Alkyl Substituent Effect in the Deprotonation of Unsymmetrical Ketones
Author:
Affiliation:
1. Department of Chemistry, Stanford University, Stanford, California 94305-5080
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry,General Engineering
Link
https://pubs.acs.org/doi/pdf/10.1021/jp953249p
Reference28 articles.
1. Regio-specifity of the deprotonation of some aliphatic ketones and sulfones by NCl
2. The mechanism of directed second lithiations: detection of short proton-lithium separations by 6Li-1H HOESY (2D-heteronuclear Overhauser spectroscopy)
3. Stereochemical Criteria Providing Unambiguous Experimental Evidence for the intermediacy of ion/molecule complexes in the generation of enolates from gaseous alkoxides. Short communication
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1. ChemInform Abstract: Alkyl Substituent Effect in the Deprotonation of Unsymmetrical Ketones;ChemInform;2010-08-05
2. The synthesis and characterisation of multi-labelled [D,13C] 2-deuterio-2-methyl aromatic ketones;Journal of Labelled Compounds and Radiopharmaceuticals;2003
3. A Succinct Route to the Synthesis of Multi-Labelled [D,13C]α-Methyl Aromatic Ketones;Bulletin of the Chemical Society of Japan;2002-05
4. C−H···Carboxylate Oxygen Hydrogen Bonding in Substrate Activation by Acyl-CoA Dehydrogenases: Synergy between the H-bonds;The Journal of Physical Chemistry B;2002-03-20
5. Energetics and Mechanism of Alkyl Cleavage Transition States: Relative Gas-Phase Acidities of Alkanes;Journal of the American Chemical Society;2000-10-21
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