Conformational properties of trans-2-halo-acetoxycyclohexanes: 1H NMR, solvation and theoretical investigation
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry
Reference31 articles.
1. Halogenated six-membered rings: a theoretical approach for substituent effects in conformational analysis
2. Interaction in trans-2-halocyclohexanols — an infrared and theoretical study
3. Conformational analysis oftrans-2-halocyclohexanols and their methyl ethers: a1H NMR, theoretical and solvation approach
4. Conformers and Intramolecular Hydrogen Bond oftrans-2-Halocyclohexanols
5. Application of 13C nuclear magnetic resonance to the conformational analysis of vicinally di- and trisubstituted cyclohexanes: halohydrins, methoxyhalohydrins, and their acetates
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3. Experimental and Theoretical Studies of Intramolecular Hydrogen Bonding in 3-Hydroxytetrahydropyran: Beyond AIM Analysis;The Journal of Physical Chemistry A;2014-04-08
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