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- W2126909725 abstract "Konvergenter geht's nicht: Dank einer ausgeklügelten Schutzgruppenstrategie gelingt das „Endspiel”︁ der Totalsynthese von Calicheamicin γ , aus dem Aglycon ent ‐ 1 (siehe vorherigen Beitrag; R = SSMe, ketalgeschützt) und dem Glycosyl‐Donor 2 in nur drei Schritten: Kupplung, Deketalisierung und Abspaltung der Schutzgruppen. magnified image" @default.
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- W2126909725 date "1994-04-18" @default.
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- W2126909725 title "Eine konvergente Totalsynthese von Calicheamicin γI1" @default.
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- W2126909725 doi "https://doi.org/10.1002/ange.19941060823" @default.
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