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A general method for the separation of enantiomeric trans-2-substituted cyclohexanols
Year:
1990
Source of publication :
Synthesis
Authors :
Hönig, Helmut
;
.
Volume :
Co-Authors:
Honig, H., Institute of Organic Chemistry, Graz University of Technology, A-8010 Graz, Austria
Seufer-Wasserthal, P., Institute of Organic Chemistry, Graz University of Technology, A-8010 Graz, Austria
Facilitators :
From page:
1137
To page:
1140
(
Total pages:
4
)
Abstract:
An number of different racemic trans-2-substituted cyclohexanols has been prepared in high optical purity by optical resolution of the respective 2'-substituted cyclohexyl butanoates with the aid of commercially available lipases.
Note:
Related Files :
article
chemical structure
cyclohexanol
cyclohexanol derivative
nuclear magnetic resonance
Synthesis
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Related Content
More details
DOI :
Article number:
Affiliations:
Database:
Scopus
Publication Type:
article
;
.
Language:
English
Editors' remarks:
ID:
27365
Last updated date:
02/03/2022 17:27
Creation date:
17/04/2018 00:30
Scientific Publication
A general method for the separation of enantiomeric trans-2-substituted cyclohexanols
Honig, H., Institute of Organic Chemistry, Graz University of Technology, A-8010 Graz, Austria
Seufer-Wasserthal, P., Institute of Organic Chemistry, Graz University of Technology, A-8010 Graz, Austria
A general method for the separation of enantiomeric trans-2-substituted cyclohexanols
An number of different racemic trans-2-substituted cyclohexanols has been prepared in high optical purity by optical resolution of the respective 2'-substituted cyclohexyl butanoates with the aid of commercially available lipases.
Scientific Publication
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