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 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | |
Online-Zugang: | Volltext |
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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%). |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c8cc03447h |