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Structural, Kinetic, and Computational Characterization of the Elusive Arylpalladium(II)boronate Complexes in the Suzuki–Miyaura Reaction

from the Scott E. Denmark group

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  • A.A. Thomas, H. Wang, A.F. Zahrt, and S.E. Denmark, "Structural, Kinetic, and Computational Characterization of the Elusive Arylpalladium(II)boronate Complexes in the Suzuki–Miyaura Reaction", Journal of the American Chemical Society, vol. 139, pp. 3805-3821, 2017. http://dx.doi.org/10.1021/jacs.6b13384
  • A Method for Identifying and Developing Functional Group Tolerant Catalytic Reactions: Application to the Buchwald–Hartwig Amination

    [Lilly]

    [1]
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  • J. Richardson, J.C. Ruble, E.A. Love, and S. Berritt, "A Method for Identifying and Developing Functional Group Tolerant Catalytic Reactions: Application to the Buchwald–Hartwig Amination", The Journal of Organic Chemistry, vol. 82, pp. 3741-3750, 2017. http://dx.doi.org/10.1021/acs.joc.7b00201
  • Development and Demonstration of a Safer Protocol for the Synthesis of 5-Aryltetrazoles from Aryl Nitriles

    [tetrazoles, Bristol-Myers Squibb]

    [1]

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  • D.S. Treitler, S. Leung, and M. Lindrud, "Development and Demonstration of a Safer Protocol for the Synthesis of 5-Aryltetrazoles from Aryl Nitriles", Organic Process Research & Development, vol. 21, pp. 460-467, 2017. http://dx.doi.org/10.1021/acs.oprd.7b00016
  • C(sp3)-C(sp2) cross-coupling of alkylsilicates with borylated aryl bromides – an iterative platform to alkylated aryl- and heteroaryl boronates


    [1]

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  • B.A. Vara, M. Jouffroy, and G.A. Molander, "C(sp3)–C(sp2) cross-coupling of alkylsilicates with borylated aryl bromides – an iterative platform to alkylated aryl- and heteroaryl boronates", Chemical Science, vol. 8, pp. 530-535, 2017. http://dx.doi.org/10.1039/C6SC03236B