Wagner Meerwein rearrangement of [3.3.1] bicyclic N-Boc aminols: vinyl migration in preference to aryl migration
其他题名Wagner Meerwein rearrangement of [3.3.1] bicyclic N-Boc aminols: vinyl migration in preference to aryl migration
FU JIANGUO; DING RUI; SUN BINGFENG; Lin GQ(林国强)
2014
发表期刊Tetrahedron
卷号70期号:44页码:8374-8379
摘要The Wagner-Meerwein rearrangement of [3.3.1] bicyclic N-Boc aminols was established, featuring the migration of the vinyl group instead of the aromatic ring. The structure of the rearrangement product was deduced through extensive spectroscopic studies and confirmed by the synthetic efforts. The scope of the reaction was examined and reasonably good yields were obtained for substrates with alkyl, allyl or benzyl substituent. (C) 2014 Elsevier Ltd. All rights reserved.
学科领域天然产物有机化学
DOI10.1016/j.tet.2014.08.072
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收录类别SCI
语种英语
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文献类型期刊论文
条目标识符http://ir.sioc.ac.cn/handle/331003/38990
专题中科院天然产物有机化学重点实验室
作者单位中科院上海有机化学研究所
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GB/T 7714
FU JIANGUO,DING RUI,SUN BINGFENG,et al. Wagner Meerwein rearrangement of [3.3.1] bicyclic N-Boc aminols: vinyl migration in preference to aryl migration[J]. Tetrahedron,2014,70(44):8374-8379.
APA FU JIANGUO,DING RUI,SUN BINGFENG,&林国强.(2014).Wagner Meerwein rearrangement of [3.3.1] bicyclic N-Boc aminols: vinyl migration in preference to aryl migration.Tetrahedron,70(44),8374-8379.
MLA FU JIANGUO,et al."Wagner Meerwein rearrangement of [3.3.1] bicyclic N-Boc aminols: vinyl migration in preference to aryl migration".Tetrahedron 70.44(2014):8374-8379.
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