Absolute stereochemistry of guaianolides, of matricin and its epimers, of yarrow proazulenes, and of chamazulene carboxylic acid

Known determinations of the absolute configuration of guaianolides were collected and found to be few. The absolute configurations of guaianolides rest on the assumption that 7‐H always has α‐orientation. For matricin, only the relative configuration was determined. On the basis of a detailed study...

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Veröffentlicht in:	Chirality (New York, N.Y.) N.Y.), 2001, Vol.13 (7), p.337-341
Hauptverfasser:	Imming, Peter, Goeters, Susanne, Pawlitzki, Gregor, Hempel, Bernd
Format:	Artikel
Sprache:	eng
Schlagworte:	absolute configuration Anti-Inflammatory Agents, Non-Steroidal - chemistry Asteraceae - chemistry Azulenes Carboxylic Acids - chemistry Circular Dichroism Cycloheptanes - chemistry ibuprofen Lactones Magnetic Resonance Spectroscopy - methods naproxen NMR sesquiterpene lactones Sesquiterpenes - chemistry Stereoisomerism
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