LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Regio- and Stereoselective Allylic C-H Arylation with Electron-Deficient Arenes by 1,1 '-Bi-2-naphthol-Palladium Cooperation
DepartmentOSSO国家重点实验室
Wang, Gang-Wei1; Zhou, An-Xi1; Li, Shi-Xia1; Yang SD(杨尚东)1,2; Yang SD(杨尚东)
2014
Source PublicationOrganic Letters
ISSN1523-7060
Volume16Issue:11Pages:3118-3121
Abstract

A palladium-catalyzed allylic C–H arylation reaction with electron-deficient arenes with high regio- and stereoselectivity is reported. This work represents the first successful use of 1,1′-bi-2-naphthol as the ancillary ligand in allylic C–H activation, which is the key factor for chemoselectivity. Furthermore, high selectivity allylic C–H acetoxylation and amination were also successfully achieved under the same catalytic system.

Subject Area物理化学与绿色催化
DOI10.1021/ol501247b
Funding Organizationthe NSFC (No. 21272100);Program for New Century Excellent Talents in University (NCET-11-0215;lzujbky-2013-k07)
Indexed BySCI
If6.364
Language英语
compositor第二作者单位
Citation statistics
Cited Times:44[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/21327
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, Peoples R China
Recommended Citation
GB/T 7714
Wang, Gang-Wei,Zhou, An-Xi,Li, Shi-Xia,et al. Regio- and Stereoselective Allylic C-H Arylation with Electron-Deficient Arenes by 1,1 '-Bi-2-naphthol-Palladium Cooperation[J]. Organic Letters,2014,16(11):3118-3121.
APA Wang, Gang-Wei,Zhou, An-Xi,Li, Shi-Xia,Yang SD,&杨尚东.(2014).Regio- and Stereoselective Allylic C-H Arylation with Electron-Deficient Arenes by 1,1 '-Bi-2-naphthol-Palladium Cooperation.Organic Letters,16(11),3118-3121.
MLA Wang, Gang-Wei,et al."Regio- and Stereoselective Allylic C-H Arylation with Electron-Deficient Arenes by 1,1 '-Bi-2-naphthol-Palladium Cooperation".Organic Letters 16.11(2014):3118-3121.
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