the National Key R&D Program of China(No.2021YFF1200203 to G.W.and 2018YFA0903500 to F.Z.);Hubei Provincial Key R&D program(2021BAA168 to Y.W.);Shen-Zhen Science and Technology Program(JCYJ20220530160805011 to F.Z.);the interdisciplinary research program of Huazhong University of Science and Technology(HUST)(2023JCYJ001 to F.Z.);the China Postdoctoral Science Foundation(2023M741259 to X.Y.)for financial supports.
Comprehensive Summary The implementation of divergent protein engineering on the natural transaminase Vf-ω-TA led to the development of two effective mutants(M2 and M8),enabling the enzymatic synthesis of chiral amin...
the financial support from the National Natural Science Foundation of China(21801129,22078153 and 22378201);National Key Research and Development Program of China(2022YFB3805603);Natural Science Research Projects in Jiangsu Higher Education Institutions(18KJB150018);Nanjing Tech University(Start-up Grant Nos.39837137,39837101 and 3827401739)for financial support.
A visible-light-induced photoredox-catalyzed regioselective and stereoselective C(sp')-H amination of enamides with bench-stable and A visible-light-induced photoredox-catalyzed regioselective and stereoselective C(sp...
support from the National Key R&D Program of China (2022YFA1503703,2021YFF0701604);the National Natural Science Foundation of China (21825105,22231004,22271135);Guangdong Innovative Program (2019BT02Y335);Shenzhen Science and Technology Program (KQTD20210811090112004,JCYJ20210324120205016,JCYJ20210324105005015).
Indole-based atropisomers are a very important class of axially chiral compounds.However,the atroposelective synthesis of axially chiral 2-arylindole remains largely unexplored.In this study,we report the successful s...
National Key Research and Development Program of China(2022YFA1503200,2021YFC2101901);the National Natural Science Foundation of China(22122103,22101130,22001117,21971108,22271144);Fundamental Research Funds for the Central Universities(020514380304,020514380252,020514380272)for financial support.
In this paper,we have developed a decarboxylative amination of carboxylic acids with nitroarenes for the synthesis of secondary amines.The protocol is performed at mild conditions without the use of noble metals as ca...
the National Natural Science Foundation of China(22201048);the Natural Science Foundation of Guangxi Province(2022GXNSFBA035480);the Specific Research Project of Guangxi for Research Bases and Talents(2022AC21099);the Start-up Fund of Guangxi University(A3040051013)for financial support.
A one-pot synthesis of vicinal diamines using indoles,azoles and phenothiazines in a tandem multi-component reaction is developed.The utilization of a copper-iodine co-catalytic system enables the generation of a dive...
The structure of Montelukast-derivatives(12)in Table 2 and the structure of its product 25 in page s24 are wrong,and they should be Montelukast-derivatives(12)methyl(R,E)-2-(1-(1-(3-(2-(7-chloroquinolin-2-yl)vinyl)phe...
the European Research Council(ERC)under the European Union's Horizon 2020 research and innovation programme(grant agreement No.883212).
Comprehensive Summary Enantioselective or enantioconvergent iron-catalyzed ring-closing C(sp^(3))-H aminations of N-aroyloxyurea through intermediate iron nitrene species provide chiral 2-imidazolidinones in up to 99%...
the National Natural Science Foundation of China(21925108,21901203,21901204)for financial support.
Comprehensive Summary A general and efficient strategy for the synthesis ofγ-lactams has been reported.The hydroxylamines form Lossen rearrangement products of electron-deficient group migration with base and then un...
financial support from the National Natural Science Foundation of China(Grant Nos.21901216 and 82074003,82174083);the Funds of Sichuan Science and Technology Program(23NSFSC0862,2021YFSY0041,2021YFH0064 and 2021ZHFP0032);the Opening subject under KF-202204 in the State Key Laboratory of Pharmaceutical Biotechnology,Nanjing University,China,the Fund of Science and Technology Agency of Chengdu(2019-YF09-00049-SN);the research project of the Administration of Traditional Chinese Medicine of Sichuan(2021MS110);the Open Project Program of Irradiation Preservation Technology Key Laboratory of Sichuan Province,Sichuan Institute of Atomic Energy(No.FZBC2020002);the Fundamental Research Funds for the Central Universities(2682020ZT85).
The visible light-driven C2 or C3 amination of indoles without any additives was initiated via electron donor-acceptor (EDA) complex formed by indole and N-aminopyridinium salt.This method was compatible with a wide r...
NSFC(Grant No.22171186) and ShanghaiTech University start-up funding for financial support;the support from Analytical Instrumentation Center(contract no.SPST-AIC10112914),SPST。
An efficient kinetic resolution(KR)protocol for 1,2-diamines has been developed through asymmetric electrophilic aminations of anilines enabled by chiral phosphoric acid catalysis.A wide array of substituted 1,2-diami...