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Journal Abstract Search

134 related items for PubMed ID: 12616559

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  • 2. Chromium- and Metal-Reductant-Free Asymmetric Nozaki-Hiyama-Kishi (NHK) Reaction Enabled by Metallaphotoredox Catalysis.
    Gu P, Ding L, Fang X, Zhu J, Kang S, Wu B, Zhang J, Zhao Y, Shi Z.
    Angew Chem Int Ed Engl; 2024 Sep 09; 63(37):e202408195. PubMed ID: 38923245
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  • 4. Catalytic asymmetric Nozaki-Hiyama reactions with a tridentate bis(oxazolinyl)carbazole ligand.
    Inoue M, Suzuki T, Kinoshita A, Nakada M.
    Chem Rec; 2008 Sep 09; 8(3):169-81. PubMed ID: 18563811
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  • 5. Synthesis of the Core Framework of the Cornexistins by Intramolecular Nozaki-Hiyama-Kishi Coupling.
    Aimon A, Farrugia LJ, Clark JS.
    Molecules; 2019 Jul 22; 24(14):. PubMed ID: 31336669
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  • 8. A novel diastereoselective synthesis of (Z)-fluoroalkenes via a Nozaki-Hiyama-Kishi-type reaction.
    Dutheuil G, Lei X, Pannecoucke X, Quirion JC.
    J Org Chem; 2005 Mar 04; 70(5):1911-4. PubMed ID: 15730321
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  • 10. Cobalt-Catalyzed Asymmetric Migratory Nozaki-Hiyama-Kishi Coupling.
    Chen J, Wu L, Song Z, Wang Y, Li Z, Wang Y, Zhu S.
    J Am Chem Soc; 2024 Sep 25; 146(38):26223-26232. PubMed ID: 39284303
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  • 16. Electrocatalytic Asymmetric Nozaki-Hiyama-Kishi Decarboxylative Coupling: Scope, Applications, and Mechanism.
    Gao Y, Jiang B, Friede NC, Hunter AC, Boucher DG, Minteer SD, Sigman MS, Reisman SE, Baran PS.
    J Am Chem Soc; 2024 Feb 21; 146(7):4872-4882. PubMed ID: 38324710
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  • 17. The protecting-group directed diastereoselective Nozaki-Hiyama-Kishi (NHK) reaction: total synthesis and biological evaluation of zeaenol, 7-epi-zeaenol and its analogues.
    Mohapatra DK, Reddy DS, Mallampudi NA, Gaddam J, Polepalli S, Jain N, Yadav JS.
    Org Biomol Chem; 2014 Dec 21; 12(47):9683-95. PubMed ID: 25350150
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  • 18. Role of the Nozaki-Hiyama-Takai-Kishi Reaction in the Synthesis of Natural Products.
    Gil A, Albericio F, Álvarez M.
    Chem Rev; 2017 Jun 28; 117(12):8420-8446. PubMed ID: 28627170
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  • 20. Highly selective sulfoxidation of allylic and vinylic sulfides by hydrogen peroxide using a flavin as catalyst.
    Lindén AA, Krüger L, Bäckvall JE.
    J Org Chem; 2003 Jul 25; 68(15):5890-6. PubMed ID: 12868923
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