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Dong D, Tian B, Yang H, Wei Z, Yang S, Zhou M, Ding C, Wang Y, Gao J, Wang S, Yang W, Liu B, Wang Z. Visible light induced palladium-catalyzed reactions involving halogenated hydrocarbon (RX). Molecular Catalysis 2023;541:113073. [DOI: 10.1016/j.mcat.2023.113073] [Reference Citation Analysis]
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Xian N, Yin J, Ji X, Deng GJ, Huang H. Visible-Light-Mediated Photoredox Carbon Radical Formation from Aqueous Sulfoxonium Ylides. Org Lett 2023;25:1161-5. [PMID: 36757126 DOI: 10.1021/acs.orglett.3c00143] [Reference Citation Analysis]
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Liu D, Zhao Y, Patureau FW. NaI/PPh(3)-catalyzed visible-light-mediated decarboxylative radical cascade cyclization of N-arylacrylamides for the efficient synthesis of quaternary oxindoles. Beilstein J Org Chem 2023;19:57-65. [PMID: 36741816 DOI: 10.3762/bjoc.19.5] [Reference Citation Analysis]
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Zhang L, He J, Shen J, Xu H, Zhu D, Shen C. Highly efficient synthesis of C3-heteroaryl 3-fluorooxindoles via a one-pot stepwise Ce(iii)/photoassisted cross-dehydrogenative coupling/fluorooxidation process. Org Chem Front 2023. [DOI: 10.1039/d2qo01599d] [Reference Citation Analysis]
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Chen L, Jiang K, Zeng G, Yin B. Photoinduced Pd-Catalyzed Csp2–H/Csp3–H Dehydrocoupling Reaction Employing Polyhaloaromatics as the Dehydrogenating Agent. Org Lett 2022. [DOI: 10.1021/acs.orglett.2c03708] [Reference Citation Analysis]
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Fan X, Liu H, Ma S, Wang F, Yang J, Li D. Visible light-induced PPh2Cy/CsI-promoted cascade radical decarboxylative/cyclization of redox-active esters with acrylamides. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132849] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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Chen S, Van Meervelt L, Van der Eycken EV, Sharma UK. Visible-Light-Driven Palladium-Catalyzed Radical Tandem Dearomatization of Indoles with Unactivated Alkenes. Org Lett 2022. [PMID: 35107015 DOI: 10.1021/acs.orglett.1c04390] [Reference Citation Analysis]
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Wu X, Zhao F, Ji X, Huang H. Visible Light-Assisted Photocatalyst-Free Tandem Sulfonylation/ Cyclization for the Synthesis of Oxindoles. Chinese Journal of Organic Chemistry 2022;42:4323. [DOI: 10.6023/cjoc202208036] [Reference Citation Analysis]
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Sun Z, Huang H, Wang Q, Huang C, Mao G, Deng G. Visible light-mediated radical-cascade addition/cyclization of arylacrylamides with aldehydes to form quaternary oxindoles at room temperature. Org Chem Front 2022;9:3506-14. [DOI: 10.1039/d2qo00319h] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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Zhang MZ, Li WT, Li YY, Wang Q, Li C, Liu YH, Yin JX, Yang X, Huang H, Chen T. Discovery of an Oxidative System for Radical Generation from Csp3-H Bonds: A Synthesis of Functionalized Oxindoles. J Org Chem 2021;86:15544-57. [PMID: 34570502 DOI: 10.1021/acs.joc.1c02032] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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Muralirajan K, Kancherla R, Gimnkhan A, Rueping M. Unactivated Alkyl Chloride Reactivity in Excited-State Palladium Catalysis. Org Lett 2021;23:6905-10. [PMID: 34432470 DOI: 10.1021/acs.orglett.1c02467] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 3.5] [Reference Citation Analysis]
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