Diligustilide: Enantiomeric Derivatives, Absolute Configuration and Cytotoxic Properties
نویسندگان
چکیده
منابع مشابه
NMR chemical shifts to determine the absolute configuration and enantiomeric purity for enantiomers of 3,3 -disubstituted-MeO-BIPHEP derivatives
The absolute configuration of a series of 3,3'-disubstituted-MeO-BIPHEP derivatives can be determined by the 'H NMR chemical shift of the methoxyl group when the 3,3'-disubsituted-MeO-BIPHEP derivative is mixed with (-)-(2fl,3/?)-dibenzoyltartaric acid ((-)-DBTA) (1:2) and its NMR spectrum is run in CDC1,. The chemical shift of the methoxyl group in the 5'ax enantiomer always occurred at higher...
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ژورنال
عنوان ژورنال: Journal of the Mexican Chemical Society
سال: 2017
ISSN: 2594-0317,1870-249X
DOI: 10.29356/jmcs.v56i2.326