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Superelectrophilic chemistry of amino-nitriles and related substrates.


ABSTRACT: The superacid-promoted Houben-Hoesch reactions of amino-nitriles and related compounds have been studied. The nitriles form dicationic electrophiles and react with benzene in fair to good yields (12-95%). The intermediate iminium ions may also be reduced to the benzylic amines by NaBH(4) or H(2).

SUBMITTER: Raja EK 

PROVIDER: S-EPMC3110710 | biostudies-literature | 2011 Jun

REPOSITORIES: biostudies-literature

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Superelectrophilic chemistry of amino-nitriles and related substrates.

Raja Erum K EK   Klumpp Douglas A DA  

Tetrahedron 20110601 25


The superacid-promoted Houben-Hoesch reactions of amino-nitriles and related compounds have been studied. The nitriles form dicationic electrophiles and react with benzene in fair to good yields (12-95%). The intermediate iminium ions may also be reduced to the benzylic amines by NaBH(4) or H(2). ...[more]

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