LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Sc(OTf)(3)-Catalyzed Dehydrogenative Cyclization for Synthesis of N-Methylacridones
DepartmentOSSO国家重点实验室
Li XA(李喜安)1; Wang HL(王红利)1; Yang SD(杨尚东)1,2; Yang SD(杨尚东)
2013
Source PublicationOrganic Letters
ISSN1523-7060
Volume15Issue:8Pages:1794-1797
AbstractA novel method has been developed for the synthesis of substituted N-methylacridones from 2-(N-methyl-N-phenylamino)benzaldehydes via dehydrogenative cyclization. This transformation involves two primary processes: the aldehyde first coordinates with Sc(OTf)3 and induces the aromatic electrophilic substitution (SEAr) reaction to formthe active intermediate N-methyl-acridin-9-ol,which is then quickly oxidized in situ to afford the acridones. Furthermore, the procedure involved is both environmental friendly and atom efficient; H2O is the only byproduct in this reaction.
Subject Area物理化学与绿色催化
DOI10.1021/ol400371h
Funding Organizationthe NSFC (Nos. 21072079;21272100);Program for Changjiang Scholars and Innovative Research Team in University (PCSIRT: IRT1138)
Indexed BySCI
If6.324
Language英语
compositor第二作者单位
Citation statistics
Cited Times:38[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/4950
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
Li XA,Wang HL,Yang SD,et al. Sc(OTf)(3)-Catalyzed Dehydrogenative Cyclization for Synthesis of N-Methylacridones[J]. Organic Letters,2013,15(8):1794-1797.
APA Li XA,Wang HL,Yang SD,&杨尚东.(2013).Sc(OTf)(3)-Catalyzed Dehydrogenative Cyclization for Synthesis of N-Methylacridones.Organic Letters,15(8),1794-1797.
MLA Li XA,et al."Sc(OTf)(3)-Catalyzed Dehydrogenative Cyclization for Synthesis of N-Methylacridones".Organic Letters 15.8(2013):1794-1797.
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