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Park, Cheol-Min
Synthetic & Medicinal Chemistry Lab
Research Interests
  • Organic synthesis, medicinal chemistry, chemical biology

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Carbenoid-mediated N-O bond insertion and its application in the synthesis of pyridines

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dc.contributor.author Qi, Xinxin ko
dc.contributor.author Dai, Lu ko
dc.contributor.author Park, Cheol-Min ko
dc.date.available 2014-11-11T00:12:15Z -
dc.date.created 2014-11-10 ko
dc.date.issued 2012-10 -
dc.identifier.citation CHEMICAL COMMUNICATIONS, v.48, no.91, pp.11244 - 11246 ko
dc.identifier.issn 1359-7345 ko
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/8486 -
dc.identifier.uri http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84868028814 ko
dc.description.abstract Highly efficient synthesis of 3-hydroxypyridines has been developed based on carbenoid-mediated N-O bond insertion. Treatment of δ-diazo oxime ethers with dirhodium complex Rh2(tfacam)4 rapidly provides a variety of pyridines in 5-10 minutes in good to excellent yields. ko
dc.description.statementofresponsibility close -
dc.language ENG ko
dc.publisher ROYAL SOC CHEMISTRY ko
dc.subject DE-NOVO SYNTHESIS ko
dc.subject DIELS-ALDER REACTION ko
dc.subject ONE-POT SYNTHESIS ko
dc.subject DERIVATIVES ko
dc.subject CYCLOADDITION ko
dc.subject ALKYNES ko
dc.subject 1,2,4-TRIAZINES ko
dc.subject ISOQUINOLINES ko
dc.subject CYCLIZATION ko
dc.subject ACETYLENES ko
dc.title Carbenoid-mediated N-O bond insertion and its application in the synthesis of pyridines ko
dc.type ARTICLE ko
dc.identifier.scopusid 2-s2.0-84868028814 ko
dc.identifier.wosid 000310068800024 ko
dc.type.rims ART ko
dc.description.wostc 5 *
dc.description.scopustc 3 *
dc.date.tcdate 2015-05-06 *
dc.date.scptcdate 2014-11-10 *
dc.identifier.doi 10.1039/c2cc36009h ko
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