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Microbial hydroxylation of 2-cycloalkylbenzoxazoles. Part III. Determination of product enantiomeric excess and cleavage of benzoxazoles

✍ 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
103977410
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
327 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.