Suppr超能文献

配体控制的区域选择性和对映选择性铜催化炔烃的加氢烯丙基化反应。

Ligand-Controlled Regiodivergent and Enantioselective Copper-Catalyzed Hydroallylation of Alkynes.

机构信息

Jilin Province Key Laboratory of Organic Functional Molecular Design & Synthesis, Department of Chemistry, Northeast Normal University, Changchun, 130024, China.

出版信息

Angew Chem Int Ed Engl. 2017 Oct 9;56(42):13130-13134. doi: 10.1002/anie.201707070. Epub 2017 Sep 12.

Abstract

A ligand-controlled regiodivergent and enantioselective copper-catalyzed intermolecular hydroallylation of alkynes with allylic phosphates and hydrosilanes has been achieved for the first time. The chiral bidentate sulfonate-containing N-heterocyclic carbene ligated CuCl complex leads to enantioenriched S 2'-type products, whereas the use of the IMesCuCl catalyst affords S 2-type products. Thus a range of chiral branched and achiral linear 1,4-dienes could be facilely synthesized from readily available alkynes in a regiodivergent manner.

摘要

首次实现了配体控制的区域和对映选择性铜催化炔烃与烯丙基磷酸酯和硅烷的分子间氢加成反应。手性双齿磺酸盐含氮杂环卡宾配体的 CuCl 配合物导致 S 2'-型产物的对映体过量,而使用 IMesCuCl 催化剂则得到 S 2-型产物。因此,一系列手性支链和非手性线性 1,4-二烯可以通过区域选择性方式从易得的炔烃容易地合成。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验