Flavour and Fragrance Journal · 2003 · 36 citations · 13 references
BiologyBiosynthesisEngineeringBiochemistryNatural SciencesEndophyte ResearchSecondary MetaboliteVolatile Hydrolysis ProductsPhytopharmacologyPhytochemicalFarsetia Aegyptia VarNatural AutolysisPhytochemistryPharmacologyGc–ms AnalysisPlant Physiology
Abstract Twenty‐two volatile glucosinolate hydrolysis products from seeds and leaves of Farsetia aegyptia var. ovalis were identified and quantified using both natural autolysis and exogenous myrosinase, followed by GC–MS. The 22 isothiocyanate thiocyanate, epithioalkane nitrile and nitrile hydrolysis products identified can be rationalized, assuming 13 glucosinolates in the seeds and 12 in the leaves. Among the volatile hydrolysis products observed, those derived from allylglucosinolates and 3‐methylsulphinylpropylglucosinolate (glucoiberin) were prominent. Copyright © 2003 John Wiley & Sons, Ltd.
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William C. K. Chiang, Donald Pusateri, Richard E. A. Leitz · Journal of Agricultural and Food Chemistry · 1998 · 105 citations
Food Analysis, Secondary Metabolites, Sulforaphane Nitrile +19
Mass Spectra of Isothiocyanates.
Anders Kjær, Mamoru Ohashi, J. M. WILSON et al. · Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry · 1963 · 104 citations · Full text