2003
DOI: 10.1016/s0040-4039(03)01686-1
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Improved Sonogashira CC coupling through clay supported palladium complexes with tridentate pincer bis-carbene ligands

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Cited by 72 publications
(31 citation statements)
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“…It is worth pointing out that other small size phosphite ligands, such as triphenylphosphite, do not yield ortho-metallated complexes under the same reaction conditions [4d,14]. 13 C NMR analysis showed a signal at d 150.1 ppm, which is very typical for the C ipso of CePd s-bonds in ortho-metallated complexes [4,5,14].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…It is worth pointing out that other small size phosphite ligands, such as triphenylphosphite, do not yield ortho-metallated complexes under the same reaction conditions [4d,14]. 13 C NMR analysis showed a signal at d 150.1 ppm, which is very typical for the C ipso of CePd s-bonds in ortho-metallated complexes [4,5,14].…”
Section: Resultsmentioning
confidence: 99%
“…This method provides an entry to arylphosphonates, arylphosphinates and arylphosphine oxides [10]. To the best of our knowledge, pincer complexes have not been studied in CeP cross-coupling reactions for the preparation of tertiary phosphine-boranes, though, their remarkable catalytic performances in Heck [11], Suzuki [12] and Sonogashira [13] reactions have been carefully studied and are well documented.…”
Section: Introductionmentioning
confidence: 99%
“…Scheme 42. Similar heterogenized catalytic systems were tested in the Sonogashira coupling of aryl halides with phenylacetylene (Scheme 41). [94] The activities of the immobilized systems are higher than that of previously reported Pd-carbene catalysts [95] or Pd-immobilized catalytic systems [96] for the coupling of the same substrates.…”
Section: Heck and Related C-c Bond Formation Reactionsmentioning
confidence: 65%
“…[75][76][77] Peris and Claver et al have immobilized the rigid pincer complexes, type 27 ( Figure 4), in clays (montmorillonite and bentonite), and tested the resulting systems in the Heck olefination of aryl halides and Sonogashira coupling of aryl halides with terminal alkynes. [76,77] In the first example, Peris and Claver et al, employed the catalyst system to couple phenyl iodide and styrene at temperatures of 180°C and recycled the system up to 10 times with little loss in activity. [76] Aryl bromides could also be coupled with good yields.…”
Section: Cross-coupling Reactions (Ni Pd)mentioning
confidence: 99%