Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/81750
DC Field | Value | Language |
---|---|---|
dc.contributor | Department of Applied Biology and Chemical Technology | - |
dc.creator | Liu, YP | - |
dc.creator | Lu, LX | - |
dc.creator | Zhou, HP | - |
dc.creator | Xu, FJ | - |
dc.creator | Ma, C | - |
dc.creator | Huang, ZJ | - |
dc.creator | Xu, JY | - |
dc.creator | Xu, ST | - |
dc.date.accessioned | 2020-02-10T12:28:58Z | - |
dc.date.available | 2020-02-10T12:28:58Z | - |
dc.identifier.uri | http://hdl.handle.net/10397/81750 | - |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.rights | This journal is © The Royal Society of Chemistry 2019 | en_US |
dc.rights | This article is licensed under a Creative Commons Attibution-NonCommercial 3.0 Unported Licence (https://creativecommons.org/licenses/by-nc/3.0/) | en_US |
dc.rights | The following publication Liu, Y. P., Lu, L. X., Zhou, H. P., Xu, F. J., Ma, C., Huang, Z. J., . . . Xu, S. T. (2019). Chemodivergent synthesis of n-(pyridin-2-yl)amides and 3-bromoimidazo[1,2-a]pyridines from alpha-bromoketones and 2-aminopyridines. RSC Advances, 9(59), 34671-34676 is available at https://dx.doi.org/10.1039/c9ra06724h | en_US |
dc.title | Chemodivergent synthesis of n-(pyridin-2-yl)amides and 3-bromoimidazo[1,2-a]pyridines from alpha-bromoketones and 2-aminopyridines | en_US |
dc.type | Journal/Magazine Article | en_US |
dc.identifier.spage | 34671 | - |
dc.identifier.epage | 34676 | - |
dc.identifier.volume | 9 | - |
dc.identifier.issue | 59 | - |
dc.identifier.doi | 10.1039/c9ra06724h | - |
dcterms.abstract | N-(Pyridin-2-yl)amides and 3-bromoimidazo[1,2-a]pyridines were synthesized respectively from alpha-bromoketones and 2-aminopyridine under different reaction conditions. N-(Pyridin-2-yl)amides were formed in toluene via C-C bond cleavage promoted by I-2 and TBHP and the reaction conditions were mild and metal-free. Whereas 3-bromoimidazopyridines were obtained in ethyl acetate via one-pot tandem cyclization/bromination when only TBHP was added, the cyclization to form imidazopyridines was promoted by the further bromination, no base was needed, and the versatile 3-bromoimidazopyridines could be further transferred to other skeletons. | - |
dcterms.accessRights | open access | en_US |
dcterms.bibliographicCitation | RSC advances, 2019, v. 9, no. 59, p. 34671-34676 | - |
dcterms.isPartOf | RSC advances | - |
dcterms.issued | 2019 | - |
dc.identifier.isi | WOS:000494684600065 | - |
dc.identifier.eissn | 2046-2069 | - |
dc.description.validate | 202002 bcrc | - |
dc.description.oa | Version of Record | en_US |
dc.identifier.FolderNumber | OA_Scopus/WOS | en_US |
dc.description.pubStatus | Published | en_US |
Appears in Collections: | Journal/Magazine Article |
Files in This Item:
File | Description | Size | Format | |
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Liu_Chemodivergent_Synthesis_N-(pyridin-2-yl)amides.pdf | 891.83 kB | Adobe PDF | View/Open |
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