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Palladium-copper-cocatalyzed intramolecular oxidative coupling: an efficient and atom-economical strategy for the synthesis of 3-acylindoles
Department固体润滑国家重点实验室
Xia XF(夏晓峰)1; Zhang, Lu-Lu1; Song XR(宋贤荣)1; Niu YN(牛雁宁)1; Liu XY(刘雪原)1; Liang YM(梁永民)1,2; Liang YM(梁永民)
2013
Source PublicationChemical Communications
ISSN1359-7345
Volume49Issue:14Pages:1410-1412
AbstractA new and efficient catalytic approach to the synthesis of 3-acylindoles under Pd-Cu-cocatalyzed oxidative conditions is demonstrated. tert-Butyl hydroperoxide (TBHP) acts not only as the oxidant, but also as an oxygen source in the approach. The process allows quick and atom-economical assembly of 3-acylindoles from readily available starting materials and tolerates a broad range of functional groups.
Subject Area材料科学与物理化学
DOI10.1039/c2cc37805a
Funding Organizationthe National Science Foundation (NSF 21072080);National Basic Research Program of China (973 Program) 2010CB833203;“111” Program of MOE
Indexed BySCI
If6.718
Language英语
compositor第二作者单位
Citation statistics
Cited Times:57[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/18244
Collection固体润滑国家重点实验室(LSL)
Corresponding AuthorLiang YM(梁永民)
Affiliation1.Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
2.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Solid Lubricat, Lanzhou 730000, Peoples R China
Recommended Citation
GB/T 7714
Xia XF,Zhang, Lu-Lu,Song XR,et al. Palladium-copper-cocatalyzed intramolecular oxidative coupling: an efficient and atom-economical strategy for the synthesis of 3-acylindoles[J]. Chemical Communications,2013,49(14):1410-1412.
APA Xia XF.,Zhang, Lu-Lu.,Song XR.,Niu YN.,Liu XY.,...&梁永民.(2013).Palladium-copper-cocatalyzed intramolecular oxidative coupling: an efficient and atom-economical strategy for the synthesis of 3-acylindoles.Chemical Communications,49(14),1410-1412.
MLA Xia XF,et al."Palladium-copper-cocatalyzed intramolecular oxidative coupling: an efficient and atom-economical strategy for the synthesis of 3-acylindoles".Chemical Communications 49.14(2013):1410-1412.
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