Synthese und Reaktivität von γ-Triphenylstannyl-α-aminobuttersäure-derivaten / Synthesis and Reactivity of γ-Triphenylstannyl-α-aminobutyric Acid Derivatives

Autor: Dölling, Karin, Krug, André, Hartung, Helmut, Weichmann, Horst
Zdroj: Zeitschrift für Naturforschung B; January 1997, Vol. 52 Issue: 1 p9-16, 8p
Abstrakt: Ph3SnCH2CH2CH(NHCOOCH2Ph)COOCH3(1) is synthesized by hydrostannation of methyl N-(benzyloxycarbonyl)vinylglycinate with Ph3SnH. The reaction of 1 with HCl in CH3OH and with bromine in CHCl13yields the halostannylsubstituted compounds Ph3-nXnSnCH2CH2CH(NHCOOCH2Ph)COOCH3(2 - 4) (n = 1, 2; X = Cl, Br). By saponification with one equivalent of NaOH and subsequent acidification with HCl 1 is transformed into the free acid Ph3SnCH2CH2CH(NHCOOCH2Ph)COOH (5) that undergoes cyclization into the 1,2-oxastanninane 6 with intramolecular elimination of benzene. IR, NMR data and the determination of the crystal structure of Ph2BrSnCH2CH2CH(NHCOOCH2Ph)COOCH3(3) reveal for 2 and 3 an intramolecular coordination of the NC(O)O-group at the tin atom to form a seven-membered ring
Databáze: Supplemental Index