Pd-Catalyzed intermolecular C-H bond arylation reactions: effect of bulkiness of carboxylate ligands
A bulky carboxylic acid bearing one 1-adamantylmethyl and two methyl substituents at the α-position is demonstrated to work as an efficient carboxylate ligand source in Pd-catalyzed intermolecular C(sp 2 )-H bond arylation reactions. The reactions proceeded smoothly under mild conditions, taking adv...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2020-04, Vol.56 (27), p.3843-3846 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A bulky carboxylic acid bearing one 1-adamantylmethyl and two methyl substituents at the α-position is demonstrated to work as an efficient carboxylate ligand source in Pd-catalyzed intermolecular C(sp
2
)-H bond arylation reactions. The reactions proceeded smoothly under mild conditions, taking advantage of the steric bulk of the carboxylate ligands.
A bulky carboxylic acid bearing one 1-adamantylmethyl and two methyl substituents at the α-position is demonstrated to work as an efficient carboxylate ligand source in Pd-catalyzed intermolecular C(sp
2
)-H bond arylation reactions. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/d0cc01129k |