range of different radical-mediated oxidation/elimination or epoxide ring-opening...

10.1002/anie.201914151 article EN Angewandte Chemie International Edition 2020-01-13

The in-plane orientations of Si/SiC heterojunctions on 6H-SiC(0001) were investigated by high-resolution X-ray diffraction. An Si(111)/SiC(0001) heterostructure with an orientation Si[01−1]//SiC[110] is achieved at 900 °C, the Si/6H-SiC interface has a 4 : 5 Si-to-SiC matching mode residual lattice mismatch 0.26%, and edge dislocation density calculated to be 4.87 × 1013 cm−2. As growth temperature increased 1050 [110] preferential Si[−110]//SiC[0−10] observed, along Si[001]SiC[210]...

10.1039/c6ce00137h article EN CrystEngComm 2016-01-01
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