Sequential Base-Promoted Formal [4+2] Allenoate Based Cycloaddition: Synthesis of Functionalized Acridines,European Journal of Organic Chemistry

当前位置： X-MOL 学术 › Eur. J. Org. Chem. › 论文详情

Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)

Sequential Base-Promoted Formal [4+2] Allenoate Based Cycloaddition: Synthesis of Functionalized Acridines
European Journal of Organic Chemistry ( IF 2.5 ) Pub Date : 2022-08-05 , DOI: 10.1002/ejoc.202200830
Toktam S. Shirazian ₁ , Hossein Zahedian Tejeneki ₂ , Ali Nikbakht ₁ , Frank Rominger ₃ , Saeed Balalaie ₄

Affiliation

The sequential Michael addition, aldol condensation, and isomerization process in the base-promoted formal [4+2] cycloaddition reaction of (Z)-2-(2-hydroxy-2-alkylvinyl)quinoline-3-carbaldehydes and allenoates provides an effective way to create functionalized acridines under mild conditions.

中文翻译：

顺序碱基促进的形式 [4+2] 烯丙酸酯基环加成：功能化吖啶的合成

( Z )-2-(2-羟基-2-烷基乙烯基)quinoline-3-carbaldehydes 和 allenoates在碱促进的形式 [4+2] 环加成反应中的顺序迈克尔加成、醛醇缩合和异构化过程提供了一种有效的在温和条件下产生官能化吖啶的方法。

更新日期：2022-08-05

点击分享查看原文

点击收藏

阅读更多本刊最新论文本刊介绍/投稿指南11