...
首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Hydroxytetraphenylenes as Chiral Ligands: Application to Asymmetric Darzens Reaction of Diazoacetamide with Aldehydes
【24h】

Hydroxytetraphenylenes as Chiral Ligands: Application to Asymmetric Darzens Reaction of Diazoacetamide with Aldehydes

机译:羟基邻苯基作为手性配体:在二氮杂乙酰乙酰乙酰酰胺与醛的不对称Darzens的应用

获取原文
获取原文并翻译 | 示例
           

摘要

Hydroxytetraphenylenes with rigid conformations are potential candidates for employment as chiral ligands in asymmetric synthesis. Highly diastereo-and enantioselective Darzens reactions between aldehydes and diazo-N, N-dimethylacetamide were found to be catalyzed by a chiral titanium complex formed in situ from Ti(OiPr)(4) and chiral 1,16-dihydroxytetraphenylene, leading to the formation of cis-glycidic amides in moderate to high yields with excellent enantiomeric purities (40-99% yield, up to 99% ee).
机译:具有刚性构象的羟基替视是在不对称合成中作为手性配体的潜在候选者。 发现醛和二甲基乙酰胺之间的高度自对映的和对映选择性的Darzens反应,发现由原位的手性钛配合物从Ti(OIPR)(4)和手性1,16-二羟基对苯基形成,导致形成 CIS-甘蔗酰胺中的中等至高产率,具有优异的对映体纯度(40-99%收率,高达99%EE)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号