Financial supports were obtained from the National Natural Science Foundation of China(NSFC,grant nos.22025103,22331006,92256301,22371112,and 22101122);the National Key R&D Program of China(grant nos.2021YFF0701604 and 2021YFF0701704);Guangdong Major Project of Basic and Applied Basic Research,China(grant no.2023B0303000020);Guangdong Basic and Applied Basic Research Foundation,China(grant no.2023A1515140088);Shenzhen Science and Technology Program,China(grant nos.JCYJ20220818100600001,JCYJ202205300115409020,and 20220814231741002);the Shenzhen Key Laboratory of Cross-Coupling Reactions,China(grant no.ZDSYS20220328104200001);Dongguan Key Laboratory of Interdisciplinary Science for Advanced Materials and Large-Scale Scientific Facilities,China(grant no.2023KSYS014);Also,the New Cornerstone Science Foundation through the XPLORER PRIZE is gratefully acknowledged.
The asymmetric radical carboamination of 1,1-disubstituted alkenes from readily available alkyl halides and arylamines provides expedient access to valueadded chiralα-tertiary N-arylamines but has been less recognize...
Supporting information for this article is available on the WWW under http://dx.doi.org/10.1002/cjoc,201700280 or from the author.Acknowledgement The work was partially supported by the National Natural Science Foundation of China (No. 21172001, 21372008), the Natural Science Foundation of Education Administration of Anhui Province (KJ2016A267), the Special and Excellent Research Fund of Anhui Normal University and the Doctoral Scientific Research Foundation of Anhui Normal University (No. 2016XJJ110).
A green and highly efficient synthetic method for the synthesis of quinazoline-2,4-diones with hydrogen peroxide as the terminal oxidant has been developed, The reaction features the mild reaction conditions, broad su...
With the support by the National Natural Science Foundation of China,the research team led by Prof.Chang Mingxin(常明欣)at the Department of Chemistry and Chemical Engineering,Northwest A&F University,has developed a ...
supported by the Opening Project of Key Laboratory at Universities of Education Department of Xinjiang Uygur Autonomous Region (No. 2014YSHXZD01)
A simple and metal-free method has been developed for the construction of quinoline-2,4-carboxylates under mild conditions via a molecular iodine-catalyzed three-component tandem reaction of arylamines, ethyl glyoxyla...
supported by the National Natural Science Foundation of China (No. 31170539)
Two dehydroabietic acid-based arylamines have been synthesized and characterized by FTIR, 1H NMR, 13C NMR, MS spectra and elemental analysis. Their spatial structures were determined by X-ray diffraction analysis. UV-...
Under the catalysis of Lewis acid Co(CIO4)2 the reaction of the sterically hindered 1,1,2,3-tetrasubstituted cyclopropanes with arylamines in refluxing THF gave the functionalized 2-aminopyrroles with sequential rin...
A simple and efficient methodology for the synthesis of triphenylamines has been demonstrated using copper catalyst with a ligand and tripotassium phosphate as the base. The effect of parameters such as catalyst precu...
support from National Basic Research Program of China(973 Program, No2012CB214900);the National Natural Science Foundation of China(No21176246);the Fundamental Research Funds for the Central Universities
Thiazoles including five 2-arylbenzothiazoles and two 2-arylnaphthothiazoles were synthesized using a simple synthetic strategy in this work.2-Arylbenzothiazoles and 2-arylnaphthothiazoles can be prepared by the react...
Supported by the National Natural Science Foundation of China(No.20572058)
CuCl-catalyzed oxidative N-demethylation of arylamines proceeded in the presence of tert-butyl hydroperoxide. The one-electron transfer route of oxidative N-demethylation competed favorably with the H-atom abstraction...
Project supported by the National Natural Science Foundation of China(No.20172016);Shanghai Science&Technology Council(04JC14032).
Suzuki cross-coupling reaction of phenylboronic acid with aryl halides catalyzed by cyclopalladated complexes of tertiary arylamines immobilized in ionic liquid [Bmim]^+BF4^- was reported. The catalytic system proved...