Kinetic resolution of heptan-2-ol-enantiomers by lipase-catalysed esteriîication in organic solvent

Karl Heinz Engel; Martina Bohnen; Roland Tressl

doi:10.1007/BF01042739

Kinetic resolution of heptan-2-ol-enantiomers by lipase-catalysed esteriîication in organic solvent

Karl Heinz Engel
, Martina Bohnen
, Roland Tressl

Technische Universität Berlin

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

Abstract

The lipase-catalysed esterification of racemic heptan-2-ol in organic solvent has been investigated. Porcine pancreas lipase, suspended in heptane, preferentially catalyses the synthesis of (R)-2heptyl butyrate starting from (R,S)-heptan-2-ol and butyric acid. The distribution of the reaction products and the stereochemical course of the esterification have been investigated by means of capillary gas chromatographic methods.

Original language	English
Pages (from-to)	144-147
Number of pages	4
Journal	Zeitschrift fur Lebensmittel -Untersuchung und -Forschung
Volume	188
Issue number	2
DOIs	https://doi.org/10.1007/BF01042739
State	Published - Feb 1989
Externally published	Yes

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title = "Kinetic resolution of heptan-2-ol-enantiomers by lipase-catalysed esteri{\^i}ication in organic solvent",

abstract = "The lipase-catalysed esterification of racemic heptan-2-ol in organic solvent has been investigated. Porcine pancreas lipase, suspended in heptane, preferentially catalyses the synthesis of (R)-2heptyl butyrate starting from (R,S)-heptan-2-ol and butyric acid. The distribution of the reaction products and the stereochemical course of the esterification have been investigated by means of capillary gas chromatographic methods.",

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year = "1989",

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doi = "10.1007/BF01042739",

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pages = "144--147",

journal = "Zeitschrift fur Lebensmittel -Untersuchung und -Forschung",

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number = "2",

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T1 - Kinetic resolution of heptan-2-ol-enantiomers by lipase-catalysed esteriîication in organic solvent

AU - Engel, Karl Heinz

AU - Bohnen, Martina

AU - Tressl, Roland

PY - 1989/2

Y1 - 1989/2

N2 - The lipase-catalysed esterification of racemic heptan-2-ol in organic solvent has been investigated. Porcine pancreas lipase, suspended in heptane, preferentially catalyses the synthesis of (R)-2heptyl butyrate starting from (R,S)-heptan-2-ol and butyric acid. The distribution of the reaction products and the stereochemical course of the esterification have been investigated by means of capillary gas chromatographic methods.

AB - The lipase-catalysed esterification of racemic heptan-2-ol in organic solvent has been investigated. Porcine pancreas lipase, suspended in heptane, preferentially catalyses the synthesis of (R)-2heptyl butyrate starting from (R,S)-heptan-2-ol and butyric acid. The distribution of the reaction products and the stereochemical course of the esterification have been investigated by means of capillary gas chromatographic methods.

UR - https://www.scopus.com/pages/publications/34249976152

U2 - 10.1007/BF01042739

DO - 10.1007/BF01042739

M3 - Article

AN - SCOPUS:34249976152

SN - 0044-3026

VL - 188

SP - 144

EP - 147

JO - Zeitschrift fur Lebensmittel -Untersuchung und -Forschung

JF - Zeitschrift fur Lebensmittel -Untersuchung und -Forschung

IS - 2

ER -

Kinetic resolution of heptan-2-ol-enantiomers by lipase-catalysed esteriîication in organic solvent

Abstract

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