Vinyl Hydrogen Acidities of Two Stereoisomers
Author:
Affiliation:
1. Department of Chemistry, Stanford University, Stanford, California 94305-5080
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp0666075
Reference44 articles.
1. Intrinsic acidities of substituted phenols and benzoic acids determined by gas-phase proton-transfer equilibriums
2. Effects of the acidities of phenols from specific substituent-solvent interactions. Inherent substituent parameters from gas-phase acidities
3. Substituent and solvation effects on gas-phase acidities
4. Summary of gas phase acidity measurements involving acids AH. Entropy changes in proton transfer reactions involving negative ions. Bond dissociation energies D(A—H) and electron affinities EA(A)
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1. Electronic Effects of 11β Substituted 17β-Estradiol Derivatives and Instrumental Effects on the Relative Gas Phase Acidity;Journal of the American Society for Mass Spectrometry;2012-10-02
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