ICCAS OpenIR
Nickel-Catalyzed Amination of Aryl Phosphates through Cleaving Aryl C-O Bonds
Huang, Jin-Hua; Yang, Lian-Ming1
2011-07-15
Source PublicationORGANIC LETTERS
ISSN1523-7060
Volume13Issue:14Pages:3750-3753
AbstractThe amination of triaryl phosphates was achieved using a Ni(II)-(sigma-Aryl) complex/NHC catalyst system In dioxane at 110 degrees C in the presence of NaH as base. Electron-neutral, -rich, and -deficient triaryl phosphates were coupled with a wider range of amine partners including cyclic and acyclic secondary amines, aliphatic primary amines, and anilines in good to excellent yields.
DOI10.1021/ol201437g
Indexed BySCI ; CCR
Language英语
WOS IDWOS:000292479300051
PublisherAMER CHEMICAL SOC
Citation statistics
Cited Times:51[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/73766
Collection中国科学院化学研究所
Corresponding AuthorYang, Lian-Ming
Affiliation1.Chinese Acad Sci, Beijing Natl Lab Mol Sci BNLMS, Inst Chem, New Mat Lab, Beijing 100190, Peoples R China
2.Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
Recommended Citation
GB/T 7714
Huang, Jin-Hua,Yang, Lian-Ming. Nickel-Catalyzed Amination of Aryl Phosphates through Cleaving Aryl C-O Bonds[J]. ORGANIC LETTERS,2011,13(14):3750-3753.
APA Huang, Jin-Hua,&Yang, Lian-Ming.(2011).Nickel-Catalyzed Amination of Aryl Phosphates through Cleaving Aryl C-O Bonds.ORGANIC LETTERS,13(14),3750-3753.
MLA Huang, Jin-Hua,et al."Nickel-Catalyzed Amination of Aryl Phosphates through Cleaving Aryl C-O Bonds".ORGANIC LETTERS 13.14(2011):3750-3753.
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