2019
DOI: 10.1080/00397911.2019.1636398
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Synthesis of new 6- and 8-Alkenyl-3,7,3’,4’-Tetramethoxyquercetin derivatives by microwave-assisted Heck coupling

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Cited by 3 publications
(2 citation statements)
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“…Eventually, careful experimentation revealed that the reaction works best using (PCy 3 ) 2 PdCl 2 as the catalyst in toluene at 60 °C in the presence of the base K 3 PO 4 in 41% yield. 22,23 It was found that diene 5 was unstable and should be immediately used in the next step after rapid purification.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
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“…Eventually, careful experimentation revealed that the reaction works best using (PCy 3 ) 2 PdCl 2 as the catalyst in toluene at 60 °C in the presence of the base K 3 PO 4 in 41% yield. 22,23 It was found that diene 5 was unstable and should be immediately used in the next step after rapid purification.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…With PdCl 2 , Pd­(PPh 3 ) 4 , Pd 2 (dba) 3 , and Pd­(OAc) 2 as the palladium catalysts, either no expected product was detected or the reactivity decreased in toluene. Eventually, careful experimentation revealed that the reaction works best using (PCy 3 ) 2 PdCl 2 as the catalyst in toluene at 60 °C in the presence of the base K 3 PO 4 in 41% yield. , It was found that diene 5 was unstable and should be immediately used in the next step after rapid purification.…”
Section: Resultsmentioning
confidence: 99%