Conformational Spaces and Absolute Configurations of Chiral Fluorinated Inhalation Anaesthetics. A Theoretical Study
- 1 May 1999
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 64 (11) , 3878-3884
- https://doi.org/10.1021/jo9821325
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Ab initio calculation of atomic axial tensors and vibrational rotational strengths using density functional theoryMolecular Physics, 1996
- Absolute Configurations of the Inhalation Anesthetics Isoflurane and DesfluraneAngewandte Chemie International Edition in English, 1996
- Vibrational Optical ActivityApplied Spectroscopy, 1996
- The potencies of optically active anaestheticsEuropean Journal of Medicinal Chemistry, 1995
- Asymmetric Synthesis of the Volatile Anesthetic 1,2,2,2-Tetrafluoroethyl Chlorofluoromethyl Ether Using a Stereospecific Decarboxylation of Unusual Stereochemical OutcomeThe Journal of Organic Chemistry, 1995
- Enantiomer separation of chiral inhalation anesthetics (enflurane, isoflurane and desflurane) by gas chromatography on a γ‐cyclodextrin derivativeRecueil des Travaux Chimiques des Pays-Bas, 1995
- The potential for safer anaesthesia using stereoselective anaestheticsTrends in Pharmacological Sciences, 1994
- Molecular and cellular mechanisms of general anaesthesiaNature, 1994
- Determination of Absolute Configurations and Predominant Conformations of General Inhalation Anesthetics: DesfluraneJournal of Pharmaceutical Sciences, 1993
- Stereospecific Effects of Inhalational General Anesthetic Optical Isomers on Nerve Ion ChannelsScience, 1991