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

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	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
	2014
发表期刊	Green Chem
卷号	16 页码:4359–4370
文献类型	期刊论文
条目标识符	http://ir.kib.ac.cn/handle/151853/54607
专题	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.