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Ni-Catalyzed electrophile driven regioselective arylative cyclization of ortho-functional diaryl acetylenes for the synthesis of pyridine and indene derivatives
Organic Chemistry Frontiers ( IF 5.4 ) Pub Date : 2019-11-18 , DOI: 10.1039/c9qo01266d
Maneesh Kumar Reddy Singam 1, 2, 3, 4, 5 , Attunuri Nagireddy 1, 2, 3, 4, 5 , Manda Rajesh 1, 2, 3, 4, 5 , Veeramalla Ganesh 1, 2, 3, 4, 5 , Maddi Sridhar Reddy 1, 2, 3, 4, 5
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A regioselective carbonickelation followed by cyclization, an arylative cyclization, of ortho functional diaryl acetylenes is achieved apparently through an electrophile driven alkyne polarization. A series of selectively substituted di aryl isoquinoline, pyridine and indene derivatives are thus accessed from diarylacetylenes with azide, carbonyl and cyanide tethers.

中文翻译:

镍催化亲电的邻官能二芳基乙炔的区域选择性芳基化环化反应,用于合成吡啶和茚衍生物

显然,通过亲电试剂驱动的炔烃极化,可以实现官能二芳基乙炔的区域选择性羰基化,环化,芳基环化。因此,可以从二芳基乙炔与叠氮化物,羰基和氰化物系链中获得一系列选择性取代的二芳基异喹啉,吡啶和茚衍生物。
更新日期:2019-11-18
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