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  • 52. Chapter 7. Markovnikov Functionalization by Hydrogen Atom Transfer

    52. Chapter 7. Markovnikov Functionalization by Hydrogen Atom Transfer

    52. Matos, J. L. M.; Green, S. A.; Shenvi, R. A. Chapter 7. Markovnikov Functionalization by Hydrogen Atom Transfer, Organic Reactions, 2019, 100, 383–470.

  • 50. Hydroalkylation of Olefins to form Quaternary Carbons

    50. Hydroalkylation of Olefins to form Quaternary Carbons

    50. Green, S. A.; Huffman, T. R.; McCourt, R. O.; van der Puyl, V.; Shenvi, R. A. Hydroalkylation of Olefins to form Quaternary Carbons J. Am. Chem. Soc. 2019, 141, 7709-7714.

  • 46. Branch-Selective Addition of Unactivated Olefins into Imines and Aldehydes

    46. Branch-Selective Addition of Unactivated Olefins into Imines and Aldehydes

    46. Matos, J.L.M.; Vásquez-Céspedes, S.; Gu, J.; Oguma, T.; Shenvi, R.A. Branch-Selective Addition of Unactivated Olefins into Imines and Aldehydes J. Am. Chem. Soc. 2018, 140, 16976–16981.

  • 45. The High Chemofidelity of Metal-Catalyzed Hydrogen Atom Transfer 

    45. The High Chemofidelity of Metal-Catalyzed Hydrogen Atom Transfer 

    45. Green, S.A.; Crossley, S.W.M.; Matos, J.L.M.; Vásquez-Céspedes, S.; Shevick, S. L.; Shenvi, R. A. The High Chemofidelity of Metal-Catalyzed Hydrogen Atom Transfer Acc. Chem. Res., 2018, 51, 2628–2640.

  • 44. Mechanistic Interrogation of Co/Ni-Dual Catalyzed Hydroarylation

    44. Mechanistic Interrogation of Co/Ni-Dual Catalyzed Hydroarylation

    44. Shevick, S. L.; Obradors, C.; Shenvi, R. A. Mechanistic Interrogation of Co/Ni-Dual Catalyzed Hydroarylation J. Am. Chem. Soc. 2018,140, 12056–12068.

  • 43. Iron-Nickel Dual-Catalysis: A New Engine for Olefin Functionalization

    43. Iron-Nickel Dual-Catalysis: A New Engine for Olefin Functionalization

    43. Green, S. A.; Vásquez-Céspedes, S.; Shenvi, R. A. Iron-Nickel Dual-Catalysis: A New Engine for Olefin Functionalization. J. Am. Chem. Soc. 2018, 140, 11317–11324

  • 35. Branch-Selective Hydroarylation: Iodoarene-Olefin Cross Coupling

    35. Branch-Selective Hydroarylation: Iodoarene-Olefin Cross Coupling

    35. Green, S. A.; Matos, J. L. M.; Yagi, A.; Shenvi, R. A. Branch-Selective Hydroarylation: Iodoarene-Olefin Cross Coupling. J. Am. Chem. Soc. 2016, 138, 12779-12782.

  • 33. Mn, Fe, and Co-Catalyzed Radical Hydrofunctionalizations of Olefins

    33. Mn, Fe, and Co-Catalyzed Radical Hydrofunctionalizations of Olefins

    33. Crossley, S. W. M.; Martinez, R. M.; Obradors, C.; Shenvi, R. A. Mn, Fe, and Co-Catalyzed Radical Hydrofunctionalizations of Olefins. Chem. Rev. 2016, 116, 8912-9000.

  • 30. Synthesis of the Privileged 8-Arylmenthol Class by Radical Arylation of Isopulegol

    30. Synthesis of the Privileged 8-Arylmenthol Class by Radical Arylation of Isopulegol

    30. Crossley, S. W. M.; Martinez, R. M.; Zuluaga, S. G.; Shenvi R. A. Synthesis of the Privileged 8-Arylmenthol Class by Radical Arylation of Isopulegol. Org. Lett. 2016, 18, 2620-2623.

  • 29. An Exceptional Reductant for Metal-Catalyzed Hydrogen Atom Transfers

    29. An Exceptional Reductant for Metal-Catalyzed Hydrogen Atom Transfers

    29. Obradors, C. L.; Martinez, R.; Shenvi, R. A. Ph(i-PrO)SiH2: An Exceptional Reductant for Metal-Catalyzed Hydrogen Atom Transfers. J. Am. Chem. Soc. 2016, 138, 4962-4971.

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