New β-orcinol depsidones from Xanthoparmelia quintaria and a Thelotrema species

A new depsidone isolated from a new species of Thelotrema was identified as hyopstictic acid. Xanthoparmelia quintaria contains hypostictic and hyposalazinic acids.     

Eremophilane derivatives and other constituents from Senecio species

The investigation and reinvestigation respectively of 23 Senecio species afforded 11 further cacalol derivatives, a furoeremophilone, 17 eremophilanes, 4 bisabolene derivatives, a shikimic acid derivative, a bis-prenylated p-hydroxybenzaldehyde, menth-2-en- 1,7-diol and a cumol derivative. The configuration of some eremophilanes have been revised. Structures were elucidated by spectroscopic methods. The results are summarized in a table. The chemotaxonomic aspects agree with those of previous investigations.     

Ent-kauranes and other constituents of three Helianthus species

Aerial parts of Helianthus debilis subsp. cucumerifolius, H. occidentalis and H. simulans afforded a variety of known and some unknown ent-kauranoic acids. H. occidentalis gave, in addition, ciliaric acid and a new biogenetically related atisane derivative occidentalic acid. H. simulans gave the heliangolide leptocarpin and the flavone hymenoxin in addition to ent-kauranes. Several of the diterpenoids from these species inhibited larval growth of the sunflower moth.     

Free amino acids in the seeds of Acacia species

Free amino acids in the seeds of 80 species of Acacia have been determined. In addition to confirming the known difference in seed amino acid ‘patterns’ shown by species of the series Gummiferae on the one hand and species of the series Phyllodineae and Botryocephalae on the other, we have found that species of the series Vulgares Benth. show two additional ‘patterns’. One of these is common to some of the Afro-Asian species of the series which have been analysed and the other is common to species from America and Africa. One of the ‘marker’ amino acids of the Afro-Asian group is the neurotoxic lathyrogen α-amino-β-oxalylaminopropionic acid. The possible taxonomic and phylogenetic significance of these results is discussed, with special reference to five species A. albida, A. confusa, A. heterophylla, A. coulteri and A. kauaiensis.     

Triterpenoids from enkianthus campanulatus

From the leaves of Enkianthus campanulatus were isolated three new triterpenes, 3-oxo-19,23,24-trihydroxyurs-12-en-28-oic acid, 3β,6β, 19,23-tetrahydroxyurs-12-en-28-oic acid and 3β,6β,23-trihydroxyurs-12-en-28-oic acid.     

Sterols of three lichen species: Lobaria pulmonaria, Lobaria Scrobiculata and Usnea Longissima

Sterols were extracted from the lichens Lobaria pulmonaria, Lobaria scrobiculata and Usnea longissima with chloroform-methanol (2:1) (solvent-extractable fraction) followed by saponification of the residual lichen material to give a tightly-bound sterol fraction. The compounds were principally ergosterol, episterol, fecosterol and lichesterol with minor quantities of C₁₇, C₂₈ and C₂₉ monoenes and dienes of the phytosterol type.     

A novel abscisic acid metabolite from seeds of Robinia pseudacacia

Abscisic acid and its novel metabolise, which was a conjugated form of hydroxyabscisic acid (Metabolite C), were isolated from seeds of Robinia pseudacacia L. The structure of the conjugate was shown to be (+)-3-methyl-5 - [1(S),6(R) - 2,6 - dimethyl - 1 - hydroxy - 6 - (3 - hydroxy - 3 - methyl - 4 - carboxybutanoyloxymethyl) - 4 - oxo-cyclohex-2-enyl]-2-Z-4-E-pentadienoic acid and tentatively named β-hydroxy-β-methylglutarylhydroxyabscisic acid.     

Structure of histamine releasing guaianolides from Thapsia species

The structures of six hexaoxygenated guaianolides esterified with four non isomeric carboxylic acids have been established by ¹H NMR and ¹³C NMR spectroscopy. The acyl residues have been located by chemical ionisation mass spectrometry. Some of the acyl residues are novel for sesquiterpene lactones. The acyl residues in two additional guaianolides esterified with isomeric acids have been located by partial hydrolysis.     

Sapogenins from Guaiacum officinale

Acid hydrolysis of the saponins from the stem bark of Guaiacum officinale yielded the new sapogenin 3β,20η-dihydroxy-30-norolean-12-en-28-oic acid and the artifacts 3β-hydroxy-30-norolean-12,19-dien-28-oic acid and its methyl ester. Larreagenin, sitosterol and oleanolic acid were also isolated.     

Oxidative dimerization of ferulic acid by extracts from Sorghum

Extracts from leaves and first internodes of Sorghum bicolor catalyze the conversion of ferulic acid to a β-β-coupled dimer, the dilactone dimer of ferulic acid. The dilactone is then hydrolyzed, probably non-enzymatically, to a blue fluorescing compound, tentatively identified as a β-β-coupled dimer with at least one lactone ring opened to form a carboxylic acid. Both the initial enzymatic and the subsequent non-enzymatic steps are greater at pH 8 than pH 6. The most active preparation is a crude particulate fraction from leaves obtained by centrifugation at 37000 g; white light increases the amount of dimer formed.     

Isoflavanoid constituents from Dalbergia monetaria

The structures and isolation of eight compounds from Dalbergia monetaria seeds are described. Four of them are known rotenoids. In addition to a new isoflavone and its 7-β-D-glucoside, the first 12-dihydrorotenone, 12-dihydrodalbinol, and its 8′-β-D-glucoside were identified.     

Triterpenoid and phenolic constituents of Colubrina granulosa

Ether extracts of Colubrina granulosa heartwood yield the polyphenolic coumaranone maesopsin and 3 pentacyclic triterpene acids of the lup-20(29)-en-28-oic acid group, alphitolic, betulinic and ceanothic acids. Two new compounds, granulosic and colubrinic acids, which belong to a very small class of A ring contracted triterpenes were also isolated. The co-occurrence of maesopsin, alphitolic, betulinic and ceanothic acids suggests that C. granulosa (from Panama) may be closely related or identical to the Australian species, Alphitonia whitei, in which these relatively rare compounds also occur.     

Sesquiterpenoid and acetylenic constituents of seven Clibadium species

The investigation of seven Clibadium species resulted in the isolation of a new germacrolide from C. surinamense, trans-β-bergamotene, a new sesquiterpene from C. asperum and a new C-17 acetylenic alcohol from C. glomeratum. Five known acetylenic compounds were present in some members of the genus. In good agreement with morphological data, the presence of ichthyothereol and its acetate in several members of Clibadium suggest affiliation with the genus Ichthyothere within the subtribe Milleriinae (Heliantheae-Compositae).     

Alkaloid and lignan constituents of Cinnamosma madagascariensis

A new lignan glycoside, 5-methoxy-9-β-xylopyranosyl-(-)- isolariciresinol and two indole alkaloids have been characterised from the bark of Cinnamosma madagascariensis.     

Diterpene acids from Helianthus species and their microbiological conversion by Gibberella fujikuroi, mutant B1-41a

The diterpene acid content in 10 species of Helianthus has been investigated. Ent-12,16-cyclokauranoic acid, isolated from H. annuus, is converted into a series of 12,16-cyclogibberellins by cultures of Gibberella fujikuroi, mutant B1-41a, and 12,16-cyclogibberellins A₉, and A₁₂ have been isolated. Ent-12β-acetoxykaurenoic acid and ent-13(S)-angeloxyatisenoic acid have been isolated from H. decapetalus; the metabolism of ent-13(S)-hydroxyatisenoic acid and atisenoic acid by B1-41a is also described.     

Flavonoids from the seeds of Lonchocarpus costaricensis

Seven flavonoids have been isolated from the seeds of Lonchocarpus costaricensis of which four appear to be novel. The new compounds have been identified as the β-hydroxychalcone demethylpraecansone-B and the flavanones 7-(3,3-dimethylallyloxy)-8-(3-hydroxy-3-methyl-trans-but-1-enyl)flavanone, 7-(3,3-dimethylallyloxy)-8-(3,3-dimethylallyl)-5-methoxyflavanone and 8-(3,3-dimethylallyl)-5,7-dimethoxyflavanone.