...
首页> 外文期刊>Science Advances >External oxidant-compatible phosphorus(III)-directed site-selective C–H carbonylation
【24h】

External oxidant-compatible phosphorus(III)-directed site-selective C–H carbonylation

机译:外部氧化剂相容性磷(III) - 重定向位点选择性C-H羰基化

获取原文

摘要

The first development of an external oxidant-compatible system involving a phosphorus(III)-directed C–H functionalization has been uncovered. An efficient C–H esterification of indoles with CO and alcohols has been reported in which the high reactivity and the exclusive C7-selectivity derives from the selection of a P(III)–directing group and the utilization of benzoquinone as an external oxidant with palladium catalysis. This strategy shows many advantages, involving an easily accessible and removable directing group, the use of cheap carbonylation sources, a broad substrate scope, and excellent positional selectivity. Two cyclopalladated intermediates were confirmed by x-ray analysis, uncovering key mechanistic features of this P(III)-directed C–H metalation event.
机译:涉及磷(III) - 共同的C-H官能化的外部氧化剂相容系统的第一次开发已被发现。据报道,具有CO和醇的吲哚的有效C-H酯化,其中高反应性和独占C7选择性来自选择P(III) - 分配组,并利用苯醌作为外部氧化剂与钯的外氧化剂催化。该策略显示了许多优点,涉及易于访问和可移动的直接组,使用廉价的羰基化来源,宽基板范围和优异的位置选择性。通过X射线分析证实了两个环铝化的中间体,揭示了该P(III)的关键机械特征 - 连接的C-H金属化事件。

著录项

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