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Synthesis of indolizine derivatives containing eight-membered rings via a gold-catalyzed two-fold hydroarylation of diynes
Chemical Communications ( IF 4.9 ) Pub Date : 2018-01-08 00:00:00 , DOI: 10.1039/c7cc09250d
Ruixing Liu 1, 2, 3, 4, 5 , Qiang Wang 1, 2, 3, 4, 5 , Yin Wei 1, 2, 3, 4, 5 , Min Shi 1, 2, 3, 4, 5
Affiliation  

A gold-catalyzed method for the construction of indolizines with eight-membered rings has been developed. The reaction proceeded through a two-fold hydroarylation with indole or pyrrole derivatives containing a 1,6-diyne using a tri(1-adamantyl)phosphine gold complex as the catalyst, affording 1,8-disubstituted indolizines in moderate to good yields in DCE at 80 °C. The potential usefulness of these indolizines as blue or green OLEDs has been also disclosed.

中文翻译:

通过金催化的二炔二元氢芳基化反应合成含八元环的吲哚嗪衍生物

已经开发了一种金催化的八元环吲哚嗪的构建方法。该反应通过使用三(1-金刚烷基)膦金络合物作为催化剂,与含有1,6-二炔的吲哚或吡咯衍生物进行两次氢化芳基化反应,在DCE中得到中等至良好收率的1,8-二取代的吲哚并嗪在80°C下。还已经公开了这些吲哚嗪作为蓝色或绿色OLED的潜在用途。
更新日期:2018-01-31
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