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- W2145503822 abstract "Licht in die enantioselektive Synthese bringt das Produkt 1, bei dessen Bildung erstmalig eine templatgesteuerte [2+2]-Photocycloaddition für eine Naturstoffsynthese genutzt wurde. Eine Retro-Benzilsäure-Umlagerung (zu 2), eine Claisen-Umlagerung (zu 3) und eine Ringschlussmetathese spielen weitere entscheidende Rollen in der Synthese des Alkaloids (+)-Meloscin (4)." @default.
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- W2145503822 date "2008-06-23" @default.
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- W2145503822 title "Enantioselektive Totalsynthese des<i>Melodinus</i>-Alkaloids (+)-Meloscin" @default.
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- W2145503822 doi "https://doi.org/10.1002/ange.200800693" @default.
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