An environmentally benign, mild, and catalyst-free reaction of quinones with heterocyclic ketene aminals in ethanol: site-selective synthesis of rarely fused [1,2-a]indolone derivatives via an unexpected anti-Nenitzescu strategy

	An environmentally benign, mild, and catalyst-free reaction of quinones with heterocyclic ketene aminals in ethanol: site-selective synthesis of rarely fused [1,2-a]indolone derivatives via an unexpected anti-Nenitzescu strategy
	Bei Zhou
刊名	Green Chem
	2014
卷号	16 页码:4359–4370
内容类型	期刊论文
源URL	[http://ir.kib.ac.cn/handle/151853/54607]
专题	昆明植物研究所_共享文献
推荐引用方式 GB/T 7714	Bei Zhou. An environmentally benign, mild, and catalyst-free reaction of quinones with heterocyclic ketene aminals in ethanol: site-selective synthesis of rarely fused [1,2-a]indolone derivatives via an unexpected anti-Nenitzescu strategy[J]. Green Chem,2014,16:4359–4370.
APA	Bei Zhou.(2014).An environmentally benign, mild, and catalyst-free reaction of quinones with heterocyclic ketene aminals in ethanol: site-selective synthesis of rarely fused [1,2-a]indolone derivatives via an unexpected anti-Nenitzescu strategy.Green Chem,16,4359–4370.
MLA	Bei Zhou."An environmentally benign, mild, and catalyst-free reaction of quinones with heterocyclic ketene aminals in ethanol: site-selective synthesis of rarely fused [1,2-a]indolone derivatives via an unexpected anti-Nenitzescu strategy".Green Chem 16(2014):4359–4370.