首页> 美国卫生研究院文献>ACS Omega >Substrate-Controlled Product Divergence: Silver-CatalyzedReaction of Trifluoromethyl Ketones with Terminal Alkynes
【2h】

Substrate-Controlled Product Divergence: Silver-CatalyzedReaction of Trifluoromethyl Ketones with Terminal Alkynes

机译:底物控制的产品差异:银催化三氟甲基酮与末端炔烃的反应

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A distinct dichotomy in product distribution was initially observed in the silver-catalyzed reaction of trifluoromethyl (CF3) ketones with terminal alkynes having two different types of electronic natures. The domino reaction smoothly proceeded almost exclusively with high stereoselectivity with terminal alkynes containing ester groups, whereas alkynylation occurred in good yield when terminal alkynes containing aryl or alkyl groups were present. The results indicated that the electronic nature of terminal alkynes can act as a switch that enables either the domino reaction or alkynylation between terminal alkynes and CF3 ketones.
机译:最初在三氟甲基(CF3)酮与具有两种不同电子性质的末端炔烃的银催化反应中观察到明显的产物分布二分法。在含有酯基的末端炔烃的情况下,多米诺反应几乎完全以高立体选择性顺利进行,而当存在含有芳基或烷基的末端炔烃时,炔基化反应的收率很高。结果表明,末端炔烃的电子性质可以充当开关,从而使末端炔烃与CF3酮之间发生多米诺反应或炔基化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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