Nagymihály, Zoltán and Kollár, László (2015) High-yielding synthesis of deepened cavitands bearing picolyl moieties on the upper rim. TETRAHEDRON, 71. pp. 2555-2560. ISSN 0040-4020
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Abstract
Conventional high-yielding reactions (such as etherification, condensation reactions) and palladium catalysed aminocarbonylation served as highly efficient synthetic tools for the synthesis of novel cav itands bearing Schiff-base and carboxamide/2-ketocarboxamide functionalities, respectively. In this way, two families of deepened cavitands with related structures possessing 2-, 3- and 4-picolylamine moieties on the upper rim have been synthesised. Unexpectedly high chemoselectivities towards tetracarbox amides and tetrakis(2-ketocarboxamides) have been observed. The aminocarbonylation of tetraiodoca vitand as an iodoaromatic substrate proved to be highly selective in two aspects: (i) no substantial formation of either the mono-, di- or trifunctionalized products was observed and (ii) no ‘mixed’ products possessing both carboxamide and 2-ketocarboxamide fragments, due to selective simple and double carbon monoxide insertion, were detected.
Item Type: | Article |
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Subjects: | Q Science / természettudomány > QD Chemistry / kémia |
Depositing User: | Pap Viktória |
Date Deposited: | 12 Feb 2016 11:54 |
Last Modified: | 12 Feb 2016 11:54 |
URI: | http://real.mtak.hu/id/eprint/33355 |
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