LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Alcohol assisted C-C bond breaking: copper-catalyzed deacetylative alpha-arylation of beta-keto esters and amides
DepartmentOSSO国家重点实验室
Ke J(柯杰)1; He C(何川)1; Liu HY(柳慧颖)1; Xu H(许焕)1; Lei AW(雷爱文)1,2; Lei AW(雷爱文)
2013
Source PublicationChemical Communications
ISSN1359-7345
Volume49Issue:60Pages:6767-6769
AbstractA method of alcohol-assisted copper-catalyzed highly selective deacetylative α-arylation of β-keto esters and amides has been demonstrated, which illustrated an efficient example of achieving α-aryl esters and amides. From the synthetic point of view, this arylation protocol is general and practical, representing a simple way to produce α-arylated carbonyl compounds from basic starting materials at low cost.
Subject Area物理化学与绿色催化
DOI10.1039/c3cc43279c
Funding Organizationthe 973 Program (2012CB725302);the National Natural Science Foundation of China (21025206;21272180);the Program for Changjiang Scholars and Innovative Research Team in University (IRT1030)
Indexed BySCI
If6.718
Language英语
compositor第二作者单位
Citation statistics
Cited Times:22[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/4856
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorLei AW(雷爱文)
Affiliation1.Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Hubei, Peoples R China
2.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
Recommended Citation
GB/T 7714
Ke J,He C,Liu HY,et al. Alcohol assisted C-C bond breaking: copper-catalyzed deacetylative alpha-arylation of beta-keto esters and amides[J]. Chemical Communications,2013,49(60):6767-6769.
APA Ke J,He C,Liu HY,Xu H,Lei AW,&雷爱文.(2013).Alcohol assisted C-C bond breaking: copper-catalyzed deacetylative alpha-arylation of beta-keto esters and amides.Chemical Communications,49(60),6767-6769.
MLA Ke J,et al."Alcohol assisted C-C bond breaking: copper-catalyzed deacetylative alpha-arylation of beta-keto esters and amides".Chemical Communications 49.60(2013):6767-6769.
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