The action mechanism of ethylenediamine, tetramethylethylenediamine, and disodium ethylenediaminetetraacetic acid (EDTA-2Na) as corrosion inhibitors for aluminum radiators has been clarified, and the scientific laws between functional groups and ...
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Organocatalytic Regio‐ and Enantioselective Friedel‐Crafts Alkylation of N‐Aryl Anilines with Aurone‐Derived Azadienes: Access to Benzofuran Embedded Triarylmethanes
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A catalytic asymmetric Friedel-Crafts alkylation of N-aryl anilines with aurone-derived azadienes for the first synthesis of benzofuran and N-aryl aniline containing triarylmethanes has been developed.
Abstract
Herein, we disclose a catalytic asymmetric Friedel-Crafts alkylation of N-aryl anilines with aurone-derived azadienes for the first synthesis of benzofuran and N-aryl aniline containing triarylmethanes. An easily available chiral phosphoric acid, TRIP, was found to be effective for this reaction. The triarylmethanes with benzofuran and N-aryl aniline motifs were obtained in moderate yields with high regio- and good to high enantioselectivities. The scope of the reaction was broad and few synthetic transformations have been demonstrated.
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