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Ruthenium‐Catalyzed C‐H Arylation and Alkenylation of Furfural Imines with Boronates
European Journal of Organic Chemistry ( IF 2.8 ) Pub Date : 2018-08-10 , DOI: 10.1002/ejoc.201800767
Filipa Siopa 1, 2 , Valérie-Anne Ramis Cladera 1 , Carlos Alberto Mateus Afonso 2 , Julie Oble 1 , Giovanni Poli 1
Affiliation  

Furfural activated again: a Ru‐catalyzed arylation and alkenylation of furfural imines with aryl‐ or alkenyl‐boronates, involving a directed C‐H activation occurring at C3 of the furan ring, was developed. It was revealed that an electron‐rich aromatic imine, such as a p‐dimethylaminophenyl‐imine, enables the coupling with good yields. After the coupling, a smooth hydrolytic removal of the imine directing‐group releases the C3‐functionalized furfurals.
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中文翻译:

钌催化的糠醛亚胺与硼酸酯的CH-H芳基化和烯基化

糠醛再次被活化:开发了Ru催化的糠醛亚胺与芳基或链烯基硼酸酯的芳基化和烯基化反应,涉及在呋喃环的C3处发生直接的CH活化。结果表明,富电子的芳族亚胺,例如二甲氨基苯基亚胺,能够以良好的收率进行偶合。偶联后,平滑水解除去亚胺导向基团,释放出C3功能化的糠醛。
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更新日期:2018-08-10
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