LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Palladium-Catalyzed Difunctionalization of Enol Ethers to Amino Acetals with Aminals and Alcohols
DepartmentOSSO国家重点实验室
Xie YJ(谢银君); Hu JH(胡建华); Jie P(解攀); Qian B(钱波); Huang HM(黄汉民); Huang HM(黄汉民)
2013
Source PublicationJournal of the American Chemical Society
ISSN0002-7863
Volume135Issue:49Pages:18327-18330
AbstractA new strategy was developed for intercepting the palladium alkyl species generated in Heck reaction via nucleophilic addition prior to the step of migratory insertion, which leads to a new palladium-catalyzed difunctionalization of enol ethers with aminals and alcohols to afford amino acetals. Mechanistic studies suggested that the cationic cyclometalated Pd(II) complex generated by the oxidative addition of aminal to a Pd(0) species was crucial for this unusual transformation.
Subject Area物理化学与绿色催化
DOI10.1021/ja410611b
Funding Organizationthe Chinese Academy of Sciences;the National Natural Science Foundation of China (21222203;21172226;21133011)
Indexed BySCI
If11.444
Language英语
Funding Project有机功能材料研究组
compositor第一作者单位
Citation statistics
Cited Times:97[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/4781
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorHuang HM(黄汉民)
AffiliationChinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
Recommended Citation
GB/T 7714
Xie YJ,Hu JH,Jie P,et al. Palladium-Catalyzed Difunctionalization of Enol Ethers to Amino Acetals with Aminals and Alcohols[J]. Journal of the American Chemical Society,2013,135(49):18327-18330.
APA Xie YJ,Hu JH,Jie P,Qian B,Huang HM,&黄汉民.(2013).Palladium-Catalyzed Difunctionalization of Enol Ethers to Amino Acetals with Aminals and Alcohols.Journal of the American Chemical Society,135(49),18327-18330.
MLA Xie YJ,et al."Palladium-Catalyzed Difunctionalization of Enol Ethers to Amino Acetals with Aminals and Alcohols".Journal of the American Chemical Society 135.49(2013):18327-18330.
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