2014
DOI: 10.1016/j.inoche.2014.03.002
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Palladium(II) thiosemicarbazone complex: Synthesis, structure and application to carbon–oxygen cross-coupling reaction

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Cited by 19 publications
(4 citation statements)
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“…Published results of the use of thiosemicarbazone complexes as described above for Cheteroatom coupling reactions are summarised in Table 4. Apart from the above C-N coupling reactions, there has also been one report by Suganthy et al of C-O coupling catalysed by a thiosemicarbazone complex [146]. Thus the coupling of p-cresol with a number of aryl halides containing electron-withdrawing or electron-donating groups could be effected, with moderate to very good yields, in DMF at 80 • C after 12 h in an inert atmosphere using a 1 mol% loading of the catalyst [PdCl(PPh 3 )L] (42), where L is the bidentate N,S-chelating ligand derived from the deprotonation of 3-methyl-thiophene-2-carboxaldehyde thiosemicarbazone (Figure 7).…”
Section: Carbon-heteroatom Coupling Reactionsmentioning
confidence: 99%
“…Published results of the use of thiosemicarbazone complexes as described above for Cheteroatom coupling reactions are summarised in Table 4. Apart from the above C-N coupling reactions, there has also been one report by Suganthy et al of C-O coupling catalysed by a thiosemicarbazone complex [146]. Thus the coupling of p-cresol with a number of aryl halides containing electron-withdrawing or electron-donating groups could be effected, with moderate to very good yields, in DMF at 80 • C after 12 h in an inert atmosphere using a 1 mol% loading of the catalyst [PdCl(PPh 3 )L] (42), where L is the bidentate N,S-chelating ligand derived from the deprotonation of 3-methyl-thiophene-2-carboxaldehyde thiosemicarbazone (Figure 7).…”
Section: Carbon-heteroatom Coupling Reactionsmentioning
confidence: 99%
“…Published results of the use of thiosemicarbazone complexes as described above for Cheteroatom coupling reactions are summarised in Table 4. Apart from the above C-N coupling reactions, there has also been one report by Suganthy et al of C-O coupling catalysed by a thiosemicarbazone complex [146]. Thus the coupling of p-cresol with a number of aryl halides containing electron-withdrawing or electron-donating groups could be effected, with moderate to very good yields, in DMF at 80 • C after 12 h in an inert atmosphere using a 1 mol% loading of the catalyst [PdCl(PPh 3 )L] (42), where L is the bidentate N,S-chelating ligand derived from the deprotonation of 3-methyl-thiophene-2-carboxaldehyde thiosemicarbazone (Figure 7).…”
Section: Carbon-heteroatom Coupling Reactionsmentioning
confidence: 99%
“…These have aroused great interest due to their wide range of applications. Their biological activity depends on the parent aldehyde or ketone [1][2][3]; also, palladium (II) complexes have proved to be useful as catalysts in cross coupling reactions like the Heck and Suzuki-Miyaura cross-coupling reaction [4][5][6][7].…”
Section: Introductionmentioning
confidence: 99%