Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Articles: DFG German National Licenses  (1)
  • 1,2-oxastannolane  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 63-71 
    ISSN: 0044-2313
    Keywords: diethyl triorganostannylmethyl N-acyl aminomalonates ; ethyl 3-(trimethylstannyl)-N-acyl alaninates ; 1,2-oxastannolane ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: C-Stannylmethylated N-Acetyl- and N-Formyl-aminomalonic Acid DerivativesTin compounds of the type Me3SnCH2C(NHCOR) · (COOEt)2 (1: R = CH3; 2: R = H) are synthesized by reaction of acylaminomalonates with iodomethyl trimethylstannane. The halogenation of 1 and 2 yields the halostannylsubstituted compounds Me3-nXnSnCH2C(NHCOR)(COOEt)2 3-6 (R = Me, H; n = 1, 2; X = Cl, Br). The decarbethoxylation (KRAPCHO reaction) of 1 and 2 gives ethyl 3-(trimethylstannyl)-N-acyl alaninates (7 and 8). With one equivalent KOH 1 and 2 are transformed into the monoethyl malonates of the type Me3SnCH2C(NHCOR)(COOH)(COOEt) (9: R = CH3), which convert simultaneously under decarboxylation into 7 and 8 and by cyclisation under elimination of methane into the 1,2-oxastannolane derivatives 10 and 11. IR, NMR data and the determination of the crystal structure reveal for MeBr2SnCH2C(NHCOCH3)(COOEt)2 (5) hexacoordinated tin by intramolecular coordination of the amide-CO and one of the ester-CO groups.
    Notes: Zinnverbindungen des Typs Me3SnCH2C(NHCOR)(COOEt)2 (1: R = CH3; 2: R = H) werden durch Umsetzung von Acylaminomalonsäureestern mit Iodomethyltrimethylstannan dargestellt. Die Halogenierung von 1 und 2 liefert die halogenostannylsubstituierten Verbindungen Me3-nXnSnCH2C(NHCOR)(COOEt)2 3-6 (R = Me, H; n = 1, 2; X = Cl, Br). Die Decarbethoxylierung (KRAPCHO-Reaktion) von 1 und 2 führt zu 3-(Trimethylstannyl)-N-acyl-alaninethylestern (7 und 8). Mit einem Äquivalent KOH werden 1 und 2 in die Monoethylester des Typs Me3SnCH2C(NHCOR)(COOH)(COOEt) (9: R = CH3) überführt, die sich in Folgereaktionen sowohl unter Decarboxylierung zu 7 bzw. 8 als auch durch Cyclisierung unter Methanabspaltung zu den 1,2-Oxastannolanderivaten 10 bzw. 11 umwandeln. IR-, NMR-Daten und die Bestimmung der Kristallstruktur beweisen für MeBr2SnCH2C(NHCOCH3)(COOEt)2 (5) hexakoordiniertes Zinn durch intramolekulare Koordination der Amid-CO- sowie einer Ester-CO-Gruppe.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...