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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 21 (1982), S. 36-49 
    ISSN: 0570-0833
    Keywords: Acyl cyanides ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Through improved and novel syntheses, acyl cyanides - especially aliphatic acyl cyanides - have become so readily accessible that numerous synthetic applications present themselves. The present review surveys the development of the chemistry of the acyl cyanides during the last 25 years. The syntheses and most important reaction possibilities of R—CO—CN are outlined in four large schemes: reactions of the CO- and CN-groups - in each case with preservation of the carbon skeletal framework - as well as acylations with cleavage of cyanide ions.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0570-0833
    Keywords: Heavy main-group elements ; Main group elements ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aside from elements of the 2nd row, and one element of the 3rd row of the periodic system - Si, P, S, and Se, respectively, whose organoelement groups such as Me3Si and Ph3P⊕ have proven useful in numerous organic syntheses - other elements of the 3rd as well as 4th and 5th row (Ge, As, Sn, Sb, Te, Pb, Bi) can also be used as components of synthetically useful organoelement groups, the elements As, Sn, and Pb, in particular, offering certain advntages over the others. Some of these organoelement groups are suitable equivalents for Li- or halogen-substituents attached to carbon; they stabilize carbanionic centers (minimum of this effect at the 3rd-row elements), and owing to their suitability as leaving groups in β-eliminations, also open up interesting synthetic possibilities. The thermally unduced syn- and silica-gel induced anti-elimination of Ph3Sn, Ph2Sb, Ph3Pb, together with β-OH, are novel. With the newly synthesized compounds PhnEl - Ch2 - Li (El = Sn, Pb, As, Sb, Bi) and other α- and β-lithiated RnEl- and Ph2As(O)-reagents such organoelement groups can be introduced into organic compounds and exploited in organic and organoelement synthesis.
    Additional Material: 13 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 21 (1982), S. 96-108 
    ISSN: 0570-0833
    Keywords: Lewis acids ; Alkylation ; Carbonyl compounds ; Synthetic methods ; Silyl enol ethers ; C-C coupling ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Carbonyl compounds undergo α-alkylation via the corresponding silyl enol ethers using SN1 active alkyl halides or acetates in the presence of Lewis acids. This methodology extends the scope of carbonyl chemistry considerably, since SN1 active alkylating agents are generally base sensitive and therefore unsuitable for reactions with enolate anions or nitrogen analogs. A prime example is the α-tert-alkylation of aldehydes, ketones and esters.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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