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Iodination of Phenylacetylene and Some Transformations of the Resulting Iodo Derivatives
An efficient procedure has been proposed for the reaction of molecular iodine with phenylacetylene in the presence of cadmium(II) acetate in DMSO at room temperature, and the reactant ratio has been optimized for the iodination process. Mercuration–demercuration of iodoethynylbenzene with molecular...
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Published in: | Russian journal of organic chemistry 2024-09, Vol.60 (9), p.1698-1704 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | An efficient procedure has been proposed for the reaction of molecular iodine with phenylacetylene in the presence of cadmium(II) acetate in DMSO at room temperature, and the reactant ratio has been optimized for the iodination process. Mercuration–demercuration of iodoethynylbenzene with molecular iodine and oxidative homocoupling in the presence of dilithium tetrachlorocuprate have been performed. |
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ISSN: | 1070-4280 1608-3393 |
DOI: | 10.1134/S1070428024090124 |