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Journal Abstract Search

159 related items for PubMed ID: 27723164

  • 1. Structures, Lewis Acidities, Electrophilicities, and Protecting Group Abilities of Phenylfluorenylium and Tritylium Ions.
    Follet E, Mayer P, Berionni G.
    Chemistry; 2017 Jan 12; 23(3):623-630. PubMed ID: 27723164
    [Abstract] [Full Text] [Related]

  • 2. Reactivity-Tuning in Frustrated Lewis Pairs: Nucleophilicity and Lewis Basicity of Sterically Hindered Phosphines.
    Follet E, Mayer P, Stephenson DS, Ofial AR, Berionni G.
    Chemistry; 2017 Jun 01; 23(31):7422-7427. PubMed ID: 28370848
    [Abstract] [Full Text] [Related]

  • 3. Philicities, Fugalities, and Equilibrium Constants.
    Mayr H, Ofial AR.
    Acc Chem Res; 2016 May 17; 49(5):952-65. PubMed ID: 27108991
    [Abstract] [Full Text] [Related]

  • 4. Scales of Lewis basicities toward C-centered Lewis acids (carbocations).
    Mayr H, Ammer J, Baidya M, Maji B, Nigst TA, Ofial AR, Singer T.
    J Am Chem Soc; 2015 Feb 25; 137(7):2580-99. PubMed ID: 25555037
    [Abstract] [Full Text] [Related]

  • 5. Nucleophilicity of Alkyl Zirconocene and Titanocene Precatalysts, and Kinetics of Activation by Carbenium Ions and by B(C6 F5 )3.
    Berionni G, Kurouchi H, Eisenburger L, Mayr H.
    Chemistry; 2016 Aug 01; 22(32):11196-200. PubMed ID: 27245119
    [Abstract] [Full Text] [Related]

  • 6. How constant are Ritchie's "constant selectivity relationships"? A general reactivity scale for n-, pi-, and sigma-nucleophiles.
    Minegishi S, Mayr H.
    J Am Chem Soc; 2003 Jan 08; 125(1):286-95. PubMed ID: 12515531
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  • 8. Lewis Acidity Scale of Diaryliodonium Ions toward Oxygen, Nitrogen, and Halogen Lewis Bases.
    Mayer RJ, Ofial AR, Mayr H, Legault CY.
    J Am Chem Soc; 2020 Mar 18; 142(11):5221-5233. PubMed ID: 32125154
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  • 10. Which Factors Control the Nucleophilic Reactivities of Enamines?
    Timofeeva DS, Mayer RJ, Mayer P, Ofial AR, Mayr H.
    Chemistry; 2018 Apr 17; 24(22):5901-5910. PubMed ID: 29388720
    [Abstract] [Full Text] [Related]

  • 11. Nucleophilicity and nucleofugality of phenylsulfinate (PhSO(2)(-)): a key to understanding its ambident reactivity.
    Baidya M, Kobayashi S, Mayr H.
    J Am Chem Soc; 2010 Apr 07; 132(13):4796-805. PubMed ID: 20225879
    [Abstract] [Full Text] [Related]

  • 12. A practical guide for estimating rates of heterolysis reactions.
    Streidl N, Denegri B, Kronja O, Mayr H.
    Acc Chem Res; 2010 Dec 21; 43(12):1537-49. PubMed ID: 21082867
    [Abstract] [Full Text] [Related]

  • 13. Reference scales for the characterization of cationic electrophiles and neutral nucleophiles.
    Mayr H, Bug T, Gotta MF, Hering N, Irrgang B, Janker B, Kempf B, Loos R, Ofial AR, Remennikov G, Schimmel H.
    J Am Chem Soc; 2001 Oct 03; 123(39):9500-12. PubMed ID: 11572670
    [Abstract] [Full Text] [Related]

  • 14. Nucleophilicities and carbon basicities of pyridines.
    Brotzel F, Kempf B, Singer T, Zipse H, Mayr H.
    Chemistry; 2007 Oct 03; 13(1):336-45. PubMed ID: 17009366
    [Abstract] [Full Text] [Related]

  • 15. Carbanion reactivity, kinetic and equilibrium studies of sigma-adduct formation and elimination in the reactions of 4-nitrobenzofurazan derivatives with nitroalkane anions.
    Asghar BH, Crampton MR.
    Org Biomol Chem; 2007 May 21; 5(10):1646-54. PubMed ID: 17571196
    [Abstract] [Full Text] [Related]

  • 16. A quantitative approach to nucleophilic organocatalysis.
    Mayr H, Lakhdar S, Maji B, Ofial AR.
    Beilstein J Org Chem; 2012 May 21; 8():1458-78. PubMed ID: 23019481
    [Abstract] [Full Text] [Related]

  • 17. Basicities and Nucleophilicities of Pyrrolidines and Imidazolidinones Used as Organocatalysts.
    An F, Maji B, Min E, Ofial AR, Mayr H.
    J Am Chem Soc; 2020 Jan 22; 142(3):1526-1547. PubMed ID: 31913030
    [Abstract] [Full Text] [Related]

  • 18. Highly efficient Lewis acid catalytic activity of the tritylium ion at the node of a tensile organic framework.
    Zhao S, Zhang J, Zhai Y, Zou X, Wang S, Bian Z, Cui F, Zhu G.
    Chem Sci; 2021 Jul 21; 12(28):9786-9793. PubMed ID: 34349952
    [Abstract] [Full Text] [Related]

  • 19. Evidence that protons can be the active catalysts in Lewis acid mediated hetero-Michael addition reactions.
    Wabnitz TC, Yu JQ, Spencer JB.
    Chemistry; 2004 Jan 23; 10(2):484-93. PubMed ID: 14735517
    [Abstract] [Full Text] [Related]

  • 20. Methylene Bridging Effect on the Structures, Lewis Acidities and Optical Properties of Semi-planar Triarylboranes.
    Doan TH, Chardon A, Osi A, Mahaut D, Tumanov N, Wouters J, Champagne B, Berionni G.
    Chemistry; 2021 Jan 21; 27(5):1736-1743. PubMed ID: 32852852
    [Abstract] [Full Text] [Related]

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