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Armin R Ofial

Showing results (31-40 of 70) with videos related to

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European Journal of Organic Chemistry|July 7, 2020
CF<sub>3</sub>-Containing <i>para</i>-Quinone Methides for Organic SynthesisMichael Winter, Roman Schütz, Andreas Eitzinger, et al.
Journal of the American Chemical Society|January 9, 2020
Basicities and Nucleophilicities of Pyrrolidines and Imidazolidinones Used as OrganocatalystsFeng An, Biplab Maji, Elizabeth Min, 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.
Chemical Communications (Cambridge, England)|June 9, 2023
The effect of Magenta J Hensinger, Anna C Closs, Oliver Trapp, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 4, 2017
Reactivity-Tuning in Frustrated Lewis Pairs: Nucleophilicity and Lewis Basicity of Sterically Hindered PhosphinesElsa Follet, Peter Mayer, David S Stephenson, et al.
Journal of the American Chemical Society|January 24, 2025
Highly Nucleophilic Pyridinamide Anions in Apolar Organic Solvents due to Asymmetric Ion Pair AssociationVeronika Burger, Maximilian Franta, 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.
Journal of the American Chemical Society|July 29, 2009
Can one predict changes from S(N)1 to S(N)2 mechanisms?Thanh Binh Phan, Christoph Nolte, Shinjiro Kobayashi, et al.
Angewandte Chemie (International Ed. in English)|January 22, 2015
Fine-tuning the nucleophilic reactivities of boron ate complexes derived from aryl and heteroaryl boronic estersGuillaume Berionni, Artem I Leonov, Peter Mayer, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|December 7, 2005
How fast do R-X bonds ionize? A semiquantitative approachBernard Denegri, Armin R Ofial, Sandra Jurić, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
European Journal of Organic Chemistry|July 7, 2020
CF<sub>3</sub>-Containing <i>para</i>-Quinone Methides for Organic SynthesisMichael Winter, Roman Schütz, Andreas Eitzinger, et al.
Journal of the American Chemical Society|January 9, 2020
Basicities and Nucleophilicities of Pyrrolidines and Imidazolidinones Used as OrganocatalystsFeng An, Biplab Maji, Elizabeth Min, 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.
Chemical Communications (Cambridge, England)|June 9, 2023
The effect of Magenta J Hensinger, Anna C Closs, Oliver Trapp, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 4, 2017
Reactivity-Tuning in Frustrated Lewis Pairs: Nucleophilicity and Lewis Basicity of Sterically Hindered PhosphinesElsa Follet, Peter Mayer, David S Stephenson, et al.
Journal of the American Chemical Society|January 24, 2025
Highly Nucleophilic Pyridinamide Anions in Apolar Organic Solvents due to Asymmetric Ion Pair AssociationVeronika Burger, Maximilian Franta, 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.
Journal of the American Chemical Society|July 29, 2009
Can one predict changes from S(N)1 to S(N)2 mechanisms?Thanh Binh Phan, Christoph Nolte, Shinjiro Kobayashi, et al.
Angewandte Chemie (International Ed. in English)|January 22, 2015
Fine-tuning the nucleophilic reactivities of boron ate complexes derived from aryl and heteroaryl boronic estersGuillaume Berionni, Artem I Leonov, Peter Mayer, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|December 7, 2005
How fast do R-X bonds ionize? A semiquantitative approachBernard Denegri, Armin R Ofial, Sandra Jurić, et al.
Pageof 7