Abstract
The structure of the methyl ester derivative (2) of ent-20-hydroxy-16betaH-kaurane-17,19-dioic acid 19,20-lactone has been determined by X-ray crystallographic methods. The delta-lactone ring adopts the chair conformation both in the solid state and in solution.
Original language | English |
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Pages (from-to) | 743-747 |
Journal | Australian Journal of Chemistry: an international journal for chemical science |
Volume | 46 |
DOIs | |
Publication status | Published - 1993 |