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  • 1
    ISSN: 0170-2041
    Keywords: 1,3-Dioxolanes ; 1,3-Oxazolidines ; α-Oxocarboxylic acids ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of Trialkylsilyl Trifluoromethanesulfonates XI.  -  Synthesis of α-Oxocarboxylic Acid Derivatives from 2-O-Functionalized Trimethylsilyl Ketene AcetalsThe cyclic ketene acetals 3, 5 are prepared from the dioxolanone 2 resp. the oxazolidinediones 4 by silylation with trimethylsilyl triflate (1)/triethylamine. In an aldol addition/Peterson olefination reaction catalysed by 1 the ketene acetals 3, 5 yield the (E/Z)-benzylidene derivatives 7, 12, 13 in reaction with aromatic aldehydes 6. In a side reaction the α-(trimethylsilyl)benzylidene derivatives 8 are formed from 3 and 6. Compounds 7 can be hydrolysed to yield α-ketocarboxylic acids 14. The latter are also obtained via β-elimination of trimethylsilanol from 2,3-bis(trimethylsiloxy)carboxylic acid esters 15 with trifluoroacetic acid anhydride/DMAP/pyridine.
    Additional Material: 11 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 12 (1973), S. 119-126 
    ISSN: 0570-0833
    Keywords: Heterocycles ; Intramolecular reactions ; Acylation ; Nitrile hydrogen halide adducts ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Five-membered, six-membered, and seven-membered aza-, diaza-, and thiazaheterocycles can be prepared by cyclization of. ω-cyano carboxylic acid halides in the presence of hydrogen halides in aprotic solvents. Nitrile-hydrogen halide adducts occur as intermediates in this novel heterocycle synthesis of wide application. The acylating cyclizations of nitriles in protonic media, which proceed via imidic esters or amides, are not discussed.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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