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

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Expedient Synthesis of Highly Substituted Pyrroles via Tandem Rearrangement of alpha-Diazo Oxime Ethers

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dc.contributor.author Jiang, Yaojia ko
dc.contributor.author Chan, Wei Chuen ko
dc.contributor.author Park, Cheol-Min ko
dc.date.available 2014-11-11T00:15:51Z -
dc.date.created 2014-11-10 ko
dc.date.issued 2012-03 -
dc.identifier.citation JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.134, no.9, pp.4104 - 4107 ko
dc.identifier.issn 0002-7863 ko
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/8537 -
dc.identifier.uri http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84863229529 ko
dc.description.abstract An efficient rhodium-catalyzed synthesis of 2H-azirines and pyrroles has been developed. Novel rearrangement of α-oximino ketenes derived from α-diazo oxime ethers provides 2H-azirines bearing quaternary centers and allows for subsequent rearrangement to highly substituted pyrroles in excellent yields. ko
dc.description.statementofresponsibility close -
dc.language ENG ko
dc.publisher AMER CHEMICAL SOC ko
dc.subject 2H-Azirines ko
dc.subject Oxime ethers ko
dc.subject Quaternary centers ko
dc.subject Rhodium-catalyzed synthesis ko
dc.title Expedient Synthesis of Highly Substituted Pyrroles via Tandem Rearrangement of alpha-Diazo Oxime Ethers ko
dc.type ARTICLE ko
dc.identifier.scopusid 2-s2.0-84863229529 ko
dc.identifier.wosid 000301550800045 ko
dc.type.rims ART ko
dc.description.wostc 49 *
dc.description.scopustc 37 *
dc.date.tcdate 2015-05-06 *
dc.date.scptcdate 2014-11-10 *
dc.identifier.doi 10.1021/ja300552c ko
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