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Nathalie Hampel

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Chemistry (Weinheim an Der Bergstrasse, Germany)|November 20, 2020
Lewis Acidic Boranes, Lewis Bases, and Equilibrium Constants: A Reliable Scaffold for a Quantitative Lewis Acidity/Basicity ScaleRobert J Mayer, Nathalie Hampel, Armin R Ofial
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 29, 2003
Structure-nucleophilicity relationships for enaminesBernhard Kempf, Nathalie Hampel, Armin R Ofial, et al.
Organic Letters|September 16, 2015
Sequential Oxidative α-Cyanation/Anti-Markovnikov Hydroalkoxylation of AllylaminesAlexander Wagner, Nathalie Hampel, Hendrik Zipse, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 12, 2024
Defining the Synthetic Scope of ortho-Quinone Methides by Quantifying their ElectrophilicityChristoph Gross, Andreas Eitzinger, Nathalie Hampel, et al.
Acta Crystallographica. Section E, Structure Reports Online|May 18, 2011
4-[4-(Dimethyl-amino)benzyl-idene]-2,6-dimethyl-cyclo-hexa-2,5-dienoneNathalie Hampel, Dorothea Richter, Armin R Ofial, et al.
The Journal of Organic Chemistry|June 27, 2019
Ambident Reactivity of Phenolate Anions Revisited: A Quantitative Approach to Phenolate ReactivitiesRobert J Mayer, Martin Breugst, Nathalie Hampel, et al.
Organic Letters|March 3, 2020
Electrophilic Reactivities of Vinyl <i>p</i>-Quinone MethidesAndreas Eitzinger, Robert J Mayer, Nathalie Hampel, et al.
Chemical Science|June 24, 2021
Electrophilic reactivities of cyclic enones and α,β-unsaturated lactonesRobert J Mayer, Patrick W A Allihn, Nathalie Hampel, et al.
Chembiochem : a European Journal of Chemical Biology|May 21, 2025
Synthesis of Nucleoside Derivatives by Biomimetic Ester MigrationOliver Trapp, Nathalie J Kurrle, Christoph J B Seifert, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 20, 2020
Lewis Acidic Boranes, Lewis Bases, and Equilibrium Constants: A Reliable Scaffold for a Quantitative Lewis Acidity/Basicity ScaleRobert J Mayer, Nathalie Hampel, Armin R Ofial
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 29, 2003
Structure-nucleophilicity relationships for enaminesBernhard Kempf, Nathalie Hampel, Armin R Ofial, et al.
Organic Letters|September 16, 2015
Sequential Oxidative α-Cyanation/Anti-Markovnikov Hydroalkoxylation of AllylaminesAlexander Wagner, Nathalie Hampel, Hendrik Zipse, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 12, 2024
Defining the Synthetic Scope of ortho-Quinone Methides by Quantifying their ElectrophilicityChristoph Gross, Andreas Eitzinger, Nathalie Hampel, et al.
Acta Crystallographica. Section E, Structure Reports Online|May 18, 2011
4-[4-(Dimethyl-amino)benzyl-idene]-2,6-dimethyl-cyclo-hexa-2,5-dienoneNathalie Hampel, Dorothea Richter, Armin R Ofial, et al.
The Journal of Organic Chemistry|June 27, 2019
Ambident Reactivity of Phenolate Anions Revisited: A Quantitative Approach to Phenolate ReactivitiesRobert J Mayer, Martin Breugst, Nathalie Hampel, et al.
Organic Letters|March 3, 2020
Electrophilic Reactivities of Vinyl <i>p</i>-Quinone MethidesAndreas Eitzinger, Robert J Mayer, Nathalie Hampel, et al.
Chemical Science|June 24, 2021
Electrophilic reactivities of cyclic enones and α,β-unsaturated lactonesRobert J Mayer, Patrick W A Allihn, Nathalie Hampel, et al.
Chembiochem : a European Journal of Chemical Biology|May 21, 2025
Synthesis of Nucleoside Derivatives by Biomimetic Ester MigrationOliver Trapp, Nathalie J Kurrle, Christoph J B Seifert, et al.
Pageof 1