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InChI
1S/C14H23P.C8H11N.C5H5.ClH.Fe.Pd/c1-3-11-5-9(1)7-13(11)15-14-8-10-2-4-12(14)6-10;1-9(2)7-8-5-3-4-6-8;1-2-4-5-3-1;;;/h9-15H,1-8H2;3-5H,7H2,1-2H3;1-5H;1H;;/q;;;;;+1/p-1/t9-,10+,11+,12-,13?,14?;;;;;
SMILES string
[Fe].[CH]1[CH][CH][CH][CH]1.CN(C)C[C]2[CH][CH][CH][C]2[Pd]Cl.[H][C@]34CC[C@]([H])(C3)C(C4)PC5C[C@]6([H])CC[C@@]5([H])C6
InChI key
WLPBCKROBGAVNZ-HHYUVNRKSA-M
assay
≥97.0% (C)
form
powder
reaction suitability
core: palladium, reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Cross Couplings, reaction type: Heck Reaction, reaction type: Hiyama Coupling, reaction type: Negishi Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Suzuki-Miyaura Coupling, reagent type: catalyst
mp
~156 °C (dec.), ~156 °C
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Articles
Palladacyclic catalysts by Bedford's group facilitate coupling reactions with low catalyst loadings and challenging aryl chlorides.
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