Results 201 to 210 of about 24,276 (243)
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Glucosinolates from Cardaria draba
Fitoterapia, 2002A new glucosinolate salt, L-prolinium 4-(methylsulfinyl)butyl glucosinolate, was isolated from the flowering heads of Cardaria draba and characterized by current spectroscopic methods.
Antoine, Fréchard +3 more
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Glucosinolate structures in evolution
Phytochemistry, 2012By 2000, around 106 natural glucosinolates (GSLs) were probably documented. In the past decade, 26 additional natural GSL structures have been elucidated and documented. Hence, the total number of documented GSLs from nature by 2011 can be estimated to around 132.
Agerbirk, Niels, Olsen, Carl Erik
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BIOLOGY AND BIOCHEMISTRY OF GLUCOSINOLATES
Annual Review of Plant Biology, 2006Glucosinolates are sulfur-rich, anionic natural products that upon hydrolysis by endogenous thioglucosidases called myrosinases produce several different products (e.g., isothiocyanates, thiocyanates, and nitriles). The hydrolysis products have many different biological activities, e.g., as defense compounds and attractants. For humans these compounds
Halkier, Barbara Ann +1 more
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Glucosinolates in Bretschneideraceae
Biochemical Systematics and Ecology, 19892-Hydroxy-2-methylpropyl- and 3,4-dihydroxybenzyl-glucosinolate have been identified as constituents of leaf material of Bretschneidera sinensis. The finding is discussed in the light of the rather tumultuous taxonomic history of this taxon.
D.E. Boufford +3 more
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Glucosinolate in Leindottersamen
Lipid / Fett, 1995AbstractDie Studie berichtet über Art und Menge der Glucosinolate (GLS) in Leindottersaaten. Im Vergleich zur Literatur wird gezeigt, daß neben dem Glucocamelinin (10‐Methylsulfinyldecyl‐GLS) zwei weitere Thioglucoside vorkommen. Durch GC/MS‐ und Thermospray/MS‐Untersuchungen wurden sie als 9‐Methylsufinylnonyl‐ bzw.
R. Lange +4 more
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Tetrahedron, 1980
Abstract A high yielding synthesis of 2-phenethylglucosinolate is described. The method should also be directly applicable to most (if not all) other glucosinolates.
V. Gil, A.J. MacLeod
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Abstract A high yielding synthesis of 2-phenethylglucosinolate is described. The method should also be directly applicable to most (if not all) other glucosinolates.
V. Gil, A.J. MacLeod
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