...
首页> 外文期刊>The Journal of Organic Chemistry >A Study on the Asymmetric Synthesis of β-Lactams through Double Stereodifferentiating Cycloaddition Reactions
【24h】

A Study on the Asymmetric Synthesis of β-Lactams through Double Stereodifferentiating Cycloaddition Reactions

机译:双立体差示环加成反应不对称合成β-内酰胺的研究

获取原文
获取原文并翻译 | 示例
           

摘要

The cycloaddition reaction of chiral aminoketenes, generated from their corresponding acid chlorides and triethylamine, with chiral imines is evaluated as the most direct approach for the construction of cis-β-lactams with the absolute stereochemistry at the C_3 and C_4 positions being controlled by the ketene partner, independently of the absolute stereochemistry of the imine component.
机译:由其相应的酰氯和三乙胺产生的手性氨基酮烯与手性亚胺的环加成反应被认为是构建顺式-β-内酰胺的最直接方法,其中C_3和C_4位置的绝对立体化学受烯酮控制伴侣,与亚胺成分的绝对立体化学无关。

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