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Synthesis of (+)-Vitepyrroloid A and (+)-Vitepyrroloid B by Late-Stage Ni-Catalyzed C(sp2)–C(sp3) Cross-Electrophile Coupling


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  • M. Menger, D. Lentz, and M. Christmann, "Synthesis of (+)-Vitepyrroloid A and (+)-Vitepyrroloid B by Late-Stage Ni-Catalyzed C(sp2)–C(sp3) Cross-Electrophile Coupling", The Journal of Organic Chemistry, vol. 83, pp. 6793-6797, 2018. http://dx.doi.org/10.1021/acs.joc.8b00882
  • Nickel-Catalyzed Reductive Cross-Coupling of Aryl Halides with Monofluoroalkyl Halides for Late-Stage Monofluoroalkylation



    [1]

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  • J. Sheng, H. Ni, H. Zhang, K. Zhang, Y. Wang, and X. Wang, "Nickel-Catalyzed Reductive Cross-Coupling of Aryl Halides with Monofluoroalkyl Halides for Late-Stage Monofluoroalkylation", Angewandte Chemie International Edition, vol. 57, pp. 7634-7639, 2018. http://dx.doi.org/10.1002/anie.201803228
  • Elucidating the Role of the Boronic Esters in the Suzuki–Miyaura Reaction: Structural, Kinetic, and Computational Investigations

    from the Scott E. Denmark group

    [1]

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  • A.A. Thomas, A.F. Zahrt, C.P. Delaney, and S.E. Denmark, "Elucidating the Role of the Boronic Esters in the Suzuki–Miyaura Reaction: Structural, Kinetic, and Computational Investigations", Journal of the American Chemical Society, vol. 140, pp. 4401-4416, 2018. http://dx.doi.org/10.1021/jacs.8b00400
  • A platform for automated nanomole-scale reaction screening and micromole-scale synthesis in flow

    [Pfizer]

    [1]

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  • D. Perera, J.W. Tucker, S. Brahmbhatt, C.J. Helal, A. Chong, W. Farrell, P. Richardson, and N.W. Sach, "A platform for automated nanomole-scale reaction screening and micromole-scale synthesis in flow", Science, vol. 359, pp. 429-434, 2018. http://dx.doi.org/10.1126/science.aap9112
  • Esterification of Carboxylic Acids with Difluoromethyl Diazomethane and Interrupted Esterification with Trifluoromethyl Diazomethane: A Fluorine Effect


    [1]

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  • S. Peng, X. Zhang, L. Zhang, and X. Hu, "Esterification of Carboxylic Acids with Difluoromethyl Diazomethane and Interrupted Esterification with Trifluoromethyl Diazomethane: A Fluorine Effect", Organic Letters, vol. 19, pp. 5689-5692, 2017. http://dx.doi.org/10.1021/acs.orglett.7b02866
  • Exploiting a “Beast” in Carbenoid Chemistry: Development of a Straightforward Direct Nucleophilic Fluoromethylation Strategy


    [1]

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  • G. Parisi, M. Colella, S. Monticelli, G. Romanazzi, W. Holzer, T. Langer, L. Degennaro, V. Pace, and R. Luisi, "Exploiting a “Beast” in Carbenoid Chemistry: Development of a Straightforward Direct Nucleophilic Fluoromethylation Strategy", Journal of the American Chemical Society, vol. 139, pp. 13648-13651, 2017. http://dx.doi.org/10.1021/jacs.7b07891
  • The Direct C–H Difluoromethylation of Heteroarenes Based on the Photolysis of Hypervalent Iodine(III) Reagents That Contain Difluoroacetoxy Ligands


    [1]

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  • R. Sakamoto, H. Kashiwagi, and K. Maruoka, "The Direct C–H Difluoromethylation of Heteroarenes Based on the Photolysis of Hypervalent Iodine(III) Reagents That Contain Difluoroacetoxy Ligands", Organic Letters, vol. 19, pp. 5126-5129, 2017. http://dx.doi.org/10.1021/acs.orglett.7b02416