Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives

被引:16
|
作者
Liu, Xiangyu [1 ]
Wu, Chengjuan [1 ]
Zhang, Jing [1 ]
Shi, Yihan [1 ]
Zhang, Shengnan [1 ]
Geng, Yan [2 ]
Tung, Chen-Ho [1 ]
Wang, Wenguang [1 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Minist Educ, Key Lab Colloid & Interface Chem, 27 South Shanda Rd, Jinan 250100, Shandong, Peoples R China
[2] Shandong Normal Univ, Coll Chem Chem Engn & Mat Sci, Jinan 250014, Shandong, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2018年 / 5卷 / 20期
基金
中国国家自然科学基金;
关键词
C BOND FORMATION; TRANSITION-METAL-FREE; OXIDATIVE CYCLIZATION; BIPHENYL ISOCYANIDES; EFFICIENT SYNTHESIS; N-ARYLACRYLAMIDES; ARYL ISONITRILES; CARBENE RADICALS; H BOND; 2-ISOCYANOBIPHENYLS;
D O I
10.1039/c8qo00887f
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A neutral cobalt(ii) compound Cp*Co(1,2-Ph2PC6H4S) (1, Cp* = Me5C5-) catalyzes the radical cyclization of 2-isocyano-biphenyls with alkyl halides, providing a variety of 6-substituted phenanthridines and phenanthridine-fused polycyclic compounds in good to excellent yields. The mild reaction conditions allow the catalysis to tolerate various alkyl halides for scaled-up syntheses. Polycyclic compounds with a 6-ethylpropanoate group at the C6 position can be hydrolyzed to provide the 6-ethyl substituted N-heterocycles, which exhibit useful emission properties upon protonation.
引用
收藏
页码:2997 / 3002
页数:6
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