Modulation of Conformational Preferences of Heteroaromatic Ethers and Amides through Protonation and Ionization: Charge Effect-Reference-Cited by-同舟云学术

Modulation of Conformational Preferences of Heteroaromatic Ethers and Amides through Protonation and Ionization: Charge Effect

Published:2019-06-11 Issue:7 Volume:8 Page:840-851
ISSN:2191-1363
Container-title:ChemistryOpen
language:en
Short-container-title:ChemistryOpen

Author:

Dai Wenshuai¹²,Zhang Zhe¹²,Du Yikui¹^ORCID

Affiliation:

1. Beijing National Laboratory of Molecular Science, State Key laboratory of Molecular Reaction DynamicsInstitute of Chemistry, Chinese Academy of Sciences Beijing 100190 Beijing PR China

2. School of Chemical EngineeringUniversity of Chinese Academy of Sciences Beijing 100049 P. R. China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/open.201900103

Reference48 articles.

1. A new twist on molecular shape

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

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

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

5. Computational evidence that hyperconjugative interactions are not responsible for the anomeric effect

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