合成目标产物 3-(1-Naphthoyl)Indole 主要起始原料 Indole And 1-Naphthoyl Chloride
(文献来源)合成步骤主要原料 Indole 和 1-Naphthoyl Chloride
吲哚置于乙醚,乙基溴化镁体系中,化学反应生成3-(1-萘甲酰基)吲哚 参考文献:Buu-Hoi Et Al.,Journal Of The Chemical Society,1957,P. 625,627 标题:Buu-Hoi Et Al.,Journal Of The Chemical Society,1957,P. 625,627
参考标题:A Novel Synthesis OfN-Hydroxy-3-Aroylindoles And 3-Aroylindoles 作者:Gabriella Ieronimo,Giovanni Palmisano,Angelo Maspero,Alessandro Marzorati,Luca Scapinello,Norberto Masciocchi,Giancarlo Cravotto,Alessandro Barge,Marco Simonetti,Keshav Lalit Ameta,Kenneth M. Nicholas,Andrea Penoni 摘要:A Straightforward Indole Synthesis Via Annulation Of C-Nitrosoaromatics With Conjugated Terminal Alkynones Was Realised Achieving A Simple, Highly Regioselective, Atom- And Step Economical Access To 3-Aroylindoles In Moderate To Good Yields. Further Functionalizations Of Indole Scaffolds Were Investigated And An Easy Way To Jwh-018, A Synthetic Cannabinoid, Was Achieved.
合成参考文献
参考文献:10.1186/1758-2946-6-22 摘要:Krasowski MD, Ekins S. Using cheminformatics to predict cross reactivity of “designer drugs” to their currently available immunoassays. Journal of Cheminformatics. 2014 May 10;6(1):22. doi: 10.1186/1758-2946-6-22.