LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Direct Functionalization of Tetrahydrofuran and 1,4-Dioxane: Nickel-Catalyzed Oxidative C(sp(3))-H Arylation
DepartmentOSSO国家重点实验室
Liu D(刘冬)1; Liu C(刘超)1; Li, Heng1; Lei AW(雷爱文)1,2; Lei AW(雷爱文)
2013
Source PublicationAngewandte Chemie International Edition
ISSN1433-7851
Volume52Issue:16Pages:4453-4456
KeywordC-h Functionalization Nickel Oxidative Coupling Radical Reactions Tetrahydrofuran
Subject Area物理化学与绿色催化
DOI10.1002/anie.201300459
Funding Organizationthe 973 Program (2012CB725302);the National Natural Science Foundation of China (21025206;21272180);the China Postdoctoral Science Foundation funded project (2012M521458);the Program for Changjiang Scholars and Innovative Research Team in University (IRT1030)
Indexed BySCI
If11.336
Language英语
compositor第二作者单位
Citation statistics
Cited Times:263[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/4852
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, 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
Liu D,Liu C,Li, Heng,et al. Direct Functionalization of Tetrahydrofuran and 1,4-Dioxane: Nickel-Catalyzed Oxidative C(sp(3))-H Arylation[J]. Angewandte Chemie International Edition,2013,52(16):4453-4456.
APA Liu D,Liu C,Li, Heng,Lei AW,&雷爱文.(2013).Direct Functionalization of Tetrahydrofuran and 1,4-Dioxane: Nickel-Catalyzed Oxidative C(sp(3))-H Arylation.Angewandte Chemie International Edition,52(16),4453-4456.
MLA Liu D,et al."Direct Functionalization of Tetrahydrofuran and 1,4-Dioxane: Nickel-Catalyzed Oxidative C(sp(3))-H Arylation".Angewandte Chemie International Edition 52.16(2013):4453-4456.
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