Stabilization of methyl anions by first row substituents
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference26 articles.
1. Molecular orbital theory of the electronic structure of molecules. 33. The effect of .alpha.-electropositive substituents on the stabilities of carbenium ions
2. Molecular orbital theory of the electronic structure of molecules. 35. .beta.-Substituent effects on the stabilities of ethyl and vinyl cations. Comparison with isoelectronic methyl boranes. The relative importance of hyperconjugative and inductive effects
3. Stabilization of methyl cations by second row substituents
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3. An Ab Initio Molecular Orbital Study of Sulfur-Substituted Carbanions: Toward an Understanding of Regiochemistry in the Chlorination of Unsymmetrical Sulfides;Australian Journal of Chemistry;1997
4. Structures and stabilization energies of methyl anions with main group substituents from the first five periods;Journal of Computational Chemistry;1994-06
5. Ab initio calculations on potential intermediates in metal reductions of carbonyl compounds. Stereochemical considerations;Journal of the American Chemical Society;1992-02
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