参考标题:Synthesis Of The 2H-Quinolizin-2-One Scaffold Via A Stepwise Acylation-Intramolecular Annulation Strategy 作者:Swaminathan R. Natarajan,Meng-Hsin Chen,Stephen T. Heller,Robert M. Tynebor,Ellen M. Crawford,Cui Minxiang,Han Kaizheng,Jingchao Dong,Bin Hu,Wu Hao,Shu-Hui Chen |发布日期:2006.7 摘要:A Rapid Entry Into The 2H-Quinolizin-2-One Starting From 2-Alkyl Pyridine Has Been Developed. Initial Deprotonation Of A 2-Alkyl Pyridine Followed By Acylation With A β-Tms-Propyonate Derivative Provides Acyclic Precursors That After Deprotection Undergoes A 6-Endo-Trig Cyclization To Yield The Desired 2H-Quinolizin-2-One Derivative. This Synthetic Strategy Was Found To Be Generally Applicable As Evidenced
合成参考文献
摘要:Aguilar, E.; López, L. A., Science of Synthesis Knowledge Updates, (2014) 2, 101. 摘要:Harris, P. A., Science of Synthesis: Knowledge Updates, (2024) 1, 38.