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PUBMED FOR HANDHELDS

Journal Abstract Search


220 related items for PubMed ID: 34958214

  • 21. Synthesis of Multisubstituted Allylic Alcohols via a Nickel-Catalyzed Cross-Electrophile Ring-Opening Reaction.
    Hu W, Lin Z, Wang C.
    Org Lett; 2022 Aug 12; 24(31):5751-5755. PubMed ID: 35901221
    [Abstract] [Full Text] [Related]

  • 22. Metallaphotoredox-Catalyzed Cross-Electrophile Csp3-Csp3 Coupling of Aliphatic Bromides.
    Smith RT, Zhang X, Rincón JA, Agejas J, Mateos C, Barberis M, García-Cerrada S, de Frutos O, MacMillan DWC.
    J Am Chem Soc; 2018 Dec 19; 140(50):17433-17438. PubMed ID: 30516995
    [Abstract] [Full Text] [Related]

  • 23. Nickel-catalyzed allylic substitution of simple alkenes.
    Matsubara R, Jamison TF.
    Chem Asian J; 2011 Jul 04; 6(7):1860-75. PubMed ID: 21387565
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  • 25. Ni-catalyzed migratory fluoro-alkenylation of unactivated alkyl bromides with gem-difluoroalkenes.
    Zhou L, Zhu C, Bi P, Feng C.
    Chem Sci; 2019 Jan 28; 10(4):1144-1149. PubMed ID: 30774912
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  • 27. Nickel-Catalyzed Directed Cross-Electrophile Coupling of Phenolic Esters with Alkyl Bromides.
    Yang F, Ding D, Wang C.
    Org Lett; 2020 Dec 04; 22(23):9203-9209. PubMed ID: 33210932
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  • 28. Nickel-catalyzed coupling of alkenes, aldehydes, and silyl triflates.
    Ng SS, Ho CY, Jamison TF.
    J Am Chem Soc; 2006 Sep 06; 128(35):11513-28. PubMed ID: 16939275
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  • 29. Synthesis of Tetrasubstituted Alkenes by Tandem Metallacycle Formation/Cross-Electrophile Coupling.
    Shimkin KW, Montgomery J.
    J Am Chem Soc; 2018 Jun 13; 140(23):7074-7078. PubMed ID: 29800523
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  • 31. Direct Synthesis of α-Aryl-α-Trifluoromethyl Alcohols via Nickel Catalyzed Cross-Electrophile Coupling.
    Lombardi L, Cerveri A, Giovanelli R, Castiñeira Reis M, Silva López C, Bertuzzi G, Bandini M.
    Angew Chem Int Ed Engl; 2022 Nov 21; 61(47):e202211732. PubMed ID: 36161744
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  • 33. Nickel-Catalyzed Alkyl-Alkyl Cross-Electrophile Coupling Reaction of 1,3-Dimesylates for the Synthesis of Alkylcyclopropanes.
    Sanford AB, Thane TA, McGinnis TM, Chen PP, Hong X, Jarvo ER.
    J Am Chem Soc; 2020 Mar 18; 142(11):5017-5023. PubMed ID: 32129601
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  • 35. Nickel-catalyzed stereoselective reductive cross-coupling of gem-difluoroalkenes with alkenyl electrophiles.
    Li X, Li Y, Shan W, Wang Z, Liu R, Zhang Z, Li X, Shi D.
    Chem Commun (Camb); 2023 Jun 01; 59(45):6893-6896. PubMed ID: 37199088
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  • 36. Defluorinative C(sp3 )-P Bond Construction for the Synthesis of Phosphorylation gem-Difluoroalkenes under Catalyst- and Oxidant-Free Conditions.
    Li C, Yuan JM, Chen W, He Y, Huang J, Huang Y, Xiao Q, Sheng J, Huang C.
    Chem Asian J; 2019 Aug 01; 14(15):2584-2587. PubMed ID: 31152631
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  • 37. Directed nickel-catalyzed negishi cross coupling of alkyl aziridines.
    Nielsen DK, Huang CY, Doyle AG.
    J Am Chem Soc; 2013 Sep 11; 135(36):13605-9. PubMed ID: 23961769
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  • 38. Nickel-Catalyzed Stereo- and Enantioselective Cross-Coupling of gem-Difluoroalkenes with Carbon Electrophiles by C-F Bond Activation.
    Zhu Z, Lin L, Xiao J, Shi Z.
    Angew Chem Int Ed Engl; 2022 Feb 01; 61(6):e202113209. PubMed ID: 34889493
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  • 40. Defluorinative alkylation of 1-trifluoromethyl alkenes with alkyl radicals derived from visible light-induced deoxygenation of xanthate salts: synthesis of gem-difluoroalkenes.
    Li X, Jiao Y, Han L, Sun J, Zhang X.
    Org Biomol Chem; 2023 Apr 26; 21(16):3330-3334. PubMed ID: 37013409
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