化学
甲酰化
戊烯
背景(考古学)
胺气处理
衍生工具(金融)
组合化学
替代(逻辑)
有机化学
分子
催化作用
古生物学
计算机科学
金融经济学
经济
生物
程序设计语言
作者
Enikő Meiszter,Tamás Gazdag,Péter J. Mayer,Attila Kunfi,Tamás Holczbauer,Máté Sulyok‐Eiler,Gábor London
标识
DOI:10.1021/acs.joc.3c02564
摘要
Stable azaheterocyclic derivatives of pentalene have been reported by the group of Hafner in the 1970s. However, these structures remained of low interest until recently, when they started to be investigated in the context of organic light-emitting diodes' (OLEDs') development. Herein, we revisit the synthesis of stable azapentalene derivative 1,3-bis(dimethylamino)-2-azapentalene and further explore its properties both computationally and experimentally. Beyond the reproduction and optimization of some previously reported transformations, such as formylation and amine substitution, the available scope of reactions was expanded with azo-coupling, selective halogenations, and cross-coupling reactions.
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