70912-54-8Relevant articles and documents
Synthesis of [1,2-A]-fused tricyclic dihydroquinolines by palladiumcatalyzed intramolecular C-N cross-coupling of polarized heterocyclic enamines
Bro?, B?etislav,R??i?ková, Zdeňka,?im?nek, Petr
, p. 118 - 141 (2016/10/22)
A simple methodology for [1,2-A]-fused tricyclic dihydroquinolines is established. The key ste of the methodology is an intramolecular Buchwald-Hartwig amination reaction of suitabl halogenated (both bromo and chloro) cyclic enaminoketones, enaminoesters and enaminonitrile with various ring size (from five-to seven-membered). Optimal reaction conditions (palladiu source, base, ligand) depend on the ring size of the starting enamine, giving 65-98% yield of th tricyclic product. A treatment of the products with perchloric acid gives respective quinoliniu perchlorates.
Reaction des carbanions maloniques sur le S-methyl ε-thiocaprolactime
Lhommet, Gerard,Richaud, Marie, Genevieve,Maitte, Piere
, p. 431 - 432 (2007/10/02)
S-Methyl-ε-thiocaprolactim reacted with methylene compounds such as β-diketones, β-keto esters or some malonates.We have shown that S-methyl-ε-thiocaprolactim is a more satisfactory activated form of the amide than O-methyl-ε-caprolactim.
