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Aminothiazoles and aminothiadiazoles as nucleophiles in aminocarbonylation of iodobenzene derivatives

Gergely, Máté and Kollár, László (2018) Aminothiazoles and aminothiadiazoles as nucleophiles in aminocarbonylation of iodobenzene derivatives. TETRAHEDRON, 74. pp. 2030-2040. ISSN 0040-4020

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Abstract

Various 2-, 3- and 4-substituted iodobenzenes were aminocarbonylated using aminothiazole and aminothiadiazole derivatives in palladium-catalysed reaction. The reaction is chemospecific toward the corresponding carboxamides. Consequently, the application of the above N-nucleophiles provided the N- 1,3-thiazol-2-yl- and N-1,3,4-thiadiazol-2-ylcarboxamides in moderate to high yields. Due to the facile work-up of the reaction mixture isolated yields of 90% or higher were obtained in most cases.

Item Type: Article
Uncontrolled Keywords: Palladium, Iodoarene, Thiazole, Carbonylation, Carbon monoxide, Carboxamide
Subjects: Q Science / természettudomány > QD Chemistry / kémia
Depositing User: Pap Viktória
Date Deposited: 21 Jan 2019 13:26
Last Modified: 21 Jan 2019 13:26
URI: http://real.mtak.hu/id/eprint/90201

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