Roland Appel |
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Dissertation | Phosphorus Ylides, Sulfur Ylides, and Related Carbanions as Reference Nucleophiles for the Quantification of the Electrophilic Reactivities of Aldehydes, Imines, and Enones (04/2011) [pdf] |
Awards | |
Award of the Dr. Klaus Römer-Stiftung for PhD students (2011). | |
Publications | |
Quantification of Ion-Pairing Effects on the Nucleophilic Reactivities of Benzoyl- and Phenyl-Substituted Carbanions in Dimethylsulfoxide
F. Corral Bautista, R. Appel, J. S. Frickel, H. Mayr, Chem. Eur. J. 2015, 21, 875-884. [download] |
Electrophilicities of Benzaldehyde-Derived Iminium Ions: Quantification of the Electrophilic Activation of Aldehydes by Iminium Formation R. Appel, S. Chelli, T. Tokuyasu, K. Troshin, H. Mayr, J. Am. Chem. Soc. 2013, 135, 6579-6587. [download] |
Quantification of the Electrophilic Reactivities of Aldehydes, Imines, and Enones
R. Appel, H. Mayr, J. Am. Chem. Soc. 2011,133, 8240-8251. [download] |
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Scope and Limitations of Cyclopropanations with Sulfur Ylides
R. Appel, N. Hartmann, H. Mayr, J. Am. Chem. Soc. 2010, 132, 17894-17900. [download] |
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Nucleophilic Reactivities of Sulfur Ylides and Related Carbanions: Comparison with Structurally Related Organophosphorus Compounds
R. Appel, H. Mayr, Chem. Eur. J. 2010, 16, 8610-8614. [download] |
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Wie werden Iminium-katalysierte
Cyclopropanierungen durch elektrostatische Aktivierung gesteuert?
How Does Electrostatic Activation Control Iminium Catalyzed Cyclopropanations? S. Lakhdar, R. Appel, H. Mayr, Angew. Chem. 2009, 121, 5134-5137; Angew. Chem. Int. Ed. 2009, 48, 5034-5037. [deutsch-download][english-download] |
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Nucleophilicity Parameters
for Phosphoryl-Stabilized Carbanions and Phosphorus Ylides: Implications
for Wittig and Related Olefination Reactions
R. Appel, R. Loos, H. Mayr, J. Am. Chem. Soc. 2009, 131, 704-714. [download] |
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Nucleophilicities of
the Anions of Arylacetonitriles and Arylpropionitriles in Dimethyl Sulfoxide
O. Kaumanns, R. Appel, T. Lemek, F. Seeliger, H. Mayr, J. Org. Chem. 2009, 74, 75-81. [download] |