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Intermolecular sequential [4+2]-cycloaddition-aromatization reaction of aryl-substituted allenes with DMAD affording phenanthrene and naphthalene derivatives
其他题名Intermolecular sequential [4+2]-cycloaddition-aromatization reaction of aryl-substituted allenes with DMAD affording phenanthrene and naphthalene derivatives
Jiang XF(姜雪峰); Kong WQ(孔望清); Chen J(陈洁); Ma SM(麻生明)
2008
发表期刊Org. Biomol. Chem.
ISSN1477-0520
卷号6期号:19页码:3606-3610
摘要An efficient entry to phenanthrene and naphthalene derivatives through intermolecular sequential [4 + 2]-cycloaddition-aromatization reactions of aryl-substituted allenes with DMAD in the absence of any catalyst was discovered. Ill this reaction the aromatic ring and the adjacent carbon-carbon double bond of the allene unit acted as the 1,3-diene.
学科领域有机化学
部门归属上海有机所; 浙江大学
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收录类别SCI
语种英语
WOS记录号WOS:000259813400021
引用统计
被引频次:22[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.sioc.ac.cn/handle/331003/12156
专题金属有机化学国家重点实验室
通讯作者Ma SM(麻生明)
推荐引用方式
GB/T 7714
Jiang XF,Kong WQ,Chen J,et al. Intermolecular sequential [4+2]-cycloaddition-aromatization reaction of aryl-substituted allenes with DMAD affording phenanthrene and naphthalene derivatives[J]. Org. Biomol. Chem.,2008,6(19):3606-3610.
APA 姜雪峰,孔望清,陈洁,&麻生明.(2008).Intermolecular sequential [4+2]-cycloaddition-aromatization reaction of aryl-substituted allenes with DMAD affording phenanthrene and naphthalene derivatives.Org. Biomol. Chem.,6(19),3606-3610.
MLA 姜雪峰,et al."Intermolecular sequential [4+2]-cycloaddition-aromatization reaction of aryl-substituted allenes with DMAD affording phenanthrene and naphthalene derivatives".Org. Biomol. Chem. 6.19(2008):3606-3610.
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