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Catalytic enantioselective electrophilic aromatic reactions

Despite the prevalence and importance of atropisomerism in organic structures, the field of asymmetric catalysis has not yet recorded extensive success in the development of catalysts, which control this stereochemical feature. Indeed, catalytic reactions of this nature are presently rare and only modest atropi-somer selectivity has been observed. In this context. Miller s group recently developed the DKR of biaryl atropisomers via peptide-catalysed asymmetric bromination. The reaction proceeded via an atropisomer-selective electrophilic aromatic substitution reaction using a simple bromination reagent such as A7-bromophthtalimide. As shown in Scheme 5.27, a series of chiral bromi-nated biaryl compounds could be prepared with excellent enantioselectivities of... [Pg.259]


See other pages where Catalytic enantioselective electrophilic aromatic reactions is mentioned: [Pg.150]    [Pg.287]    [Pg.193]    [Pg.84]    [Pg.48]    [Pg.1190]    [Pg.229]    [Pg.387]    [Pg.33]    [Pg.341]    [Pg.744]    [Pg.744]   


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Catalytic reactions aromatization

Electrophile reactions Electrophilic aromatic

Electrophiles enantioselectivity

Electrophilic aromatic reactions

Enantioselective reaction

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