中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Lithium Diisopropylamide-Mediated Carbolithiation Reactions of Vinylidenecyclopropanes and Further Transformations of the Adducts

文献类型:期刊论文

作者Lu JM(陆建梅) ; Shi M(施敏)
刊名Chem.-Eur. J.
出版日期2009
卷号15期号:24页码:6065-6073
其他题名LDA促进的亚乙烯基环丙烷碳锂化反应和产物的进一步转化
通讯作者施敏
英文摘要Highly stereo- and regioselective carbolithiation reactions of vinylidenecyclopropanes 1 were realized by treatment with lithium diisopropylamide (LDA) in THF and by quenching with various electrophiles such as aryl or aliphatic aldehydes, ketones, enones or propargyl bromide. Transformation of these adducts such as vinylcyclopropenes and allenols was also performed in the presence of Lewis acid or Bronsted acid to provide the fused and conjugated aromatic products in good to high yields under mild conditions.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1002/chem.200900068
语种英语
WOS记录号WOS:000267278900025
公开日期2013-01-09
源URL[http://202.127.28.38/handle/331003/10278]  
专题上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式
GB/T 7714
Lu JM,Shi M. Lithium Diisopropylamide-Mediated Carbolithiation Reactions of Vinylidenecyclopropanes and Further Transformations of the Adducts[J]. Chem.-Eur. J.,2009,15(24):6065-6073.
APA Lu JM,&Shi M.(2009).Lithium Diisopropylamide-Mediated Carbolithiation Reactions of Vinylidenecyclopropanes and Further Transformations of the Adducts.Chem.-Eur. J.,15(24),6065-6073.
MLA Lu JM,et al."Lithium Diisopropylamide-Mediated Carbolithiation Reactions of Vinylidenecyclopropanes and Further Transformations of the Adducts".Chem.-Eur. J. 15.24(2009):6065-6073.

入库方式: OAI收割

来源:上海有机化学研究所

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