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Wagner Meerwein rearrangement of [3.3.1] bicyclic N-Boc aminols: vinyl migration in preference to aryl migration
Alternative TitleWagner 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
Source PublicationTetrahedron
Volume70Issue:44Pages:8374-8379
AbstractThe 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.
Subject Area天然产物有机化学
DOI10.1016/j.tet.2014.08.072
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Indexed BySCI
Language英语
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Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/38990
Collection中科院天然产物有机化学重点实验室
Affiliation中科院上海有机化学研究所
Recommended Citation
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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