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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 1088-1094 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the C-Acylation with DiacylaminesThe acylation of methyl ketones (1a-c) with N-methyldiacetamide, N-substituted monocyclic imides (2a-d), N-acyl lactams (4a-e) as well as a bicyclic imide (7) in the presence of sodium hydride to give 3a-f, 5a-e, 6a-c, and 8 is described.
    Notes: Die Acylierung von Methylketonen (1a-c) mit N-Methyl-diacetamid, N-substituierten monocyclischen Imiden (2a-d), N-Acyl-lactamen (4a-e) sowie einem bicyclischen Imid (7) in Gegenwart von Natriumhydrid zu 3a-f, 5a-e, 6a-c, und 8 wird beschrieben.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 114 (1981), S. 1836-1844 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Applications of Phase Transfer Catalysis, VIII1) Synthesis and some Reactions of Tetrasubstituted 6,6-Dihalogenobicyclo[3.1.0]hex-3-en-2-onesThe reaction of tetrasubstituted cyclopentadienones 1 with dichlorocarbene or dibromocarbene gives specifically the 6,6-dihalogenobicyclo[3.1.0]hex-3-en-2-ones 2 and 3. Reductive ring opening of 2 or 3 with LiAlH4 cleanly yields the tetrasubstituted 3-halogenophenols 4 and 5. Reaction of 2 or 3 with methylmagnesium iodide leads to 2,4-cyclohexadien-1-ones 13 and to 1-halogeno-5-methylene-1,3-cyclohexadienes 14.
    Notes: Die Reaktion der tetrasubstituierten Cyclopentadienone 1 mit Dichlorcarben bzw. Dibromcarben führt spezifisch zu den 6,6-Dihalogenbicyclo[3.1.0]hex-3-en-2-onen 2 bzw. 3, deren reduktive Ringöffnung mit LiAlH4 einen einfachen Weg zu den tetrasubstituierten 3-Halogenphenolen 4 bzw. 5 darstellt. Umsetzung von 2 bzw. 3 mit Methylmagnesiumiodid ermöglicht einen neuen Zugang zu 2,4-Cyclohexadien-1-onen 13 und zu 1-Halogen-5-methylen-1,3-cyclohexadienen 14.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 2402-2412 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Applications of Phase Transfer Catalysis, II. Synthesis of 2-Dihalogenomethyl-1,3-dioxolanes and 2-Dihalogenomethyl-1,3-dioxanes2-Substituted 1,3-dioxolanes 1a-35a react with dichlorocarbene generated by phase transfer catalysis via selective C(2)-H-insertion giving the 2-dichloromethyl-1,3-dioxolanes 1b-24b. and 26b-35b. In the same way the 2-dichloromethyl-1,3-dioxanes le, 2e, 4e-6e,12e, 26e, and 30e and the 2-dibromomethyl-1,3-dioxolanes 1c, 2c, 4c-6c, 12c, 26c, 28c, and 30c are prepared.
    Notes: 2-Substituierte 1,3-Dioxolane 1a-35a reagieren mit durch Phasentransfer-Katalyse erzeugtem Dichlorcarben unter selektiver C(2)-H-Insertion zu den 2-Dichlormethyl-1,3-dioxolanen 1b-24b und 26b-35b. Ebenso entstehen die 2-Dichlormethyl-1,3-dioxane 1e, 2e, 4e-6e, 12e, 26e und 30e und die 2-Dibrommethyl-1,3-dioxolane lc, 2c, 4c-6c, 12c, 26c, 28c und 30c.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 65 (1932), S. 413-418 
    ISSN: 0365-9631
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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