1990
DOI: 10.1002/9780470132593.ch28
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Tetrakis(Triphenylphosphine)Palladium(0)

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Cited by 88 publications
(26 citation statements)
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“…n‐ Buthyllithium solution (2.4 m in hexanes) was purchased from J&K Scientific Ltd. Potassium carbonate was purchased from Alfa Aesar. 2,3‐Dibromo‐benzo[ b ]thiophene, 3‐bromo‐2‐(thiophen‐2‐yl)benzo[ b ]thiophene, Spiro‐Bn , and tetrakis(triphenylphosphine)palladium(0) as catalyst for Suzuki as well as Negishi cross‐coupling and dichlorobis(triphenylphosphine)palladium(II) as catalyst for Sonogashira coupling were synthesized according to the literature procedures with slight modifications. Tetrahydrofuran and dichloromethane for reactions were purified with the PureSolv MD 5 solvent purification system before use.…”
Section: Methodsmentioning
confidence: 99%
“…n‐ Buthyllithium solution (2.4 m in hexanes) was purchased from J&K Scientific Ltd. Potassium carbonate was purchased from Alfa Aesar. 2,3‐Dibromo‐benzo[ b ]thiophene, 3‐bromo‐2‐(thiophen‐2‐yl)benzo[ b ]thiophene, Spiro‐Bn , and tetrakis(triphenylphosphine)palladium(0) as catalyst for Suzuki as well as Negishi cross‐coupling and dichlorobis(triphenylphosphine)palladium(II) as catalyst for Sonogashira coupling were synthesized according to the literature procedures with slight modifications. Tetrahydrofuran and dichloromethane for reactions were purified with the PureSolv MD 5 solvent purification system before use.…”
Section: Methodsmentioning
confidence: 99%
“…The catalyst Pd(PPh 3 ) 4 was synthesized according to a literature reference and stored under argon atmosphere in a refrigerator. 38 Diethyl ether (Et 2 O) was freshly distilled from sodium each time prior to the reaction. Solvent (DME/water, 4:1) employed in Suzuki couplings was always degassed with argon prior to utilization.…”
Section: ■ Experimental Detailsmentioning
confidence: 99%
“…The residue was purified by column chromatography on alumina (ethyl acetate/cyclohexane, 9/1, v/v). (9) To a solution of the appropriate iodinated compound (1.14 mmol) in anhydrous toluene (25 mL), beforehand degassed under argon, were successively added, hexabutylditin (783 mL, 1.55 mmol) and freshly prepared tetrakis(triphenylphosphine) palladium(0) [47] (33 mg, 28.6 mmol). The resulting solution was refluxed for 2e14 h under argon.…”
Section: N-[2-(diethylamino)ethyl]-4-chloro-3-iodobenzamide (3)mentioning
confidence: 99%