Highly enantioselective Friedel-Crafts alkylation of ,-dialkylanilines with -β-nitrostyrene catalyzed by a homochiral metal-organic framework

The first enantioselective Friedel-Crafts alkylation of N , N -dialkylanilines with trans -β-nitrostyrene catalyzed by a homochiral metal-organic framework constructed from ( R )-2,2′-dihydroxy-1,1′-binaphthyl-6,6′-dicarboxylic acid has been developed. The reaction proceeded in high yields (∼96%) wi...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2018-06, Vol.54 (49), p.6328-6331
Hauptverfasser: Tanaka, Koichi, Sakuragi, Kenji, Ozaki, Hiroto, Takada, Yoshiki
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Zusammenfassung:The first enantioselective Friedel-Crafts alkylation of N , N -dialkylanilines with trans -β-nitrostyrene catalyzed by a homochiral metal-organic framework constructed from ( R )-2,2′-dihydroxy-1,1′-binaphthyl-6,6′-dicarboxylic acid has been developed. The reaction proceeded in high yields (∼96%) with excellent enantioselectivities (∼98% ee). The first enantioselective Friedel-Crafts alkylation of N , N -dialkylanilines with trans -β-nitrostyrene catalyzed by a homochiral MOF afforded the addition products in high yields (∼96%) with excellent ee (∼98%).
ISSN:1359-7345
1364-548X
DOI:10.1039/c8cc03447h