Abstract
Five cross-coupling reactions (named Suzuki, Kumada, Negishi, Stille and Hiyama) were compared in a synthesis of (I, R = Br) with organometallic compd. to give (I, R = Ph). The reactions were carried out in the presence of Pd catalyst (5% by mole), with a molar ratio of the substrates 1:2.5 for 5 h. Treatment of (I, R = Br) with organoborane compd. (Suzuki coupling) gave the highest yields of (I, R = Ph) (21–61%) while with organosilicon compd. (Hiyama coupling) the lowest one (0–5%).
| Translated title of the contribution | Synthesis of 2,5-bis(4-biphenylyl)-1,3,4-oxadiazole with the use of cross-coupling reactions of selected organometallic compounds |
|---|---|
| Original language | Polish |
| Pages (from-to) | 260-263 |
| Number of pages | 4 |
| Journal | Przemysl Chemiczny |
| Volume | 98 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 2019 |
ASJC Scopus subject areas
- General Chemistry
- General Chemical Engineering
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