2005
DOI: 10.1016/j.tet.2005.09.103
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Synthesis of dendritic oligo(aryl sulfone)s as supports for synthesis

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Cited by 3 publications
(2 citation statements)
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“…BTPS was prepared via a Suzuki coupling reaction of bis(3,5-dichlorophenyl)sulfone with phenylboronic acid using Pd 2 (dba) 3 /PCy 3 /K 3 PO 4 catalyst system in 71% yield. The characterization was established on the basis of 1 H NMR, mass spectrometry, and elemental analysis.…”
mentioning
confidence: 99%
“…BTPS was prepared via a Suzuki coupling reaction of bis(3,5-dichlorophenyl)sulfone with phenylboronic acid using Pd 2 (dba) 3 /PCy 3 /K 3 PO 4 catalyst system in 71% yield. The characterization was established on the basis of 1 H NMR, mass spectrometry, and elemental analysis.…”
mentioning
confidence: 99%
“…Moreover, meta-terphenyls have been used as ligands [10], as intermediates for the synthesis of covalent nanostructures [11] and as electron transporting material [12]. For example, 5′,5′′′′-sulfonyl-di-[1,1′:3′,1′′]-terphenyl (BTPS, Scheme 1), bearing two meta-terphenyl subunits, has been recently prepared from bis (3,5-dichlorophenyl)sulfone [13] by Suzuki-Miyaura coupling in order to develop new highly efficient organic light emitting diodes (OLED) [14]. 2 Pd 2 (dba) 3 Although several procedures allow the synthesis of the terphenyl skeleton, the development of alternative methods is still an issue since the regioselective construction of carbon-carbon bonds is a goal not always easy to be achieved.…”
Section: Introductionmentioning
confidence: 99%