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The known isoflavones, genistein, 5- O -methylgenistein, wighteone, luteone and alpinumisoflavone, have been isolated from methanol extracts of Laburnum anagyroides pods. The pod extracts also yielded three new isoflavones; anagyroidisoflavone A (5,4′-dihydroxy-(3″,4″-dihydro-3″-hydroxy-4″-methoxy)-2″,2″-dimethylpyrano (5″,6″:6,7)isoflavone), anagyroidisoflavone B (5,4′-dihydroxy-(3″,4″-dihydro-3″,4″-epoxy)-2″,2″-dimethylpyrano (5″,6″:6,7)isoflavone) and laburnetin (5,7,4′-trihydroxy-6-(2″-hydroxy-3″-methyl-3″-butenyl)isoflavone). The structures of the new compounds were determined by spectral analyses.

The monomeric composition of the suberins from 16 species of higher plants was determined by chromatographic methods following depolymerization of the isolated extractive-free cork layers with sodium methoxide-methanol. 1-Alkanols (mainly C18C28), alkanoic (mainly C16C30), α,ω-alkanedioic (mainly C16C24), ω-hydroxyalkanoic (mainly C16C21), dihydroxyhexadecanoic (mainly 10,16-dihydroxy- and 16-dihydroxyhexadecanoic), monohydroxyepoxyalkanoic (9,10-epoxy-18-hydroxyoctadecanoic), trihydroxyalkanoic (9,10, 18-trihydroxyoctadecanoic), epoxyalkanedioic (9,10-epoxyoctadecane-1,18-dioic) and dihydroxyalkanedioic (9,10-dihydroxyoctadecane-1 18-dioic) acids were detected in all species. The suberins differed from one another mainly in the relative proportions of these monomer classes and in the homologue content of their 1-alkanol, alkanoic, α,ω-alkanedioic and ω-hydroxyalkanoic acid fractions. C18 epoxy and vic-diol monomers were major components (32–59%) of half of the suberins examined (Quercus robur, Q. ilex, Q. suber, Fagus sylvatica, Castanea sativa, Betula pendula, Acer griseum, Fraxinus excelsior) where as ω-hydroxyalkanoic and α,ω-alkanedioic acids predominated in those that contained smaller quantities of such polar C18 monomers (Acer pseudoplatanus, Ribes nigrum, Euonymus alatus, Populus tremula, Solanum tuberosum, Sambucus nigra, Laburnum anagyroides, Cupressus leylandii). All species, however, contained substantial amounts (14–55 %) of ω-hydroxyalkanoic acids, the most common homologues being 18:1 (9) and 22: 0. The dominant α,ω-alkanedioic acid homologues were 16: 0 and 18: 1 (9) whereas 22: 0, 24: 0 and 26: 0, and 20: 0, 22: 0 and 24: 0 were usually the principal homologues in the 1-alkanol and alkanoic acid fractions, respectively. The most diagnostic feature of the suberins examined was the presence of monomers greater than C18 in chain length; most of the C16 and C18 monomers identified in the suberins also occur in plant cutins emphasizing the close chemical similarity between the two anatomical groups of lipid biopolymer.

A new type of higher plant alkaloid, 3-hydroxy-11-norcytisine, was isolated from the green pods of Laburnum anagyroides and characterized spectroscopically as its dansyl derivative.