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Efficient Synthesis of Heterocyle-Fused beta-Naphthylamines via Intramolecular Addition to a Cyano Group Initiated by Nucleopalladation of Alkynes
Alternative Title炔烃亲核钯化启动的对分子内氰基的加成反应-并杂环的b-萘胺类化合物的有效合成
Xia GQ(夏国钦); Han XL(韩秀玲); Lu XY(陆熙炎)
2014
Source PublicationOrg. Lett.
Volume16Issue:23Pages:6184-6187
AbstractA palladium(II)-catalyzed efficient synthesis of heterocycle-fused beta-naphthylamines was accomplished via nucleophilic addition of a carbonpalladium bond to the intramolecular cyano group initiated by nucleopalladation (oxypalladation or aminopalladation) of alkynes.
Subject Area金属有机化学
DOI10.1021/ol5031074
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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/331003/39137
Collection金属有机化学国家重点实验室
Corresponding AuthorHan XL(韩秀玲); Lu XY(陆熙炎)
Affiliation中科院上海有机化学研究所
Recommended Citation
GB/T 7714
Xia GQ,Han XL,Lu XY. Efficient Synthesis of Heterocyle-Fused beta-Naphthylamines via Intramolecular Addition to a Cyano Group Initiated by Nucleopalladation of Alkynes[J]. Org. Lett.,2014,16(23):6184-6187.
APA 夏国钦,韩秀玲,&陆熙炎.(2014).Efficient Synthesis of Heterocyle-Fused beta-Naphthylamines via Intramolecular Addition to a Cyano Group Initiated by Nucleopalladation of Alkynes.Org. Lett.,16(23),6184-6187.
MLA 夏国钦,et al."Efficient Synthesis of Heterocyle-Fused beta-Naphthylamines via Intramolecular Addition to a Cyano Group Initiated by Nucleopalladation of Alkynes".Org. Lett. 16.23(2014):6184-6187.
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