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- W2085148665 abstract "Die nucleophile Substitution der OTf‐Gruppen in 1 a,b durch Amine und Aminoalkohole ermöglicht einen neuen Zugang zu N 2 ‐alkylierten Desoxyguanosinen . Ausgehend von 1 a, b werden biologisch relevante N 2 ‐Desoxyguanosin‐Addukte von cancerogenen Alkylantien, z.B. das des ultimal cancerogenen (±)‐ anti ‐Dihydrodiolepoxids von Benzo[ a ]pyren, erhalten. TBDMS = tert ‐Butyldimethylsilyl. a : R 1 = p ‐Nitrophenylethyl, b R 1 = Allyl; Tf = CF 3 SO 2 . magnified image" @default.
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- W2085148665 date "1993-03-01" @default.
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- W2085148665 title "Die Aktivierung der C-2-Position von Purin durch die Trifluormethansulfonatgruppe: Synthese von N2-alkylierten Desoxyguanosinen" @default.
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- W2085148665 doi "https://doi.org/10.1002/ange.19931050310" @default.
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