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Articles by Congyang Wang
A high-energy hydrogen radical initiates efficient electrosynthesis of urea from CO 2 and N 2
Abstract The electrochemical co-reduction of CO2 and N2 to urea presents a sustainable alternative to conventional synthesis but faces substantial challenges. Here we design a catalyst by anchoring the ionic liquid (IL) 1-ethyl-2,3-dimethylimidazolium bromide onto a CuBi surface. The IL@CuBi catalyst delivers an exceptional Faradaic efficiency toward urea (FEurea) of 73.0% and a current density of 27.4 mA cm−2 in an H-type cell, with a production rate of 124.7 μmol cm−2 h−1.
Proton-Regulated C–N Coupling for Efficient Amino Acid Electrosynthesis
Cite Jump to ExpandCollapse ArticleDecember 10, 2025 Proton-Regulated C–N Coupling for Efficient Amino Acid Electrosynthesis Click to copy article linkArticle link copied! Yong Wang Yong Wang Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Centre for Excellence in Molecular Sciences, Centre for Carbon Neutral Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China Xiang-Da...
Proton-Regulated C–N Coupling for Efficient Amino Acid Electrosynthesis
Journal of the American Chemical Society Cite this: J. Am. Chem. Soc. 2025, XXXX, XXX Click to copy citationCitation copied! Learn about these metrics Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days. Citations are the number of other articles citing this article, calculated by Crossref and updated daily.
Umpolung Coupling of Pyridine-2-carboxaldehydes and Propargylic Carbonates via N-Heterocyclic Carbene/Palladium Synergetic Catalysis
Umpolung Coupling of Pyridine-2-carboxaldehydes and Propargylic Carbonates via N-Heterocyclic Carbene/Palladium Synergetic Catalysis The umpolung cross-coupling reaction of pyridine-2-carboxaldehydes and propargylic carbonates has been developed for the first time through N-heterocyclic carbene/palladium cooperative catalysis with the judicious selections of the palladium catalyst, ligand and N-heterocyclic carbene, giving the propargylic ketones regioselectively.
Manganese‐Catalyzed Hydroarylation of Unactivated Alkenes
Communication Congyang Wang Corresponding Author E-mail address: wangcy@iccas.ac.cn Institute of Chemistry, Chinese Academy of Sciences, CAS Key Laboratory of Molecular Recognition and Function, Zhongguancun North First Street 2, 100190 Beijing, CHINA Search for more papers by this author Abstract Transition‐metal‐catalyzed hydroarylation of unactivated alkenes with strategic use of remote coordinating functional groups has received significant attentions recently in order to address the...
Manganese‐Catalyzed Redox‐Neutral C−H Olefination of Ketones with Unactivated Alkenes
As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re‐organized for online delivery, but are not copy‐edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors.
Manganese‐Catalyzed Redox‐Neutral C‐H Olefination of Ketones with Unactivated Alkenes
As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re‐organized for online delivery, but are not copy‐edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors.
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