2019
DOI: 10.1016/j.jorganchem.2019.04.021
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Cross-coupling reactions catalysed by palladium pincer complexes. A review of recent advances

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Cited by 142 publications
(62 citation statements)
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“…Various reactions for forming a C–C bond are currently under study because of their significant applications . Among them, the Mizoroki–Heck reaction is, perhaps, the most strategic process for the arylation of olefins through palladium‐catalyzed C–C formation reactions . Although numerous attempts at designing a green, simple, cost‐effective, and efficient approach for this reaction have been made, there is still ample scope for improvement.…”
Section: Introductionmentioning
confidence: 99%
“…Various reactions for forming a C–C bond are currently under study because of their significant applications . Among them, the Mizoroki–Heck reaction is, perhaps, the most strategic process for the arylation of olefins through palladium‐catalyzed C–C formation reactions . Although numerous attempts at designing a green, simple, cost‐effective, and efficient approach for this reaction have been made, there is still ample scope for improvement.…”
Section: Introductionmentioning
confidence: 99%
“…After six successive cycles, the Cu-AIA-PC-Pd catalystr emains substantially active and no significant decreasesi nt he catalytic efficiency are observed ( Figure S22). Compared with the catalysts reported in literatures (TableS5), [73][74][75][76][77][78][79][80][81][82][83] the obtained Cu-AIA-PC-Pd also exhibits excellentc atalytic activity.T he results confirm that Cu-AIA as a2 Dcarriertos upport metal catalysts is feasible.…”
Section: Catalytic Performanceand Reaction Mechanism Analysismentioning
confidence: 64%
“…During the past three decades, pincer palladium catalysts have been developed and used for cross‐coupling reactions. [ 22,45 ] Hence, the catalytic activities of complexes 2a–c were evaluated in Suzuki–Miyaura couplings (Scheme 8). [ 34,40 ] For this purpose, the reactions were performed using phenyl bromide, phenylboronic acid, 0.1 mol‐% of catalyst, K 2 CO 3 , toluene at 100 °C for 90 min.…”
Section: Poczp‐aryl Pincer Metal Complexesmentioning
confidence: 99%