Author

Marco Pappini

Institution: University of Milan

Observed institution: University of Milan

OpenAlex ID: A5090769738

Inherently Chiral Macrocyclic Oligothiophenes: Easily Accessible Electrosensitive Cavities with Outstanding Enantioselection Performances

2014 · Francesco Sannicolò, Patrizia R. Mussini, et al. · Chemistry - A European Journal · 68

Thiol‐disulfide redox equilibria of glutathione metaboloma compounds investigated by tandem mass spectrometry

2008 · Federico M. Rubino, Marco Pitton, et al. · Rapid Communications in Mass Spectrometry · 13

Measurement of S‐methylcysteine and S‐methyl‐mercapturic acid in human urine by alkyl‐chloroformate extractive derivatization and isotope‐dilution gas chromatography–mass spectrometry

2010 · Federico M Rubino, Marco Pitton, et al. · Biomedical Chromatography · 11

Inherently Chiral Macrocyclic Oligothiophenes: Easily Accessible Electrosensitive Cavities with Outstanding Enantioselection Performances

2014 · Francesco Sannicolò, Patrizia R. Mussini, et al. · Chemistry - A European Journal · 5

Cover Picture: Inherently Chiral Macrocyclic Oligothiophenes: Easily Accessible Electrosensitive Cavities with Outstanding Enantioselection Performances (Chem. Eur. J. 47/2014)

2014 · Francesco Sannicolò, Patrizia R. Mussini, et al. · Chemistry - A European Journal

Works count: 5

Citation count: 96

H-index: 4

I10-index: 3