LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
P(O)R-2-Directed Enantioselective C-H Olefination toward Chiral Atropoisomeric Phosphine-Olefin Compounds
DepartmentOSSO国家重点实验室
Li, Shi-Xia1; Ma YN(马艳娜)1; Yang SD(杨尚东)1,2; Yang SD(杨尚东)
2017
Source PublicationOrganic Letters
ISSN1523-7060
Volume19Issue:7Pages:1842-1845
Abstract

An effective synthesis of chiral atropoisomeric biaryl phosphine–olefin compounds via palladium-catalyzed enantioselective C–H olefination has been developed for the first time. The reactions are operationally simple, tolerate wide functional groups, and have a good ee value. Notably, P(O)R2 not only acts as the directing group to direct C–H activation in order to make a useful ligand but also serves to facilitate composition of the product in a useful manner in this transformation.

Subject Area物理化学与绿色催化
DOI10.1021/acs.orglett.7b00608
Funding Organizationthe NSFC (Nos. 21472076;21532001);PCSIRT (IRT_15R28;lzujbky-2016-ct02)
Indexed BySCI
Language英语
compositor第二作者单位
Citation statistics
Cited Times:86[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/21789
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, Shi-Xia,Ma YN,Yang SD,et al. P(O)R-2-Directed Enantioselective C-H Olefination toward Chiral Atropoisomeric Phosphine-Olefin Compounds[J]. Organic Letters,2017,19(7):1842-1845.
APA Li, Shi-Xia,Ma YN,Yang SD,&杨尚东.(2017).P(O)R-2-Directed Enantioselective C-H Olefination toward Chiral Atropoisomeric Phosphine-Olefin Compounds.Organic Letters,19(7),1842-1845.
MLA Li, Shi-Xia,et al."P(O)R-2-Directed Enantioselective C-H Olefination toward Chiral Atropoisomeric Phosphine-Olefin Compounds".Organic Letters 19.7(2017):1842-1845.
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