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Myung, Kyungjae
Center for Genomic Integrity
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Copper-Catalyzed Direct Synthesis of 1,2,4-Oxadiazoles from Amides and Organic Nitriles by Oxidative N-O Bond Formation

Author(s)
Kuram, Malleswara RaoKim, Woo GyumMyung, KyungjaeHong, Sung You
Issued Date
2016-01
DOI
10.1002/ejoc.201501502
URI
https://scholarworks.unist.ac.kr/handle/201301/18046
Fulltext
http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201501502/abstract;jsessionid=6411E187B67E25916AA5444AA6C53AE4.f03t04
Citation
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, v.2016, no.3, pp.438 - 442
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.
Publisher
WILEY-V C H VERLAG GMBH
ISSN
1434-193X
Keyword (Author)
CopperHeterocycles1, 2, 4-OxadiazolesHomogeneous catalysisCyclization
Keyword
ONE-POT SYNTHESISMEDIATED 1,3-DIPOLAR CYCLOADDITIONEFFICIENT SYNTHESISAMIDOXIMESDISCOVERYDESIGNFUNCTIONALIZATION1,2,4-TRIAZOLES1,2,3-TRIAZOLESCYCLIZATION

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