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- W4230625057 abstract "Eine gemeinsame Route führte zu einer kurzen Synthese der Sesquiterpenoide Merrilacton A und Anislacton A. Eine reduktive Epoxid-Spaltung mit TiIII und eine radikalische Cyclisierung wurden genutzt, um das quartäre C9-Zentrum im Kern des BC-Bicyclus einzurichten. Selektive Lactonisierungssequenzen legen dann regiodivergente Pfade zum Merrilacton A (formale Synthese) und zum Anislacton A (Totalsynthese) fest." @default.
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- W4230625057 date "2010-10-21" @default.
- W4230625057 modified "2023-09-29" @default.
- W4230625057 title "Synthesis of (±)-Merrilactone A and (±)-Anislactone A" @default.
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- W4230625057 doi "https://doi.org/10.1002/ange.201005156" @default.
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