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Most Requested Journal Articles 4Q06-Chemistry and Related
Following is one of the journal articles most requested by researchers using CAS electronic products.
CAPLUS COPYRIGHT 2007 ACS on STN
CuI-catalyzed coupling reaction of electron-deficient aryl iodides with aliph. primary amines occurred under the promotion of N-methylglycine. Using L-proline as the promoter, coupling reaction of aryl iodides or aryl bromides with aliph. primary amines, aliph. cyclic secondary amines, or electron-rich primary arylamines proceeded. Also, an intramol. coupling reaction between aryl chloride and primary amine moieties gave indoline. Coupling reaction of aryl iodides with indole, pyrrole, carbazole, imidazole, or pyrazole was also carried out. And, finally, coupling of electron-deficient aryl bromides with imidazole or pyrazole occurred. The corresponding N-aryl products were obtained in good to excellent yields. N,N-dimethylglycine promoted the coupling reaction of electron-rich aryl bromides with imidazole or pyrazole to afford the corresponding N-aryl imidazoles. The possible action of amino acids in these coupling reactions is discussed. Updated 4/24/2007 11:14:22 AM
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