A novel attractive 1–3 interaction in trans-1,4-dichlorocyclohexane.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Conformational analysis of trans-1,4-dihalocyclohexanes
2. Conformational analysis of 1,4-disubstituted cyclohexanes. III. trans-1,4-Di(trifluoroacetoxy)cyclohexane
3. Equilibration of cis - and trans-2-t-butyl-4-hydroxycyclohexanone
4. Medium effects in rotational isomerism. VI. Inclusion of dipole-dipole interactions in polar solvents
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2. On the origin of the axial behaviour of 5-halomethyl groups in 1,3-dioxane. Evidence for non-bonded electrostatic attraction;Bulletin des Sociétés Chimiques Belges;2010-09-01
3. Hyperconjugation and the Increasing Bulk of OCOCX3 Substituents in Trans-1,4-Disubstituted Cyclohexanes Destabilize the Diequatorial Conformer;The Journal of Organic Chemistry;2006-05-11
4. The anomeric effect in substituted cyclohexanes. I. The role of hyperconjugative interactions and steric effect in monosubstituted cyclohexanes;Journal of Molecular Structure: THEOCHEM;2004-09
5. An FT-Raman Spectroscopic Study of the Conformational Behavior of trans-1,4-Dichlorocyclohexane Adsorbed in Zeolites;The Journal of Physical Chemistry B;2003-07-02
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