LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Palladium-Catalyzed sp(2) and sp(3) C-H Bond Activation and Addition to Isatin toward 3-Hydroxy-2-oxindoles
DepartmentOSSO国家重点实验室
Wang GW(王刚伟)1; Zhou AX(周安西)1; Wang JJ(王君姣)1; Hu RB(胡荣斌)1; Yang SD(杨尚东)1,2; Yang SD(杨尚东)
2013
Source PublicationOrganic Letters
ISSN1523-7060
Volume15Issue:20Pages:5270-5273
AbstractThe first Pd(II)-catalyzed C-H addition to isatins by direct sp2/sp3 C-H bond activation for the construction of 3-substituted-3-hydroxy-2-oxindoles is reported. The bidentate nitrogen ligands were found to promote this reaction. Specifically, the preliminary bioassay indicated that 3-(5-chlorobenzoxazole)-3-hydroxy-N-benzyl-2-oxindole (2w) is a new inhibitor of human kidney cancer and hepatocellular carcinoma cells. Moreover, this reaction system exhibits great functional group tolerance and requires no directing group, extra base, or additives.
Subject Area物理化学与绿色催化
DOI10.1021/oI402494e
Funding Organizationthe NSFC (Nos. 21072079;21272100);Program for New Century Excellent Talents in University (NCET-11-0215)
Indexed BySCI
If6.324
Language英语
compositor第二作者单位
Citation statistics
Cited Times:63[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/4953
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorYang SD(杨尚东)
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 Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
Recommended Citation
GB/T 7714
Wang GW,Zhou AX,Wang JJ,et al. Palladium-Catalyzed sp(2) and sp(3) C-H Bond Activation and Addition to Isatin toward 3-Hydroxy-2-oxindoles[J]. Organic Letters,2013,15(20):5270-5273.
APA Wang GW,Zhou AX,Wang JJ,Hu RB,Yang SD,&杨尚东.(2013).Palladium-Catalyzed sp(2) and sp(3) C-H Bond Activation and Addition to Isatin toward 3-Hydroxy-2-oxindoles.Organic Letters,15(20),5270-5273.
MLA Wang GW,et al."Palladium-Catalyzed sp(2) and sp(3) C-H Bond Activation and Addition to Isatin toward 3-Hydroxy-2-oxindoles".Organic Letters 15.20(2013):5270-5273.
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