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CuI/N,N-dimethylglycine-catalyzed synthesis of N-aryloxazolidinones from aryl bromides
Alternative Title碘化亚铜/N,N-二甲基甘氨酸催化的从芳基溴代物合成N-芳基噁唑啉酮
Li JJ(李姣姣); Zhang YH(张奕华); Jiang YW(蒋咏文); Ma DW(马大为)
Source PublicationTetrahedron Lett.
AbstractCuI/N,N-dimethylglycine catalyzed coupling of aryl bromides with substituted oxazolidinones took place at 120 degrees C in DMF, affording the corresponding N-arylation products with good to excellent yields. A number of functional groups, such as ketone, nitrile, nitro, methoxy, and hydroxyl were tolerated under these conditions, thereby allowing diversity synthesis of N-aryloxazolidinones. (C) 2012 Elsevier Ltd. All rights reserved.
Subject Area金属有机化学
Department中国药科大学; 中科院上海有机化学研究所
Indexed BySCI
WOS IDWOS:000306456300010
Citation statistics
Cited Times:14[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Corresponding AuthorZhang YH(张奕华); Ma DW(马大为)
Recommended Citation
GB/T 7714
Li JJ,Zhang YH,Jiang YW,et al. CuI/N,N-dimethylglycine-catalyzed synthesis of N-aryloxazolidinones from aryl bromides[J]. Tetrahedron Lett.,2012,53(31):3981-3983.
APA 李姣姣,张奕华,蒋咏文,&马大为.(2012).CuI/N,N-dimethylglycine-catalyzed synthesis of N-aryloxazolidinones from aryl bromides.Tetrahedron Lett.,53(31),3981-3983.
MLA 李姣姣,et al."CuI/N,N-dimethylglycine-catalyzed synthesis of N-aryloxazolidinones from aryl bromides".Tetrahedron Lett. 53.31(2012):3981-3983.
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