Synthesis and NMR spectroscopic conformational analysis of esters of 4-hydroxy-cyclohexanone - The more polar the molecule the more stable the axial conformer

Tetrahedron

Volumn 68, Issue 10, 2012, Pages 2363-2373

  Kleinpeter, Erich ^a   Heydenreich, Matthias ^a   Koch, Andreas ^a   Linker, Torsten ^a  

^a UNIVERSITY OF POTSDAM   (Germany)

Author keywords

4 Substituted cyclohexanones; ALTONA equation; Conformational analysis; Dynamic NMR; Quantum chemical calculations; Simulation of 1H NMR spectra

Indexed keywords

4 HYDROXYCYCLOHEXANONE; CARBOXYLIC ACID; CYCLOHEXANONE DERIVATIVE; ESTER; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CIS ISOMER; CONFORMATION; DENSITY FUNCTIONAL THEORY; ELECTROCHEMISTRY; MOLECULAR STABILITY; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOSPECIFICITY; SYNTHESIS; TEMPERATURE; TRANS ISOMER;

EID: 84857047837     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.01.022     Document Type: Article

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