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Iridium(III)-Catalyzed Difluoroalkylation–Bicyclization of 1,7-Enynes toward Benzo[a]fluoren-5-ones under Visible-Light Photoredox Conditions
Synthesis ( IF 2.6 ) Pub Date : 2020-06-16 , DOI: 10.1055/s-0040-1707863
Wen-Juan Hao 1 , Bo Jiang 1 , Min-Hua Huang 1, 2
Affiliation  


Published as part of the Special Topic Recent Advances in Metal-Catalyzed Ring Construction

Abstract

A new visible-light-induced Ir(III)-catalyzed difluoroalkylation–bicyclization of 1,7-enynes with ethyl 2-bromo-2,2-difluoroacetate (BrCF2CO2Et) is described, furnishing a wide range of difluoromethyl-containing benzo[a]fluoren-5-ones in good to excellent yields. The reaction is operationally simple, proceeds with high efficiency under mild conditions, and shows excellent functional group compatibility.



中文翻译:

铱(III)催化的二氟烷基化-可见光光氧化还原条件下1,7-烯炔向苯并[a]芴-5-酮的双环化


作为特别主题的一部分发表,金属催化环结构的最新进展

抽象

描述了一种新的可见光诱导的Ir(III)催化的2-溴-2,2-二氟乙酸乙酯(BrCF 2 CO 2 Et)对1,7-烯炔的二氟烷基化-双环化,提供了范围广泛的二氟甲基-含苯并[ a ]氟-5-酮,收率良好。该反应操作简单,在温和条件下高效进行,并且显示出优异的官能团相容性。

更新日期:2020-06-16
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