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. 2020 Dec 8;5(50):32515–32529. doi: 10.1021/acsomega.0c04706

Table 5. Comparison of the Activity of the New Catalytic System Including Bridged-Bis(NHC)PdBr2 (C1) in Cyclocarbonylative Sonogashira Coupling Reactions of 2-Iodophenol and Alkynes with Literature Data.

refs catalyst co-catalyst/ligand/additive base time (h) yield (%)
(33) PdCL2 (5 mol %) (H13C6)3P+C14H29Br (1.5 g) Et3N 24 64–95
(31) PdCL2 (5 mol %) PPh3 (10 mol %) Et3N 24 35–95
(35) Pd(OAc)2 (5 mol %) DPPF (5 mol %) piperazine 24 30–95
(32) Pd2(dba)3 (1.5 mol %) 1,3,5,7-tetramethyl-2,4,8-trioxa-6-phenyl-6-phosphaadamantane (3 mol %) DBU 0.5 MW 62–95
(40) Pd(Pph3)4 (3 mol %) Ac2O (6 mol %) Et3N   51–82
(38) Pd–NHC–Py (0.5 mol %) imidazole (0.5 mol %) pyridine (0.5 mol %) Et2NH 24 25–98
(49) Pd/C (1 mol %)   Et2NH 20 74–98
this work bridged-bis(NHC)PdBr2 (0.5 mol %)   Et2NH 16 53–98