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Schmitt, B. et al.

Phenylpropanoid interconversion in Anigozanthos preissii observed by high-performance liquid chromatography-nuclear magnetic resonance spectroscopy.

HPLC-NMR spectroscopy was employed to observe isotopically labelled intermediates of the phenylpropanoid metabolism in Anigozanthos preissii. Hydroxylation of dihydrocinnamic acid to dihydro-p-coumaric acid and the reversible interconversion between phenylpropanoids and phenylpropenoids were detected, suggesting the operation of a metabolic network in early phenylpropanoid biosynthesis in this plant.[1]

References

Phenylpropanoid interconversion in Anigozanthos preissii observed by high-performance liquid chromatography-nuclear magnetic resonance spectroscopy. Schmitt, B., Schneider, B. Phytochemical analysis : PCA. (2001) [Pubmed]

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