C–N Bond Formation from Allylic Alcohols via Cooperative Nickel and Titanium Catalysis
作者:S. Hadi Nazari、Norma Tiempos-Flores、Kelton G. Forson、Jefferson E. Bourdeau、David J. Michaelis
DOI:10.1021/acs.joc.8b01474
日期:2018.9.7
Amination of allylicalcohols is facilitated via cooperative catalysis. Catalytic Ti(O-i-Pr)4 is shown to dramatically increase the rate of nickel-catalyzed allylic amination, and mechanistic experiments confirm activation of the allylicalcohol by titanium. Aminations of primary and secondary allylicalcohols are demonstrated with a variety of amine nucleophiles. Diene-containing substrates also cyclize
Palladium catalyzed intermolecular hydroamination of 1-substituted allenes: an atom-economical method for the synthesis of N-allylamines
作者:John F. Beck、Danielle C. Samblanet、Joseph A. R. Schmidt
DOI:10.1039/c3ra43870h
日期:——
linear products could be formed selectively in the hydroamination of p-fluorophenylallene with alkyl amines through careful control of [(3IPtBu)Pd(allyl)]OTf catalyst loading and reaction duration. Overall, the branched allylamines produced are useful synthetic intermediates due to their available unsaturated vinyl group, while the linear allylamine products are chemically similar to a class of known pharmaceuticals