Copper-Catalyzed Direct Synthesis of 1,2,4-Oxadiazoles from Amides and Organic Nitriles by Oxidative N-O Bond Formation
DC Field | Value | Language |
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dc.contributor.author | Kuram, Malleswara Rao | ko |
dc.contributor.author | Kim, Woo Gyum | ko |
dc.contributor.author | Myung, Kyungjae | ko |
dc.contributor.author | Hong, Sung You | ko |
dc.date.available | 2016-01-06T01:30:41Z | - |
dc.date.created | 2016-01-06 | ko |
dc.date.issued | 2016-01 | ko |
dc.identifier.citation | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, v.2016, no.3, pp.438 - 442 | ko |
dc.identifier.issn | 1434-193X | ko |
dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/18046 | - |
dc.description.abstract | Herein, we report the first Cu-catalyzed one-step method for the synthesis of 1,2,4-oxadiazoles from stable, less toxic, and readily available amides and organic nitriles by a rare oxidative N-O bond formation using O2 as sole oxidant. This method has a broad substrate scope and a good tolerance for diverse functional groups. Moreover, the synthetic utility of this method is highlighted by the synthesis of biologically active 3,5-disubstituted derivatives. | ko |
dc.description.statementofresponsibility | close | - |
dc.language | 영어 | ko |
dc.publisher | WILEY-V C H VERLAG GMBH | ko |
dc.title | Copper-Catalyzed Direct Synthesis of 1,2,4-Oxadiazoles from Amides and Organic Nitriles by Oxidative N-O Bond Formation | ko |
dc.type | ARTICLE | ko |
dc.identifier.scopusid | 2-s2.0-84957840719 | ko |
dc.identifier.wosid | 000368815700005 | ko |
dc.type.rims | ART | ko |
dc.description.wostc | 0 | * |
dc.description.scopustc | 0 | * |
dc.date.tcdate | 2016-02-11 | * |
dc.date.scptcdate | 2016-01-06 | * |
dc.identifier.doi | 10.1002/ejoc.201501502 | ko |
dc.identifier.url | http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201501502/abstract;jsessionid=6411E187B67E25916AA5444AA6C53AE4.f03t04 | ko |
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