The absolute configuration of ( - )-angolensin
- 1 January 1965
- journal article
- research article
- Published by CSIRO Publishing in Australian Journal of Chemistry
- Vol. 18 (11) , 1787-1790
- https://doi.org/10.1071/ch9651787
Abstract
Oxidation of (-)-angolensin isolated from the heartwood of Pterocarpus angolensis has yielded (-)-2-(4-methoxyphenyl)propionic acid (Ia). This establishes that the isoflavonoid, (-)-angolensin, has the R-configuration (II) and the relation between this absolute stereochemistry and that of other isoflavonoids is discussed.Keywords
This publication has 2 references indexed in Scilit:
- The neoflavanoid group of natural products—II.Tetrahedron, 1965
- The absolute configurations of ( - )-angolensin and some related 1,2-diarylpropanesAustralian Journal of Chemistry, 1965