financially supported by Shandong Provincial Natural Science Foundation(No.ZR2022MB120&ZR2020MB048);the University Feature Laboratory for Energy Conversion and Nanocatalysis of Shandong Province;Hundred Outstanding Talent Program of Jining University(No.2020ZYRC05).
We present a facile synthetic strategy to create mesoporous Cu_(2)O nanocrystals with tunable pore structures and surface functional groups of amine derivatives for efficient and preferable electrochemical conversion ...
We thank the support from National Key R&D Program of China(2022YFA1504302,2021YFF0701603);National Natural Science Foundation of China(U22A20388,92256302,21925109 for B.-F.S.,22271250 for T.Z.);Fundamental Research Funds for the Central Universities(226-2023-00115,226-2022-00224,226-2022-00175);Zhejiang Provincial NSFC(LD22B030003)。
Axially chiral N-arylindoles bearing a stereogenic C—N axis are unique important scaffolds in natural products,advance materials,pharmaceuticals and privileged chiral ligands or catalysts.Herein,we report the direct ...
We are grateful for the financial support from the NSFC(21931006 and 21961132004);the Fundamental Research Funds for the Central Universities,and China Postdoctoral Science Foundation(2019M663488);Postdoctoral Foundation of Sichuan University(2020SCU12019).
Asymmetric aminocatalysis has become one of the most powerful strategies for the transformations of carbonyl substances over the past two decades.Here,we describe the research from our laboratory that significantly ex...
What is the most favorite and original chemistry developed in your research group? Developing PIP amine for regio-and enantioselective methylene C-H activation. How do you get into this specific field? Could you pleas...
grants from the National Key Technology R&D Program(No.2016YFD0400801);the National Natural Science Foundation of China(No.21871019).
An efficient electrochemical access to the non-symmetric biphenols using tri(p-bromophenyl)amine(TBPA)as a redox mediator has been developed.The electrochemical protocol features highly selective cross-coupling produc...
the National Natural Science Foundation of China (Nos.91534114,21622308);the Key Program Supported by the Natural Science Foundation of Zhejiang Province, China (No.LZ18B060002];the Fundamental Research Funds for the Central Universities (No.2017XZZXO02-16).
The National Key R&D Program of China (Nos.2015CB856600, 2016YFA0202900);the National Natural Science Foundation of China (Nos.21422209,21432011,21421091,21572255);Chinese Academy of Sciences (No.XDB20000000).
This research was supported by the National Natural Science Foundation of China (Nos. 21672199 and 21790333) and CAS Interdisciplinary Innovation Team.
A new palladium-catalyzed selective aminomethylation of conjugated 1,3-dienes with aminais via double C-N bond activation is described. This simple method provides an effective and rapid approach for the synthesis of ...
Nucleophilic addition of primary aromatic amines to carbodiimides in the presence of catalytic amount of the mono-indenyl-ligated rare earth metal bis(silylamide) complexes (C9H6CMe2CHzCsH4N-a)Ln[N(SiHMe2)2]2 at...
A novel PdC12/bis(2-pyridylmethyl)amine-based ligand (1) catalytic system, which is water-soluble and air-stable, has been successfully synthesized and applied for Suzuki-Miyaura cross-coupling reaction. In the pr...