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Nucleophilic vinylic substitution. A single- or a multi-step process?
National licenceAmerican Chemical Society | 1981| -
The rapid steps in nucleophilic vinylic addition-elimination substitution. Recent developments
National licenceAmerican Chemical Society | 1992| -
Recent Advances in Our Mechanistic Understanding of SNV Reactions
American Chemical Society | 2009| -
A Rich Array of Reactions of Cyanomonothiocarbonylmalonamides RNHCSCH(CN)CONHR‘ and Their Thioenols RNHC(SH)C(CN)CONHR‘1
American Chemical Society | 2008| -
Oxa-ene Reaction of Enols of Amides with 4-Phenyl-1,2,4-triazoline-3,5-dione †
American Chemical Society | 2008| -
Enols and thioenols of substituted cyanomonothiocarbonylmalonamides: structures, enolization vs. thioenolization, equilibria and conformations
National licenceRoyal Society of Chemistry | 2008| -
Unequivocal SRN1 Route of Vinyl Halides with a Multitude of Competing Pathways: Reactivity and Structure of the Vinyl Radical Intermediate
American Chemical Society | 2003| -
Stable simple enols. 17. Linear free energy relationship between keto .dblharw. enol equilibrium constants of stable .beta.,.beta.-dimesityl and unstable .beta.,.beta.-unsubstituted .alpha.-substituted enols
National licenceAmerican Chemical Society | 1987| -
Enols of Amides Activated by the 2,2,2-Trichloroethoxycarbonyl Group
American Chemical Society | 2004| -
Vinylic cations from solvolysis. Part 40. On the distribution of products in the degenerate rearrangement of doubly-labeled triarylvinyl cations
National licenceAmerican Chemical Society | 1984| -
Stable Simple Enols. Self-Catalyzed E/Z-Isomerization of the Sterically Crowded 2-(m-Methoxymesityl)-1,2-dimesitylethenol1
American Chemical Society | 2003|
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