Preliminary results of an original approach to 4-substituted-2-phenylimidazoles starting from readily available N-propargyl-benzamidine and aryl halides are reported. Best yields were obtained using aryl halides bearing an electron-withdrawing group. Plausible mechanisms are also discussed.

Palladium catalyzed synthesis of 4-substituted-2-phenylimidazoles from N-propargyl-benzamidine / G. Abbiati, A. Arcadi, V. Canevari, E. Rossi. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 48:48(2007), pp. 8491-8495. [10.1016/j.tetlet.2007.09.153]

Palladium catalyzed synthesis of 4-substituted-2-phenylimidazoles from N-propargyl-benzamidine

G. Abbiati
Primo
;
V. Canevari
Penultimo
;
E. Rossi
Ultimo
2007

Abstract

Preliminary results of an original approach to 4-substituted-2-phenylimidazoles starting from readily available N-propargyl-benzamidine and aryl halides are reported. Best yields were obtained using aryl halides bearing an electron-withdrawing group. Plausible mechanisms are also discussed.
imidazole; amidine; alkynes; homogeneous catalysis; palladium; Domino reaction; aminopalladation
Settore CHIM/06 - Chimica Organica
2007
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/39594
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