Stereoelectronic Interaction and Their Effects on Conformational Preference for 2-Substituted Methylenecyclohexane: An Experimental and Theoretical Investigation
Author:
Affiliation:
1. Department of Organic Chemistry, Chemistry Institute, University of Campinas-UNICAMP-CEP, P. O. Box 6154, 13084-971 Campinas, SP, Brazil
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp8048636
Reference41 articles.
1. Interaction in trans-2-halocyclohexanols — an infrared and theoretical study
2. Halogenated six-membered rings: a theoretical approach for substituent effects in conformational analysis
3. Substituent interactions in trans-2-substituted methoxycyclohexanes: an explanation to the conformational behaviour in a chemometric and theoretical view
4. Conformational analysis oftrans-2-halocyclohexanols and their methyl ethers: a1H NMR, theoretical and solvation approach
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