2006
DOI: 10.1016/j.jfluchem.2005.09.003
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Efficient synthesis of fluorinated biphenyl derivatives via Pd-catalyzed Suzuki coupling reactions in aqueous solvents at room temperature

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Cited by 27 publications
(14 citation statements)
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“…Also, the coupling reaction could be efficiently executed with aryl boronic acids containing electron-donating and electron-withdrawing groups (Table 3, entries 1, 9 and 10). And the coupling of aryl iodides with phenyl boronic acid gave excellent yields (Table 3, entries [11][12][13][14]. We also performed the reaction with aryl chlorides in our system.…”
Section: Resultsmentioning
confidence: 91%
See 1 more Smart Citation
“…Also, the coupling reaction could be efficiently executed with aryl boronic acids containing electron-donating and electron-withdrawing groups (Table 3, entries 1, 9 and 10). And the coupling of aryl iodides with phenyl boronic acid gave excellent yields (Table 3, entries [11][12][13][14]. We also performed the reaction with aryl chlorides in our system.…”
Section: Resultsmentioning
confidence: 91%
“…In general, these reactions were carried out in the presence of a variety of phosphine based ligands [12][13][14]. Lately, N-heterocyclic carbenes (NHCs), as a substitute of phosphorus-containing ligands [15,16], have been introduced as potentially effective ligands for Suzuki cross-coupling reactions.…”
Section: Introductionmentioning
confidence: 99%
“…There has been some interest in the cross-coupling of fluorinated nucleophiles due to the application of fluoroaryl substituents in medicinal chemistry and in liquid crystals. [30-34] The Buchwald group recently reported the first couplings of such substrates with aryl chlorides in high yield. [12] Using our catalyst system, it was pleasing that good yields were also observed with 2 , 3 and 4 substituted fluorophenyl boronic acids but within just 10 minutes of reaction time (Table 1: Entries 6, 8, and 10).…”
Section: Resultsmentioning
confidence: 99%
“…In addition, the liquid crystalline materials containing monofluoro-, difluoro-or trifluoro-substituted phenyls [15][16][17][18][19][20] are the most prominent for application in thin-film transistor liquid crys- tal displays (TFT-LCDS). The long, lath-like molecular structure of most fluorinated liquid crystalline compounds demanded by thin-film transistor liquid crystal displays makes Suzuki cross-coupling reactions very important in synthesis.…”
Section: Catalytic Activitymentioning
confidence: 99%