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Microbial hydroxylation of 2-cycloalkylbenoxazoles. Part II. Determination of product structures and enhancement of enantiomeric excess

✍ Scribed by A. de Raadt; H. Griengl; M. Petsch; P. Plachota; N. Schoo; H. Weber; G. Braunegg; I. Kopper; M. Kreiner; A. Zeiser

Book ID
103977409
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
1004 KB
Volume
7
Category
Article
ISSN
0957-4166

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## Abstract Capillary GC on permethyl α‐, β‐, and γ‐cyclodextrins has been applied to separate and quantify the enantiomers of some 2,3‐iso‐propylidene‐1,2,3‐cyclohexanetriol derivatives. Quantitative CGC data are compared to those obtained with chiral shift ^1^H NMR.