One-Pot Multicomponent Michael and Thorpe–Ziegler Reaction of Aryl Methyl Ketones
作者:Vikas Jaitak、Bandna、Pralay Das、V. K. Kaul、Bikram Singh、Neeraj Kumar
DOI:10.1080/00397911.2010.515349
日期:2011.9.15
Abstract A regioselective base-promoted Michael and Thorpe–Ziegler reaction between aryl methyl ketones and α,β-unsaturated nitrile was carried out in a single step. Different functional groups in addition to active positions were tolerated under this condition. Results indicated that the reaction proceeds in a consecutive manner as double Michael, triple Michael, and Thorpe–Ziegler condensation. By applying
摘要 芳基甲基酮与 α,β-不饱和腈之间的区域选择性碱基促进 Michael 和 Thorpe-Ziegler 反应一步完成。在这种条件下,除了活性位置外,还可以容忍不同的官能团。结果表明,反应以双迈克尔、三迈克尔和索普-齐格勒缩合的连续方式进行。通过应用点击化学,双迈克尔加合物转化为双四唑,在配位和药物化学中具有广泛的应用。补充材料可用于本文。转至出版商的 Synthetic Communications® 在线版以查看免费的补充文件。