WebMar 28, 2024 · The reaction tolerates various substituted pivalophenone N-H imines as well as cyclic and acyclic alkenyl phosphates. Discover the world's research. 20+ million members; 135+ million publications; WebA cobalt-catalyzed ortho-C–H benzylation reaction of pivalophenone N–H imines with benzyl phosphates is reported. The reaction is promoted at room temperature by a ternary catalytic system comprising Co(acac)3, a pyridylphosphine ligand, and a Grignard reagent and tolerates a series of substituted pivalophenone imines and benzyl phosphates to …
Pivalophenone imine as a benzonitrile surrogate for directed C-H …
WebMay 14, 2024 · Pivalophenone N−H imines and triethylsilane undergo dehydrogenative C−Si bond formation in the presence of [Fe3(CO)12] and norbornene, affording ortho‐silylated products in moderate yields. WebMay 30, 2024 · Pivalophenone N–H imine undergoes facile directed C–H functionalization and subsequent iminyl radical fragmentation, thus efficiently affording ortho … grant all on all tables
Iron-Catalyzed ortho C-H Arylation and Methylation of Pivalophenone …
WebMay 14, 2024 · Pivalophenone N−H imine undergoes ortho C−H silylation with triethylsilane in the presence of [Fe 3 (CO) 12] as a catalyst and norbornene as a hydrogen acceptor. The product can be readily transformed into ortho -silylated benzonitrile via conversion of the imine functionality to a cyano group under peroxide photolysis. WebBuilding on the above background, we have found that pivalophenone N–H imine serves as a benzonitrile surrogate for directed C–H functionalization reactions under cobalt … WebA new series of polyester pyrazolopyridophanes of cyclic 5-7 and acyclic structure 8 has been synthesized. The larger cyclic receptors 6 (36-membered) and 7 (48-membered) … grant all in redshift