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Synthesis of indene and naphthalene derivatives by a palladium-catalyzed domino carbopalladation/cyclization/coupling process
Department固体润滑国家重点实验室
Guo LN(郭丽娜); Duan XH(段新华); Hu J(胡杰); Bi HP(毕海鹏); Liu XY(刘雪原); Liang YM(梁永民)
2008
Source PublicationEuropean Journal of Organic Chemistry
ISSN1434-193X
Pages1418-1425
AbstractHighly substituted indene and naphthalene derivatives have been readily prepared in good-to-high yields by a palladium-catalyzed domino reaction. This domino reaction involves a Heck carbopalladation/cyclization/coupling process.
KeywordDomino Reactions Carbopalladation Cyclization C-c Coupling
Subject Area材料科学与物理化学
Funding Organizationthe Chinese National Science Foundation (NSF) (NSF- 20621091;NSF-20672049);the “Hundred Scientist Program” of the Chinese Academy of Sciences
Indexed BySCI
Language英语
Citation statistics
Cited Times:22[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/3713
Collection固体润滑国家重点实验室(LSL)
Corresponding AuthorLiang YM(梁永民)
Recommended Citation
GB/T 7714
Guo LN,Duan XH,Hu J,et al. Synthesis of indene and naphthalene derivatives by a palladium-catalyzed domino carbopalladation/cyclization/coupling process[J]. European Journal of Organic Chemistry,2008:1418-1425.
APA 郭丽娜,段新华,胡杰,毕海鹏,刘雪原,&梁永民.(2008).Synthesis of indene and naphthalene derivatives by a palladium-catalyzed domino carbopalladation/cyclization/coupling process.European Journal of Organic Chemistry,1418-1425.
MLA 郭丽娜,et al."Synthesis of indene and naphthalene derivatives by a palladium-catalyzed domino carbopalladation/cyclization/coupling process".European Journal of Organic Chemistry (2008):1418-1425.
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