Application of enantioselective capillary gas chromatography in lipase-catalysed transesterification reactions in organic media

Research output: Contribution to journalArticleResearchpeer review

Authors

  • U. Bornscheuer
  • S. Schapöhler
  • Th Scheper
  • K. Schügerl
  • W. A. König

Research Organisations

External Research Organisations

  • Universität Hamburg
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Details

Original languageEnglish
Pages (from-to)288-290
Number of pages3
JournalJournal of Chromatography A
Volume606
Issue number2
Publication statusPublished - 14 Aug 1992

Abstract

The analysis of enantiomeric excesses of substrate and product during an enantioselective reaction can be performed easily with a chiral stationary phase based on γ-cyclodextrin. The transesterification of six related allylic alcohols to their corresponding acetates was catalysed by lipase from Pseudomonas cepacia.

ASJC Scopus subject areas

Cite this

Application of enantioselective capillary gas chromatography in lipase-catalysed transesterification reactions in organic media. / Bornscheuer, U.; Schapöhler, S.; Scheper, Th et al.
In: Journal of Chromatography A, Vol. 606, No. 2, 14.08.1992, p. 288-290.

Research output: Contribution to journalArticleResearchpeer review

Bornscheuer U, Schapöhler S, Scheper T, Schügerl K, König WA. Application of enantioselective capillary gas chromatography in lipase-catalysed transesterification reactions in organic media. Journal of Chromatography A. 1992 Aug 14;606(2):288-290. doi: 10.1016/0021-9673(92)87040-F
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