The anomeric effect in substituted cyclohexanes. II. The role of hyperconjugative interactions and steric effect in 1,4-disubstituted cyclohexanes-Reference-Cited by-同舟云学术

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The anomeric effect in substituted cyclohexanes. II. The role of hyperconjugative interactions and steric effect in 1,4-disubstituted cyclohexanes

Published:2005-03 Issue:1-3 Volume:718 Page:141-151
ISSN:0166-1280
Container-title:Journal of Molecular Structure: THEOCHEM
language:en
Short-container-title:Journal of Molecular Structure: THEOCHEM

Author:

Taddei Ferdinando,Kleinpeter Erich

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry

Reference44 articles.

1. Stereochemistry of Organic Compounds;Eliel,1994

2. Stereodynamics of cyclohexane and substituted cyclohexanes. Substituent A values;Bushweller,1995

3. Conformational Analysis;Eliel,1965

4. Table of Conformational Energies-1967

5. Advanced Organic Chemistry;March,1985

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1. The conformational behavior and structure of monosubstituted-1,3,5-trisilacyclohexanes: 1-N,N-dimethylamino-1,3,5-trisilacyclohexane;Journal of Molecular Structure;2021-01

2. Conformational rivalry of geminal substituents in silacyclohexane derivatives: 1-Phenyl vs. 1-OR, R=H or Me;Tetrahedron;2019-05

3. Strong hyperconjugative interactions limit solvent and substituent influence on conformational equilibrium: the case of cis-2-halocyclohexylamines;Beilstein Journal of Organic Chemistry;2019-04-01

4. Polymorphism of 1,3-cyclohexanediols: molecular structure and plastic crystal formation of cyclohexanediol isomers;CrystEngComm;2019

5. Hyperconjugation;WIREs Computational Molecular Science;2018-09-06

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