Suppr超能文献

无痕迹 OH 导向 Wacker 氧化消除反应——Wittig 烯烃化/缩合反应的替代方法:从偕丙醇一锅法合成α,β-不饱和和非共轭酮。

Traceless OH-Directed Wacker Oxidation-Elimination, an Alternative to Wittig Olefination/Aldol Condensation: One-Pot Synthesis of α,β-Unsaturated and Nonconjugated Ketones from Homoallyl Alcohols.

机构信息

Department of Chemistry, Indian Institute of Technology Bombay , Powai, Mumbai, 400076 Maharashtra, India.

出版信息

J Org Chem. 2016 Sep 16;81(18):8577-84. doi: 10.1021/acs.joc.6b01899. Epub 2016 Sep 8.

Abstract

A new method for one-pot synthesis of β-substituted and β,β-disubstituted α,β-unsaturated methyl ketones from homoallyl alcohols by sequential PdCl2/CrO3-promoted Wacker process followed by an acid-mediated dehydration reaction has been developed. Remarkably, internal homoallyl alcohols delivered regioselectively nonconjugated unsaturated carbonyl compounds under the same protocol. A new starting material-based synthesis of α,β-unsaturated and nonconjugated methyl ketones is demonstrated.

摘要

一种新的一锅法合成β取代和β,β-二取代α,β-不饱和甲基酮的方法,由偕丙醇通过 PdCl2/CrO3 促进的 Wacker 过程串联酸介导的脱水反应得到。值得注意的是,内部偕丙醇在相同的条件下以区域选择性方式得到非共轭不饱和羰基化合物。展示了一种基于新起始原料的α,β-不饱和和非共轭甲基酮的合成方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验