Reaktionsgleichung
C1COCCN1.FC(F)(F)c1ccc(Br)cc1>C=[CH](C)->[Pd]1<-[Cl][Pd](<-[Cl]1)<-[CH](=C)C.CC(C)(C)[O-].CC(C)(C)c1ccnc(-c2cc(C(C)(C)C)ccn2)c1.CS(C)=O.[K+]>FC(F)(F)c1ccc(N2CCOCC2)cc1Komponenten
9
Edukt 2
Produkt 3
Reagenzien, Katalysatoren, Lösungsmittel 4
Reaktionsbedingungen
- Temperatur
- 30 °C
Aufarbeitung
- customThe foil sealing tape was removed from the plate.
- addition3 μL of a 0.0667 M solution of caffeine in DMSO was added to each reaction well using an SPT Labtech Mosquito® liquid handling robot
- filtrationThe plates were then centrifuged for 15 to 20 seconds. · liquid-Phase beibehalten
- aliquotFollowing centrifugation, 500 nL of the resultant mixture from each well was carefully dispensed into four 384-well analytical plates (Analytical Sales # 38435) using an SPT Labtech Mosquito® liquid handling robot. Each well of these analytical plates contained 30 μL of DMSO with 0.1% acetic acid, pre-dosed by OpenTrons, to facilitate analysis.
Quellen und Nachweise
- ORD-Eintrag
- ord-0d3e3ef6e20c4fe490bbe33afa464156
- Quelldatensatz
- High-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions
- Originallink
- Quelle ansehen
Verknüpfte Notizen
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