The calculation of strain energies in cyclic and polycyclic hydrocarbons by the maximum overlap approximation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Evaluation of strain in hydrocarbons. The strain in adamantane and its origin
2. Critical evaluation of molecular mechanics
3. Hybridization by the maximum overlap method
4. Comparative study of hybridization in hydrocarbons
5. Hybridization in 2,5-dimethyl-7,7-dicyanonorcaradiene by the maximum overlap approximation
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1. Estimating Ring Strain Energies of Highly Substituted Cyclohexanes with the Semi-homodesmotic Approach: Why Substantial Ring Strain Exists for Nominally Tetrahedral Ring Carbon Atoms;The Journal of Organic Chemistry;2015-09-29
2. Antiaromaticity and Aromaticity in Carbocyclic Four-Membered Rings;PATAI'S Chemistry of Functional Groups;2009-12-15
3. The Baeyer strain is strongly affected by the nucleus–electron attraction—a comment on the Letter of G. Hohlneicher and L. Packschies [Tetrahedron Lett. 2007, 48, 6429–6433];Tetrahedron Letters;2008-02
4. On the origin of Baeyer strain in molecules – an ab initio and DFT analysis;Theoretical Chemistry Accounts;2005-05-30
5. Dominant Role of the π Framework in Cyclobutadiene;The Journal of Physical Chemistry A;2004-09-25
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