Abstract
Neodictyoprolenol [(-)-(3S)-(1,5Z,8Z)-undecatrien-3-ol] and dictyoprolenol [(-)-(3S)-(1,5Z,8Z)-undecadien-3-ol]), which had been proposed as possible biosynthetic intermediates of the sex pheromones of marine brown algae such as dictyopterene B [(-)-trans-1((1′E,3′Z)-hexadienyl)-2-vinylcyclopropane]. D′ [(+)-6-((1′Z)-butenyl)-1,4-cycloheptadiene] and C′ [(+)-6-butyl-1,4-cycloheptadiene], were again identified in the essential oils from Dictyopteris prolifera, D. latiscula, and in D. undulata, together with the C11-related volatile compounds such as neodictyoprolene, dictyoprolene and dictyopterenes. Incubation of D. prolifela preparation with racemic neodictyoprolenol and dictyoprolenol as substrates showed (S)-enantioselective decreases of the added substrates and increases in dictyopterenes. From these results, a possible pathway to form dictyopterenes is discussed.
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Yamamoto, Y., Akakabe, Y., Matsui, K., Shimizu, H., & Kajiwara, T. (2001). Neodictyoprolenol and dictyoprolenol, the possible biosynthetic intermediates of dictyopterenes, in the Japanese brown algae Dictyopteris. Zeitschrift Fur Naturforschung - Section C Journal of Biosciences, 56(1–2), 6–12. https://doi.org/10.1515/znc-2001-1-202
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