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  • Articles: DFG German National Licenses  (2)
  • 1985-1989  (2)
  • Inorganic Chemistry  (2)
  • 1,3-Dithietane 1,1,3,3-tetraoxide
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  • Articles: DFG German National Licenses  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 121 (1988), S. 689-699 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Cycloaddition Reactions of Heterocumulenes, XXIX.  -  Reactions of Thioketenes with IsocyanatesThe [2 + 2] cycloaddition of thioketenes 1a-f to isocyanates 2a-f yields 4-thioxo-2-azetidinones 3 as main products, which may isomerize to 4-imino-2-thietanones 5. In competing reactions, 2,4-azetidinediones 8, N-sulfonylamides 9, and 3H-1,2,4-dithiazoles 15 are formed. Thioketenes 1 react with chlorosulfonyl isocyanate (20b) to give N-unsubstituted 4-thioxo-2-azetidinones 22. Depending on the thioketene 1 and the reaction conditions, compounds 23-26 also result. The constitutions of 15b and 23a were determined by X-ray structural analyses.
    Notes: Die [2 + 2]-Cycloaddition der Thioketene 1a-f an die Isocyanate 2a-f liefert als Hauptprodukt 4-Thioxo-azetidinone 3, die sich zu 4-Imino-2-thietanonen 5 isomerisieren können. In Konkurrenzreaktionen werden 2,4-Azetidindione 8, N-Sulfonylamide 9 und 3H-1,2,4-Dithiazole 15 gebildet. Mit Chlorsulfonylisocyanat (20b) reagieren die Thioketene 1 zu N-unsubstituierten 4-Thioxo-2-azetidinonen 22. Je nach Thioketen 1 und Reaktionsführung resultieren auch die Verbindungen 23-26. Die Konstitution von 15b und 23a wurde durch Röntgenstrukturanalyse bestimmt.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 121 (1988), S. 1165-1175 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Thioketene Syntheses, VIII.  -  Thioketenes by [3+2] Cycloreversion of 1,3-Dithiolane Derivatives2-Alkylidene-1,3-dithiolanes are transformed into S,S-dioxides 1 and S-ethyl- 2 or S-arylsulfonium salts 3. After deprotonation at C-5 they form in a [3 + 2] cycloreversion thioketenes 5, which can be trapped as thioamides 17, 18. The stabilized thioketenes 5e, i-k afford 1:1 cycloadducts 24a, b, 27a-d with azomethines; in addition, thioketene 5j provides a dimer 28j, which was characterized by an X-ray structural investigation.
    Notes: 2-Alkyliden-1,3-dithiolane werden in S,S-Dioxide 1 und S-Ethyl-2 oder S-Arylsulfonium-Salze 3 übergeführt. Nach Deprotonierung an C-5 bilden sich in einer [3 + 2]-Cycloreversion Thioketene 5, die als Thioamide 17, 18 abgefangen werden können. Die stabilisierten Thioketene 5e,i-k liefern mit Azomethinen 1: 1-Cycloaddukte 24a,b, 27a-d; das Thioketen 5j reagiert daneben zu einem Dimeren 28j, das durch Röntgenstrukturanalyse charakterisiert wurde.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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