1373117-65-7Relevant academic research and scientific papers
Lewis acid catalyzed reactivity switch: Pseudo three-component annulation of nitrosoarenes and (epoxy)styrenes
Purkait, Anisha,Saha, Subhajit,Ghosh, Santanu,Jana, Chandan K.
supporting information, p. 15032 - 15035 (2020/12/22)
A Lewis acid catalyzed annulation reaction via arene functionalization of nitrosoarenes and C-C cleavage of (epoxy)styrene to provide arylquinolines is reported. The Lewis acid catalyst altered the annulation pattern providing arylquinolines instead of oxazolidines. The reaction with styrene resulted in a mixture of 2,4-diarylquinoline and 4-Arylquinoline, while only 3-Arylquinoline was formed from the reaction of epoxystyrene. This journal is
Iodine monobromide catalysed regioselective synthesis of 3-arylquinolines from α-aminoacetophenones and: Trans -β-nitrostyrenes
Gattu, Radhakrishna,Mondal, Santa,Ali, Saghir,Khan, Abu T.
, p. 347 - 353 (2019/01/10)
A simple and efficient method for regioselective synthesis of 3-arylquinolines is described from α-aminoacetophenones and trans-β-nitrostyrenes using 20 mol% iodine monobromide as a catalyst in acetonitrile solvent at 80 °C. The present method involves tandem reaction of α-aminoacetophenones and trans-β-nitrostyrenes, formation of two new C-C bonds and cleavage of one C-C bond in a single step. The salient features of the protocol are metal- and oxidant-free reaction conditions, broad substrate scope, and good yields.
Iron-promoted tandem reaction of anilines with styrene oxides via C-C cleavage for the synthesis of quinolines
Zhang, Yicheng,Wang, Min,Li, Pinhua,Wang, Lei
supporting information; experimental part, p. 2206 - 2209 (2012/06/18)
A novel iron-promoted tandem reaction of anilines with styrene oxides via C-C cleavage and C-H activation has been developed. The reaction utilizes an inexpensive FeCl3 as promoter and is suitable for forming a variety of 3-arylquinolines from
