Pregled bibliografske jedinice broj: 368685
Transformation of indole-3-ethanol to new conjugates in plants
Transformation of indole-3-ethanol to new conjugates in plants // Conjugated plant hormones. Structure, metabolism and function. Proceedings of the international symposium. / Schreiber, Klaus ; Schütte, H. R. ; Sembdner, Günther (ur.).
Berlin: VEB Deutscher Verlag der Wissenschaften, 1987. str. 69-74 (predavanje, međunarodna recenzija, cjeloviti rad (in extenso), znanstveni)
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Naslov
Transformation of indole-3-ethanol to new conjugates in plants
Autori
Laćan, Goran ; Lewer, Paul ; Magnus, Volker ; Iskrić, Sonja
Vrsta, podvrsta i kategorija rada
Radovi u zbornicima skupova, cjeloviti rad (in extenso), znanstveni
Izvornik
Conjugated plant hormones. Structure, metabolism and function. Proceedings of the international symposium.
/ Schreiber, Klaus ; Schütte, H. R. ; Sembdner, Günther - Berlin : VEB Deutscher Verlag der Wissenschaften, 1987, 69-74
Skup
Conjugated plant hormones. Structure, metabolism and function
Mjesto i datum
Gera, Njemačka, 03.11.1986. - 07.11.1986
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Craterellus cornucopioides; basidiomycete; indole-3-ethanol; tryptophol; indole-3-ethyl oleate; indole-3-ethyl dehydrocrepenynate
Sažetak
On feeding with indole-3-ethanol (tryptophol), many plants and microorganisms convert the alcohol to non-polar esters. Particularly large amounts of these conjugates were formed by the basidiomycete Craterellus cornucopioides (L.) ex Pers. which was, thus, chosen to supply the quantities necessary for structural studies. Chromatographic purification afforded two esters, for which C-13 NMR spectra suggested the structures, indole-3-ethyl oleate and indole-3-ethyl dehydrocrepenynate. Authentic standards were synthesized and showed identical C-13 NMR spectra.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb