1973
DOI: 10.1002/chin.197346295
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ChemInform Abstract: SILYLIERUNG VON NITROVERBINDUNGEN 4. MITT. TRIMETHYLSILYLIERUNG DES NITROESSIGSAEUREMETHYLESTERS UND DES DINITROMETHANS

Abstract: Der Ester (I) und Dinitromethan (II) werden mit dem Hanrstoff (III) zu den Trimethylsilylestern von Nitronsäuren (IV), (V) umgesetzt.

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“…46,56,58,61,65,[71][72][73]79 In 1972 Ioffe and co-workers80 suggested using the silyl esters of nitronic acids as a 1,3-dipolar component, which unlike their alkyl analogues is stable and retains the ability of cycloaddition to olefins. [81][82][83][84][85][86][87][88][89][90][91][92] The intramolecular reactions of the nitronate group with double bonds are known too. For instance, the interaction of tetranitromethane with one of the double bonds of hexa-1,5-diene gives a nitronic ester which is then added to the other double bond forming bicyclic compound 2 (Scheme l).…”
Section: Synthesismentioning
confidence: 99%
“…46,56,58,61,65,[71][72][73]79 In 1972 Ioffe and co-workers80 suggested using the silyl esters of nitronic acids as a 1,3-dipolar component, which unlike their alkyl analogues is stable and retains the ability of cycloaddition to olefins. [81][82][83][84][85][86][87][88][89][90][91][92] The intramolecular reactions of the nitronate group with double bonds are known too. For instance, the interaction of tetranitromethane with one of the double bonds of hexa-1,5-diene gives a nitronic ester which is then added to the other double bond forming bicyclic compound 2 (Scheme l).…”
Section: Synthesismentioning
confidence: 99%