LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Pd-carbene catalyzed carbonylation reactions of aryl iodides
Department羰基合成与选择氧化国家重点实验室
Xue LQ(薛立芹); Shi LJ(石利军); Han Y(韩源); Xia CG(夏春谷); Han Vinh Huynh; Li FW(李福伟)
2011
Source PublicationDalton Trans.
ISSN1477-9226
Volume40Issue:29Pages:7632-7638
AbstractA series of carbene complexes [PdBr2(iPr2-bimy)L] (C2–C13) with different types of co-ligands (L) have been tested for their catalytic activities in the carbonylative annulation of 2-iodophenol with phenylacetylene in DMF to afford the respective flavone 2a. Complex C12 with an N-phenylimidazole co-ligand showed the best activity and also afforded high yields when the substrate scope was extended to other aryl or pyridyl acetylenes. In addition, catalyst C12 was also efficient in the carbonylative annulation of 2-iodoaniline with acid chlorides giving the desirable 2-substituted 4H-3,1-benzoxazin- 4-ones (4) in good yields. Additionally, this Pd–NHC complex also proved to be a very efficient catalyst for the hydroxycarbonylation of iodobenzene derivatives at low catalyst loading and under low CO pressure. These results demonstrate the versatility and efficiency of this phosphine-free Pd(II)–NHC complex in different types of carbonylations of aryl iodides under mild conditions.
Subject Area均相催化
Funding Organizationthe National Natural Science Foundation of China (21002106 and 20625308) and the Chinese Academy of Science
Indexed BySCI
Language英语
Funding Project均相催化研究组
Citation statistics
Cited Times:69[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/329
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorLi FW(李福伟)
Recommended Citation
GB/T 7714
Xue LQ,Shi LJ,Han Y,et al. Pd-carbene catalyzed carbonylation reactions of aryl iodides[J]. Dalton Trans.,2011,40(29):7632-7638.
APA 薛立芹,石利军,韩源,夏春谷,Han Vinh Huynh,&李福伟.(2011).Pd-carbene catalyzed carbonylation reactions of aryl iodides.Dalton Trans.,40(29),7632-7638.
MLA 薛立芹,et al."Pd-carbene catalyzed carbonylation reactions of aryl iodides".Dalton Trans. 40.29(2011):7632-7638.
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