Palladium-Catalyzed C-H Functionalization of Phenyl 2-Pyridylsulfonates.

Title Palladium-Catalyzed C-H Functionalization of Phenyl 2-Pyridylsulfonates.
Authors B. Li; D.D. Guo; S.H. Guo; G.F. Pan; Y.R. Gao; Y.Q. Wang
Journal Chem Asian J
DOI 10.1002/asia.201601413
Abstract

An efficient palladium(II)-catalyzed intermolecular direct ortho-alkenylation and acetoxylation of phenols has been developed. The reaction proceeded via a seven-membered cyclopalladated intermediate and showed complete regio- and diastereoselectivity. The approach also provided an efficient route for the synthesis of coumarins and benzofurans.

Citation B. Li; D.D. Guo; S.H. Guo; G.F. Pan; Y.R. Gao; Y.Q. Wang.Palladium-Catalyzed C-H Functionalization of Phenyl 2-Pyridylsulfonates.. Chem Asian J. 2017;12(1):130144. doi:10.1002/asia.201601413

Related Elements

Palladium

Palladium Bohr ModelSee more Palladium products. Palladium (atomic symbol: Pd, atomic number: 46) is a Block D, Group 10, Period 5 element with an atomic weight of 106.42. The number of electrons in each of palladium's shells is 2, 8, 18, 18 and its electron configuration is [Kr] 4d10. The palladium atom has a radius of 137 pm and a Van der Waals radius of 202 pm. In its elemental form, palladium has a silvery white appearance. Palladium is a member of the platinum group of metals (along with platinum, rhodium, ruthenium, iridium and osmium). Elemental PalladiumPalladium has the lowest melting point and is the least dense of the group. Palladium can be found as a free metal and alloyed with other platinum-group metals. Nickel-copper deposits are the main commercial source of palladium. Palladium was discovered and first isolated by William Hyde Wollaston in 1803. Its name is derived from the asteroid Pallas.

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