Formononetin and biochanin A 7-O-glucosides (1a and 2a) and their malonate hemi-ester derivatives (1b and 2b) have been isolated from red clover and from the Yarloop strain of subterranean clover. Structure (2b) is a correction of an earlier structural assignment to this compound. Small amounts of the derived methyl esters (1c and 2c) are also present in both clovers. Similar derivatives of genistein have been obtained from the Yarloop strain, although only the 7-O-glucoside (3a) has been isolated in pure form. Studies on red clover and on nine strains of subterranean clover have demonstrated in all cases that the acidic malonate esters account for the predominant proportion of the glycosides.

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Ethanol extracts of Ervatamia orientalis have yielded the following known alkaloids: ibogaine, iboxygaine, voacristine, vobasine, dregamine, tabernaemontanine, apparicine, voacamine and 16- demethoxycarbonylvoacamine. In addition, two new dimeric alkaloids of the voacamine group and the novel 2-acylindoles ervatamine, 20- epiervatamine and 19-dehydroervatamine have been isolated from the extracts. The two new dimeric compounds have been identified by physical and chemical methods as 16-demethoxycarbonyldihydrovoacamine and 16-demethoxycarbonyl-20?-epi-dihydrovoacamine.

A pigment from Eremophila fraseri F. Muell. has been shown to be 5,3',5'-trihydroxy-3,6,7,4'-tetramethoxyflavone by degradation and synthesis of the 3',5'-dimethyl ether. Pinobanksin and galangin-3-methyl ether have been isolated from E. ramossissima and E. alternifolia.

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