The case of intramolecular hydrogen bonding, hyperconjugation and classical effects on the conformational isomerism of substituted carbonyl and thiocarbonyl compounds-Reference-Cited by-同舟云学术

The case of intramolecular hydrogen bonding, hyperconjugation and classical effects on the conformational isomerism of substituted carbonyl and thiocarbonyl compounds

Published:2008-02 Issue:1-3 Volume:851 Page:147-157
ISSN:0166-1280
Container-title:Journal of Molecular Structure: THEOCHEM
language:en
Short-container-title:Journal of Molecular Structure: THEOCHEM

Author:

Ducati Lucas C.,Freitas Matheus P.,Tormena Cláudio F.,Rittner Roberto

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry

Reference22 articles.

1. Ueber die geometrischen Isomerien der Hexamethylenderivate

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4. Hyperconjugation not steric repulsion leads to the staggered structure of ethane

5. The Case for Steric Repulsion Causing the Staggered Conformation of Ethane

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