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Palladium-Catalyzed Intermolecular Aminocarbonylation of Alkenes: Efficient Access of beta-Amino Acid Derivatives
Alternative Title钯催化烯烃的分子内胺羰基化反应: 高效合成β-氨基酸衍生物
Cheng JS(程家顺); Qi XX(亓晓旭); Li M(李明); Chen PH(陈品红); Liu GS(刘国生)
2015
Source PublicationJ. Am. Chem. Soc.
Volume137Issue:7Pages:2480-2483
AbstractA novel palladium-catalyzed intermolecular aminocarbonylation of alkenes has been developed in which the employment of hypervalent iodine reagent can accelerate the intermolecular aminopalladation, which thus provides the successful catalytic transformation. The current transformation presents one of the most convenient methods to generate beta-amino acid derivatives from simple alkenes.
Subtype论文
Subject Area金属有机化学
DOI10.1021/jacs.5600719
URL查看原文
Indexed BySCI
Language英语
WOS IDWOS:000350192700018
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Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/39579
Collection金属有机化学国家重点实验室
Corresponding AuthorLiu GS(刘国生)
Affiliation中科院上海有机化学研究所, 金属有机化学国家重点实验室
Recommended Citation
GB/T 7714
Cheng JS,Qi XX,Li M,et al. Palladium-Catalyzed Intermolecular Aminocarbonylation of Alkenes: Efficient Access of beta-Amino Acid Derivatives[J]. J. Am. Chem. Soc.,2015,137(7):2480-2483.
APA 程家顺,亓晓旭,李明,陈品红,&刘国生.(2015).Palladium-Catalyzed Intermolecular Aminocarbonylation of Alkenes: Efficient Access of beta-Amino Acid Derivatives.J. Am. Chem. Soc.,137(7),2480-2483.
MLA 程家顺,et al."Palladium-Catalyzed Intermolecular Aminocarbonylation of Alkenes: Efficient Access of beta-Amino Acid Derivatives".J. Am. Chem. Soc. 137.7(2015):2480-2483.
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