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A palladium-catalyzed decarboxylative (5 + 5) cyclization reaction of vinyloxazolidine-2,4-diones: access to ten-membered N,O-containing heterocycles
Organic Chemistry Frontiers ( IF 4.6 ) Pub Date : 2024-06-04 , DOI: 10.1039/d4qo00609g
Xiao-Hui Fu 1, 2, 3 , Juan Liao 1, 2, 3 , Zhen-Hua Wang 2 , Zhen-Zhen Ge 1, 2, 3 , Ming-Qiang Zhou 1, 2, 3 , Yong You 2 , Yan-Ping Zhang 2 , Jian-Qiang Zhao 2 , Ji-Hong Lu 4 , Wei-Cheng Yuan 1, 2, 3
Affiliation  

This study describes a palladium-catalyzed decarboxylative (5 + 5) cyclization reaction of vinyloxazolidine-2,4-diones. The cyclization between aza-π-allylpalladium and oxa-π-allylpalladium intermediates, both in situ generated from vinyloxazolidine-2,4-diones, is successfully realized to produce a series of ten-membered N,O-containing heterocycles in up to 90% yield. This work represents a pioneering application of vinyloxazolidine-2,4-diones as oxa-π-allylpalladium species precursors for the construction of heterocyclic compounds.

中文翻译:


乙烯基恶唑烷-2,4-二酮的钯催化脱羧(5 + 5)环化反应:获得十元含 N,O 杂环



本研究描述了乙烯基恶唑烷-2,4-二酮的钯催化脱羧 (5 + 5) 环化反应。氮杂-π-烯丙基钯和氧杂-π-烯丙基钯中间体(均由乙烯基恶唑烷-2,4-二酮原位生成)之间的环化已成功实现,可产生一系列高达 90 的十元含 N,O 杂环。 % 屈服。这项工作代表了乙烯基恶唑烷-2,4-二酮作为氧杂-π-烯丙基钯物质前体用于构建杂环化合物的开创性应用。
更新日期:2024-06-04
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