Computational determination of the enthalpic and entropic contributions to the conformational preference of monosubstituted cyclohexanes. Molecular mechanics, semiempirical and density functional theory methods andab initiocalculations-Reference-Cited by-同舟云学术

Computational determination of the enthalpic and entropic contributions to the conformational preference of monosubstituted cyclohexanes. Molecular mechanics, semiempirical and density functional theory methods andab initiocalculations

Published:2002-11-21 Issue:12 Volume:15 Page:808-819
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Muñoz-Muñiz Omar,Juaristi Eusebio

Funder

Conacyt-Mexico

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference50 articles.

1. The conformation of the steroid nucleus

2. Neighboring Carbon and Hydrogen. XIX. t-Butylcyclohexyl Derivatives. Quantitative Conformational Analysis

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Site-Selective C(sp³)-H Chlorination Boosted by an Imidazolium-Functionalized Cage in Water;ACS Catalysis;2023-10-13

2. Studies on the formation of formaldehyde during 2-ethylhexyl 4-(dimethylamino)benzoate demethylation in the presence of reactive oxygen and chlorine species;Environmental Science and Pollution Research;2017-01-29

3. Looking for Treasure in Stereochemistry-Land. A Path Marked by Curiosity, Obstinacy, and Serendipity;The Journal of Organic Chemistry;2012-04-04

4. Unexpected coordination difference in geometric-isomerism between N,S- and N,N-heterocyclic carbenes in cyclometallated platinum(ii);Chemical Communications;2009

5. The anomeric effect in substituted cyclohexanes. II. The role of hyperconjugative interactions and steric effect in 1,4-disubstituted cyclohexanes;Journal of Molecular Structure: THEOCHEM;2005-03