Wang Lab@SIOC
@pengwanglab
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Synthetic organic chemistry lab @ SIOC, metal catalysis, main group chemistry, asymmetric catalysis.
Shanghai
Joined March 2014
Photoredox/Ni-Catalytic Synthesis of cis-Vinyl Iodides from Acetylene | Journal of the American Chemical Society
pubs.acs.org
The stereoselective synthesis of cis-vinyl iodides represents a long-standing challenge in organic synthesis, with Stork–Zhao olefination remaining the benchmark methodology since its inception in...
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“My parents could barely read or write. It’s been quite a journey, science allows you to do it.” New laureate Omar Yaghi was in the middle of changing flights when we reached him, just after he heard that he had been awarded the 2025 #NobelPrize in Chemistry. In this interview
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Three scientists win Nobel Prize in chemistry for the development of metal-organic frameworks
phys.org
Three scientists won the Nobel Prize in chemistry Wednesday for their development of new molecular structures that can trap vast quantities of gas inside, laying the groundwork to potentially suck...
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Just out @ChemicalScience One more example of Migratory 1,n-Cycloannulation Reaction (MCAR) of alkenes for modular and diverse synthesis of oxaheterocycles. Check out: https://t.co/CN0rGRcg8n
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We have realized the modular and diverse synthesis of oxaheterocycles via Pd-catalyzed migratory 1,n-cycloannulation of alkenes. Check out our recent preprint @ChemRxiv
https://t.co/lw6iKLe3v7
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Prof. Jin-Quan Yu (@YulabJin) will receive the 5th Akira Suzuki Award for his research on C–H bond activation, which makes it easier to build complex molecules. His work accelerates advances in pharmaceuticals, molecular tools and materials science. More:
magazine.scripps.edu
Jin-Quan Yu, the Bristol Myers Squibb Endowed Chair in Chemistry and the Frank and Bertha Hupp Professor in Chemistry at Scripps Research, has been selected as the recipient of the 5th Akira Suzuki...
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This work was previously deposited @ChemRxiv on October 4, 2024. Available at:
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Finally out @ChemicalScience We have realized a Rh-Catalyzed Enantioselective Hydrosilylation of Unactivated Alkenes. Congrats to Yichen, Hao-Yang and Heng. Check out here: https://t.co/48p7dRkBpY
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Cu-Catalyzed Enantioselective Carbene Insertion into Ge–H and Si–H Bonds Enabled by SPSiBox with a Tunable Chiral Pocket | Journal of the American Chemical Society
pubs.acs.org
Here, we report the Cu-catalyzed asymmetric carbene insertion into both Ge–H and Si–H bonds with α-trifluoromethyl diazo compounds, enabled by a class of newly developed C2-symmetrical bisoxazoline...
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Congratulations to Alex! He has prepared a nice review on the catalytic atroposelective construction of diaryl ethers and diaryl amines. Just out @ACSCatalysis | https://t.co/AtD0SlDllE
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Finally out in JACS. Congrats to Shi-Hao and Sheng-Ye. We have developed an SPSiOL-based bisoxazoline ligand (SPSiBox), featuring a tunable chiral pocket. Plz check out here: https://t.co/WmDoKD4MhR
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Check out our recent publication @EurJOC We have realized the direct coupling of polyfluoroarenes with acylsilanes using t-AmylONa as a catalytic base. See: https://t.co/4u5JPzXoIC
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Direct Coupling of Polyfluoroarenes with Acylsilanes: Introduction of polyfluoro(hetero)aryl groups under metal-free conditions https://t.co/C33V9lQmZN
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Atroposelective Diverse Remote meta-C–H Functionalization via Kinetic Resolution | Journal of the American Chemical Society @TotalSyntheses @scrippsresearch
@YulabJin
pubs.acs.org
A diverse range of Pd(II)-catalyzed enantioselective C–H activation reactions have been developed to construct point, axial, and planar chirality. Despite the importance of chiral biaryl scaffolds in...
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EnantioCH by our MPAA ligand fills a gap in chiral technology; creating new chemical space for both drug discovery and chiral ligands: https://t.co/i2vTTsP4uZ
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With a bulky acac-type ligand (Amacac), Ni(II)-catalyzed dicarbofunctionalization of alkenyl alcohols has been realized using alcohol as the native DG. The final version of this manuscript out in @ChemCatalysis Congrats to Li-Qin. Check out: https://t.co/5ukcN58ZdB
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Facile Access to Quaternary Carbon Centers via Ni-Catalyzed Arylation of Alkenes with Organoborons | Journal of the American Chemical Society @TotalSyntheses
pubs.acs.org
Quaternary carbon centers are widespread structural motifs, thus representing extensive interest in organic synthesis. We describe here an efficient nickel-catalyzed intermolecular, Markovnikov-sel...
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Another nice example of Ni-catalyzed hydroarylation of alkenes with arylborons for accessing quaternary carbon centers. Check out this one @J_A_C_S collaborated with Prof. Shi-Liang Shi. https://t.co/cNISsTgaL6
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We are excited to announce our “Best Cover” contest, celebrating the most outstanding covers published in Organic Chemistry Frontiers. You are welcome to take part in this voting task: 🔗 https://t.co/a6vMC5oByJ
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Pd-Catalyzed Migratory 1,1-Cycloannulation Reaction of Alkenes | Journal of the American Chemical Society @TotalSyntheses #Pd #Catalysis #Cycloannulation #Alkenes
pubs.acs.org
Here, we report a novel strategy for the preparation of diverse heterocycles via a Pd-catalyzed migratory 1,1-cycloannulation reaction (MCAR) of alkenes. Starting from readily available alkenyl...
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