Chiroptical properties of S-alkyl derivatives of 1-thioglycerol
✍ Scribed by Peter Michelsen; Bengt Herslöf; Björn Åkesson
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 550 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0009-3084
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✦ Synopsis
Several racemic and optically active S-alkyl derivatives of l-thioglycerol have been synthesized. From 3-S-tetradecyl-3-thio-sn-glycerol the dioleoyl and diacetyl esters were prepared. 1,2-Dioleoyl-3-S-tetradecyl-3-thio-sn-glycerol was converted into the corresponding sulphoxide and sulphone. The ehiroptical properties of these compounds were investigated by ORD and CD. Such measurements can be used in studies on the metabolism of enantiomeric acyiglycerols.
📜 SIMILAR VOLUMES
## Abstract The chiroptical properties of S‐proline conformational isomers are examined on a theoretical model in which electronic wave functions are obtained from semiempirical molecular orbital calculations. The CNDO/S molecular orbital model is used to perform SCF‐MO calculations on ground state