Szuroczki, Péter and Sámson, Judit and Kollár, László (2019) Synthesis of 5-Carboxamidotriazoles via Azide-Alkyne Cycloaddition–Aminocarbonylation Sequence. ChemistrySelect, 4 (19). pp. 5527-5530. ISSN 2365-6549
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Official URL: http://doi.org/10.1002/slct.201900848
Abstract
5-Carboxamidotriazoles were prepared in the palladium-catalyzed aminocarbonylation of the corresponding iodotriazole using various amines as N-nucleophiles under mild reaction conditions. The iodoheteroarene substrates were obtained in good yields in copper-catalysed azide-alkyne cycloaddition of iodoalkynes (2’-iodophenylacetylene and ethyl iodopropiolate) and benzyl azide.
Item Type: | Article |
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Subjects: | Q Science / természettudomány > QD Chemistry / kémia > QD04 Organic chemistry / szerves kémia |
Depositing User: | Pap Viktória |
Date Deposited: | 22 Nov 2019 12:11 |
Last Modified: | 22 Nov 2019 12:11 |
URI: | http://real.mtak.hu/id/eprint/103584 |
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