Suppr超能文献

通过自由基引发的去芳构化螺环化反应电化学合成螺[4.5]三烯酮。

Electrochemical Synthesis of Spiro[4.5]trienones through Radical-Initiated Dearomative Spirocyclization.

机构信息

College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, 30 Puzhu Rd S., Nanjing, 211816, P.R. China.

College of Engineering, China Pharmaceutical University, 24 Tongjiaxiang, Nanjing, 210003, P.R. China.

出版信息

ChemSusChem. 2020 Apr 21;13(8):2053-2059. doi: 10.1002/cssc.202000098. Epub 2020 Mar 12.

Abstract

A novel and green route has been developed for the electrochemical synthesis of spiro[4.5]trienones through radical-initiated dearomative spirocyclization of alkynes with diselenides. This metal-free and oxidant-free electrosynthesis reaction was performed in an undivided cell under mild conditions. A variety of selenation spiro[4.5]trienones products were prepared in moderate-to-good yields, showing a broad scope and functional group tolerance. Moreover, the developed continuous-flow system combined with electrosynthesis possesses the potential to achieve scaled-up reactions, overcoming the low efficiency of conventional electrochemical scaled-up reactions.

摘要

一种新颖且绿色的电化学方法已被开发出来,用于通过炔烃与二硒醚的自由基引发的去芳构化螺环化反应来电化学合成螺[4.5]三烯酮。这种无金属和无氧化剂的电合成反应在温和条件下在一个不分流的电池中进行。多种硒代螺[4.5]三烯酮产物以中等至良好的收率制备,显示出广泛的范围和官能团耐受性。此外,所开发的连续流系统与电合成相结合,具有实现规模化反应的潜力,克服了传统电化学规模化反应效率低的问题。

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