首页> 美国卫生研究院文献>ChemistryOpen >Metal Catalysis in Thiolation and Selenation Reactions of Alkynes Leading to Chalcogen‐Substituted Alkenes and Dienes
【2h】

Metal Catalysis in Thiolation and Selenation Reactions of Alkynes Leading to Chalcogen‐Substituted Alkenes and Dienes

机译:炔烃的硫代和硒代反应中的金属催化生成硫属元素取代的烯烃和二烯

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。
获取外文期刊封面目录资料

摘要

This review covers recent achievements in metal‐catalyzed Z−H and Z−Z (Z=S, Se) bond addition to the triple bonds of alkynes—a convenient and atom‐efficient way to carbon‐element bond formation. Various catalytic systems (both homogeneous and heterogeneous) developed to date to obtain mono‐ and bis‐chalcogen‐substituted alkenes or dienes, as well as carbonyl compounds or heterocycles, starting from simple and available alkynes and chalcogenols or dichalcogenides are described. The right choice of metal and ligands allows us to perform these transformations with high selectivities under mild reaction conditions, thus tolerating unprotected functional groups in substrates and broadening ways of further modification of the products. The main aim of the review is to show the potential of the catalytic methods developed in synthetic organic chemistry. Thus, emphasis is made on the scope of reactions, types of products that can be selectively formed, convenience, and scalability of the catalytic procedures. A brief mechanistic description is also given to introduce new readers to the topic.
机译:这篇综述涵盖了在炔烃的三键上金属催化的ZH和ZZ(Z = S,Se)键加成方面的最新成就-一种便捷且原子高效的碳元素键形成方法。迄今为止,已开发了各种催化系统(均相和非均相),以从单和可用的炔烃,硫属元素醇或二卤化物开始获得单硫醇盐和双硫属元素取代的烯烃或二烯,以及羰基化合物或杂环。正确选择金属和配体可以使我们在温和的反应条件下以高选择性进行这些转化,从而可以耐受底物中未保护的官能团,并拓宽了产品进一步修饰的途径。综述的主要目的是显示合成有机化学中开发的催化方法的潜力。因此,重点放在反应范围,可选择性形成的产物类型,便利性和催化方法的可扩展性上。还给出了简短的机械描述,以向新读者介绍该主题。

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