Herbert Mayr, Ph.D.

Affiliations: 
1984 University of Munich, München, Bayern, Germany 
Website:
http://www.cup.uni-muenchen.de/oc/mayr/CDmayrcv.html
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Jangra H, Chen Q, Fuks E, et al. (2018) Nucleophilicity and Electrophilicity Parameters for Predicting Absolute Rate Constants of Highly Asynchronous 1,3-Dipolar Cycloadditions of Aryldiazomethanes. Journal of the American Chemical Society
Timofeeva DS, Ofial AR, Mayr H. (2018) Kinetics of Electrophilic Fluorinations of Enamines and Carbanions: Comparison of the Fluorinating Power of N-F Reagents. Journal of the American Chemical Society
Li Z, Jangra H, Chen Q, et al. (2018) Kinetics and Mechanism of Oxirane Formation by Darzens Condensation of Ketones: Quantification of the Electrophilicities of Ketones. Journal of the American Chemical Society
Timofeeva DS, Mayer R, Mayer P, et al. (2018) Which Factors Control the Nucleophilic Reactivities of Enamines? Chemistry (Weinheim An Der Bergstrasse, Germany)
Allgäuer DS, Jangra H, Asahara H, et al. (2017) Quantification and Theoretical Analysis of the Electrophilicities of Michael Acceptors. Journal of the American Chemical Society
Mayer R, Tokuyasu T, Mayer P, et al. (2017) Solvation Accounts for the Counter-Intuitive Nucleophilicity Ordering of Peroxide Anions. Angewandte Chemie (International Ed. in English)
Li Z, Chen Q, Mayer P, et al. (2017) Nucleophilicity parameters of arylsulfonyl substituted halomethyl anions. The Journal of Organic Chemistry
Byrne PA, Kobayashi S, Würthwein EU, et al. (2017) Why are Vinyl Cations Sluggish Electrophiles? Journal of the American Chemical Society
Levens A, An F, Breugst M, et al. (2016) Influence of the N-Substituents on the Nucleophilicity and Lewis Basicity of N-Heterocyclic Carbenes. Organic Letters
Chelli S, Troshin K, Mayer P, et al. (2016) Nucleophilicity Parameters of Stabilized Iodonium Ylides for Characterizing their Synthetic Potential. Journal of the American Chemical Society
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