A theoretical study on the protonation of benzamide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Nuclear Magnetic Resonance Study of the Protolysis and Ionization of N-Methylacetamide1
2. Deuterium-Hydrogen Exchange in Amide N—H Groups1
3. The hammett acidity function and its non-applicability to amides
4. THE IONIZATION BEHAVIOR OF AMIDES IN CONCENTRATED SULFURIC ACIDS: II. APPLICATIONS OF THE HA FUNCTION TO RATES AND EQUILIBRIA
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1. Basicity of Very Weak Bases in 1,2-Dichloroethane;Chemistry - A European Journal;2016-10-21
2. Proton affinity and molecular basicity of m - and p -substituted benzamides in gas phase and in solution: A theoretical study;Chemical Physics Letters;2014-08
3. Dissociative Protonation and Proton Transfers: Fragmentation of α, β-Unsaturated Aromatic Ketones in Mass Spectrometry;The Journal of Organic Chemistry;2008-03-28
4. Dissociative Protonation Sites: Reactive Centers in Protonated Molecules Leading to Fragmentation in Mass Spectrometry;The Journal of Organic Chemistry;2006-06-22
5. Fragmentation of conjugated amides at the CC(O) bond in electrospray mass spectrometry: a proton-bound dimeric intermediate identified by the kinetic method;Rapid Communications in Mass Spectrometry;2004-05-27
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