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26Juil 2017

Forging Quaternary Fluorine Stereocenters by a Light-driven Organocatalytic Aldol Desymmetrization Process

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[1]

  • S. Cuadros, L. Dell'Amico, and P. Melchiorre, "Forging Fluorine-Containing Quaternary Stereocenters by a Light-Driven Organocatalytic Aldol Desymmetrization Process", Angewandte Chemie International Edition, vol. 56, pp. 11875-11879, 2017. http://dx.doi.org/10.1002/anie.201706763
    • 24Juil 2017

    Silicon-Based Reagents for Difluoromethylation and Difluoromethylenation Reactions

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    [1]

  • S. Krishnamoorthy, and G. Prakash, "Silicon-Based Reagents for Difluoromethylation and Difluoromethylenation Reactions", Synthesis, vol. 49, pp. 3394-3406, 2017. http://dx.doi.org/10.1055/s-0036-1588489
    • 20Juil 2017

    Introduction of Trifluoroethylamine as Amide Isostere by C–H Functionalization of Heteroarenes

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    [with Genetech]

    [1]

  • M. Braun, G. Castanedo, L. Qin, P. Salvo, and S.Z. Zard, "Introduction of Trifluoroethylamine as Amide Isostere by C–H Functionalization of Heteroarenes", Organic Letters, vol. 19, pp. 4090-4093, 2017. http://dx.doi.org/10.1021/acs.orglett.7b01880
    • 20Juil 2017

    Radical Difluoromethylation of Thiols with (Difluoromethyl)triphenylphosphonium Bromide

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    [1]

  • N.B. Heine, and A. Studer, "Radical Difluoromethylation of Thiols with (Difluoromethyl)triphenylphosphonium Bromide", Organic Letters, vol. 19, pp. 4150-4153, 2017. http://dx.doi.org/10.1021/acs.orglett.7b02109
    • 19Juil 2017

    Pd-Catalyzed Decarbonylative Cross-Couplings of Aroyl Chlorides

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    [1]

  • C.A. Malapit, N. Ichiishi, and M.S. Sanford, "Pd-Catalyzed Decarbonylative Cross-Couplings of Aroyl Chlorides", Organic Letters, vol. 19, pp. 4142-4145, 2017. http://dx.doi.org/10.1021/acs.orglett.7b02024
    • 18Juil 2017

    A Two-Step, One-Pot, and Multigram-Scale Synthesis of N-Difluoromethylthiophthalimide

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    [1]

  • D. Zhu, X. Hong, D. Li, L. Lu, and Q. Shen, "A Two-Step, One-Pot, and Multigram-Scale Synthesis of N-Difluoromethylthiophthalimide", Organic Process Research & Development, vol. 21, pp. 1383-1387, 2017. http://dx.doi.org/10.1021/acs.oprd.7b00203
    • 13Juil 2017

    Electrochemical Nickel Catalysis for Sp2-Sp3 Cross-Electrophile Coupling Reactions of Unactivated Alkyl Halides

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    [1]

  • R.J. Perkins, D.J. Pedro, and E.C. Hansen, "Electrochemical Nickel Catalysis for Sp2-Sp3 Cross-Electrophile Coupling Reactions of Unactivated Alkyl Halides", Organic Letters, vol. 19, pp. 3755-3758, 2017. http://dx.doi.org/10.1021/acs.orglett.7b01598
    • 13Juil 2017

    Recyclable Trifluoromethylation Reagents from Fluoroform

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    [1]

  • J.B. Geri, and N.K. Szymczak, "Recyclable Trifluoromethylation Reagents from Fluoroform", Journal of the American Chemical Society, vol. 139, pp. 9811-9814, 2017. http://dx.doi.org/10.1021/jacs.7b05408
    • 12Juil 2017

    Trifluoromethylation of Alkyl Radicals in Aqueous Solution

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    [1]

  • H. Shen, Z. Liu, P. Zhang, X. Tan, Z. Zhang, and C. Li, "Trifluoromethylation of Alkyl Radicals in Aqueous Solution", Journal of the American Chemical Society, vol. 139, pp. 9843-9846, 2017. http://dx.doi.org/10.1021/jacs.7b06044
    • 06Juil 2017

    Coupling of Challenging Heteroaryl Halides with Alkyl Halides via Nickel-Catalyzed Cross-Electrophile Coupling

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    Pfizer, Asymchem & Weix

    [1]

  • E.C. Hansen, C. Li, S. Yang, D. Pedro, and D.J. Weix, "Coupling of Challenging Heteroaryl Halides with Alkyl Halides via Nickel-Catalyzed Cross-Electrophile Coupling", The Journal of Organic Chemistry, vol. 82, pp. 7085-7092, 2017. http://dx.doi.org/10.1021/acs.joc.7b01334
    • 06Juil 2017

    Radical Difluororomethylation of Thiols with Difluoromethylphosphonium Triflate under Photoredox Catalysis

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    [1]

  • Y. Ran, Q. Lin, X. Xu, and F. Qing, "Radical Difluororomethylation of Thiols with Difluoromethylphosphonium Triflate under Photoredox Catalysis", The Journal of Organic Chemistry, vol. 82, pp. 7373-7378, 2017. http://dx.doi.org/10.1021/acs.joc.7b01041
    • 04Juil 2017

    SuFEx-Based Polysulfonate Formation from Ethenesulfonyl Fluoride-Amine Adducts

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    [1]

  • H. Wang, F. Zhou, G. Ren, Q. Zheng, H. Chen, B. Gao, L. Klivansky, Y. Liu, B. Wu, Q. Xu, J. Lu, K.B. Sharpless, and P. Wu, "SuFEx-Based Polysulfonate Formation from Ethenesulfonyl Fluoride-Amine Adducts", Angewandte Chemie International Edition, vol. 56, pp. 11203-11208, 2017. http://dx.doi.org/10.1002/anie.201701160

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