Preparation of 1-pyridinylethanols of high enantiomeric purity by lipase catalysed transesterifications
✍ Scribed by Christian Orrenius; Anders Mattson; Torbjörn Norin; Niklas Öhrner; Karl Hult
- Book ID
- 103977065
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 304 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0957-4166
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📜 SIMILAR VOLUMES
13C NMR spectroscopy can be used for the quantitative analysis of mixtures of glycerides and the enantiomeric purity can be determined by using Eu(hfbc),-d reagent. This technique was applied to the study of the reaction mixture obtained from the transesterification of tributyrin catalysed by My-lip
Kinetic resolution of a series of racemic trans-cycloalkane-1,2-diol monoacetates rac-2a-d was performed by enantiomerically selective transesterification with vinyl acetate catalysed by commercial and our own-prepared fungal lipases to yield diacetates (R,R)-3a-d and monoacetates (S,S)-2a-d in high