Cross-dehydrogenative coupling of α-C(sp3)-H of ethers/alkanes with C(sp2)-H of heteroarenes under metal-free conditions

被引:55
|
作者
Ambala, Srinivas [1 ,2 ]
Thatikonda, Thanusha [1 ,2 ]
Sharma, Shweta [1 ]
Munagala, Gurunadham [1 ,2 ]
Yempalla, Kushalava Reddy [1 ,2 ]
Vishwakarma, Ram A. [1 ,2 ]
Singh, Parvinder Pal [1 ,2 ]
机构
[1] CSIR, Indian Inst Integrat Med, Div Med Chem, Jammu 180001, India
[2] Acad Sci & Innovat Res, Jammu 180001, India
关键词
ALPHA-OXYALKYLATION; CYCLIC ETHERS; FUNCTIONALIZATION; ESTERIFICATION; QUINOLINES; THIOLATION; RADICALS; ALKANES; BONDS;
D O I
10.1039/c5ob01268f
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Here we have developed an effective metal-free dehydrogenative coupling method wherein alpha-oxyalkyl and alkyl radicals were generated from various ethers and alkanes to undergo coupling with a variety of electron-deficient heteroarenes such as un/substituted iso-quinolones, quinolines, pyridines, pyrazines and pyrimidines. The persulfate-acetone-water system was optimized for the dehydrogenative coupling with cyclic ethers which gave moderate to excellent yields of alpha-oxyalkyl containing heteroarenes. We have also optimized the conditions for coupling with cyclic alkanes and alicyclic ethers and demonstrated by conducting the reactions with a variety of electron-deficient heteroarenes. Further, the present method is also applicable to electron deficient arenes like naphthoquinones and moreover, it didn't require any external acid.
引用
收藏
页码:11341 / 11350
页数:10
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