the financial support from the National Natural Science Foundation of China(22001121);Nanjing Tech University。
A catalyst-free and additive-free ring-opening reaction of polyfluoroalkyl peroxides,triethylenediamine(DABCO),and 1,2-dichloroethane(DCE)has been developed for the defluorinative synthesis of structurally diverse pip...
financial support from National Natural Science Foundation of China(Nos.21801129,22078153 and22378201);National Key Research and Development Program of China(No.2022YFB3805603);Natural science research projects in Jiangsu Higher Education Institutions(No.18KJB150018);Open Research Fund of School of Chemistry and Chemical Engineering;Henan Normal University(No.2024Y16);Nanjing Tech University(Start-up Grant Nos.39837137,39837101 and 3827401739)for financial support。
Pyridyl-based ketones and 1,6-diketones are both attractive and invaluable scaffolds which play pivotal roles in the construction and structural modification of a plethora of synthetically paramount natural products,p...
supported by the National Natural Science Foundation of China(22271127,22071084);the Fundamental Research Funds for the Central Universities(lzujbky-2022-ey01)。
Reactions involving alkenyl acetates offer cost-effective and environmentally friendly routes for alkene synthesis,yet their asymmetric variant remains elusive.Concurrently,asymmetric conjugate alkenylation predominan...
supported by the National Natural Science Foundation of China(22002067,22202228);the Fund Program for the Scientific Activities of Selected Returned Overseas Professionals in Shanxi Province(20220052);the Science and Technology Project of Shanxi Province(202103021223457,202303021221256);Research Project Supported by Shanxi Scholarship Council of China.
Catalytic dehydrogenation,with its exceptional atom economy and chemoselectivity,offers a highly desirable yet challenging approach for converting multiple environmentally friendly alcohols into crucial molecules.Furt...
funding supports from the National Natural Science Foundation of China(Nos.21732002,22061007,22071036,and 22207022);Frontiers Science Center for Asymmetric Synthesis and Medicinal Molecules,National Natural Science Fund for Excellent Young Scientists Fund Program(Overseas),the starting grant of Guizhou University[No.(2022)47)];Department of Education,Guizhou Province[Qianjiaohe KY No.(2020)004];The 10 Talent Plan(Shicengci)of Guizhou Province(No.[2016]5649);Science and Technology Department of Guizhou Province(Nos.[Qiankehe-jichu-ZK[2022]zhongdian024],[2018]2802,[2019]1020,QKHJC-ZK[2022]-455);Department of Education of Guizhou Province(No.QJJ(2022)205);Program of Introducing Talents of Discipline to Universities of China(111 Program,No.D20023)at Guizhou University;Singapore National Research Foundation under its NRF Investigatorship(No.NRF-NRFI2016–06);Competitive Research Program(No.NRF-CRP22–2019–0002);Ministry of Education,Singapore,under its MOE Ac RF Tier 1 Award(Nos.RG7/20,RG70/21);MOE AcRF Tier 2(No.MOE2019-T2–2–117);MOE AcRF Tier 3 Award(No.MOE2018-T3–1–003);a Chair Professorship Grant,and Nanyang Technological University。
Enones are widely explored in synthetic chemistry as fundamental building blocks for a wide range of reactions and exhibit intriguing biological activities that are pivotal for drug discovery.The development of synthe...
supported by the National Natural Science Foundation of China(22171072,21925103,22301061);Henan Normal University。
Direct enantioselective reduction of the C=C bond ofβ-polyfluoro-alkylated enones is an important but long-pending subject in asymmetric catalysis.Here,we report on the viability of visible light-driven cooperative p...
the financial support for this investigation from the National Natural Science Foundation of China(No.22072111;the Fundamental Research Funds for the Central Universities(No.2023IVA055).
Nucleophilic phosphine and amine catalyst-switched chemodivergent[4+1]and[3+3]annulations of allenyl imides andβ,γ-enones have been developed,furnishing highly substituted 2-cyclopentenone and 2-pyranone derivatives...
supported by the National Natural Science Foundation of China (Nos. 21801067, U1804283, 21801066);the Central Plains Scholars and Scientists Studio Fund (No. 2018002);the Project funded by the Natural Science Foundation of Henan (Nos. 202300410225, 212300410181, 222102310562 and 201901023);China Postdoctoral Science Foundation (Nos. 2020T130176 and 2020M682306);financial support from Henan Key Laboratory of Organic Functional Molecules and Drug Innovation
Ni(0)-catalyzed regio-and diastereodivergent[4+2]annulation of biphenylenes withα,βunsaturated ketones is described.This solvent-controlled diastereodivergent reaction integrates C-C bond cleavage of biphenylene and...
supported by the National Natural Science Foundation of China(Nos.22073066,21503143 and 21975179);the Natural Science Foundation of Tianjin(No.16JCQNJC05600)。
Density functional theory calculations have been performed to investigate the dipeptide phosphinecatalyzed hydroamination of enones with pyridazinones.The computations reveal that a number of the N-H...O hydrogen-bond...
the financial support from the National Natural Science Foundation of China(No.21921002);the NationalScience and Technology Major Project of the Ministry of Science and Technology of the People’s Republic of China(No.2018ZX09711001-005-004);the Fundamental Research Funds for the Central Universities(No.2012017yjsy210)。
A convergent approach to 1,5-hydroxy ketones,the general precursors for constructing the C ring of bryostatins,has been developed via a Zn/Cu-promoted conjugate addition of a-hydroxy iodides with enones.The reaction l...