A design to prevent floating within the N scale of nucleophilicity
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference42 articles.
1. Quantitative Correlation of Relative Rates. Comparison of Hydroxide Ion with Other Nucleophilic Reagents toward Alkyl Halides, Esters, Epoxides and Acyl Halides1
2. Correlation of Solvolysis Rates. VIII. Benzhydryl Chloride and Bromide. Comparison of mY and Swain's Correlations1
3. Sixty Years of the Grunwald–Winstein Equation: Development and Recent Applications
4. Nucleophilicity towards a saturated carbon atom: rate constants for the aminolysis of methyl 4-nitrobenzenesulfonate in aqueous solution. A comparison of the n and N + parameters for amine nucleophilicity
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1. Intrinsic relative nucleophilicity of indoles;Theoretical Chemistry Accounts;2016-08
2. Positioning solvolyses within the SN2-SN1 and SN3-SN2 spectrum of reaction mechanisms;Journal of Physical Organic Chemistry;2016-06-01
3. Effect of microheterogeneity of CF3 CH2 OH-H2 O mixed solvent on reactions of carbocations from 1,2,2,3-tetramethyl-1,2-dihydroquinoline;Journal of Physical Organic Chemistry;2013-05-23
4. A comprehensive N + scale of nucleophilicity in an equation including a Swain-Scott response/selectivity parameter;Journal of Physical Organic Chemistry;2012-12-11
5. Nucleophilic Aliphatic Substitution;Organic Reaction Mechanisms Series;2012-12-04
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