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פותח על ידי קלירמאש פתרונות בע"מ -
Lipase-catalyzed resolution of acyclic amino alcohol precursors
Year:
1990
Source of publication :
Journal of Organic Chemistry
Authors :
הניג, הלמוט
;
.
Volume :
55
Co-Authors:
Foelsche, E., Institute of Organic Chemistry, Graz University of Technology, A-8010 Graz, Austria
Hickel, A., Institute of Organic Chemistry, Graz University of Technology, A-8010 Graz, Austria
Hönig, 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:
1749
To page:
1753
(
Total pages:
5
)
Abstract:
Lipase-catalyzed resolution of acyclic 2-azido alcohols as precursors for amino alcohols was readily accomplished. Butanoates of racemic acyclic azidoalkanols were hydrolyzed by using commercially available lipases from Candida cylindracea and Pseudomonas fluorescens, respectively. Some representative examples of acyclic secondary 2-azido alcohols have been obtained with enantiomeric excess ranging from 24 to >98%. © 1990 American Chemical Society.
Note:
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DOI :
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Affiliations:
Database:
סקופוס
Publication Type:
מאמר
;
.
Language:
אנגלית
Editors' remarks:
ID:
24952
Last updated date:
02/03/2022 17:27
Creation date:
17/04/2018 00:11
Scientific Publication
Lipase-catalyzed resolution of acyclic amino alcohol precursors
55
Foelsche, E., Institute of Organic Chemistry, Graz University of Technology, A-8010 Graz, Austria
Hickel, A., Institute of Organic Chemistry, Graz University of Technology, A-8010 Graz, Austria
Hönig, 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
Lipase-catalyzed resolution of acyclic amino alcohol precursors
Lipase-catalyzed resolution of acyclic 2-azido alcohols as precursors for amino alcohols was readily accomplished. Butanoates of racemic acyclic azidoalkanols were hydrolyzed by using commercially available lipases from Candida cylindracea and Pseudomonas fluorescens, respectively. Some representative examples of acyclic secondary 2-azido alcohols have been obtained with enantiomeric excess ranging from 24 to >98%. © 1990 American Chemical Society.
Scientific Publication
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