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박철민

Park, Cheol-Min
Synthetic and Medicinal Chemistry Lab.
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dc.citation.endPage 4107 -
dc.citation.number 9 -
dc.citation.startPage 4104 -
dc.citation.title JOURNAL OF THE AMERICAN CHEMICAL SOCIETY -
dc.citation.volume 134 -
dc.contributor.author Jiang, Yaojia -
dc.contributor.author Chan, Wei Chuen -
dc.contributor.author Park, Cheol-Min -
dc.date.accessioned 2023-12-22T05:16:24Z -
dc.date.available 2023-12-22T05:16:24Z -
dc.date.created 2014-11-10 -
dc.date.issued 2012-03 -
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. -
dc.identifier.bibliographicCitation JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.134, no.9, pp.4104 - 4107 -
dc.identifier.doi 10.1021/ja300552c -
dc.identifier.issn 0002-7863 -
dc.identifier.scopusid 2-s2.0-84863229529 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/8537 -
dc.identifier.url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84863229529 -
dc.identifier.wosid 000301550800045 -
dc.language 영어 -
dc.publisher AMER CHEMICAL SOC -
dc.title Expedient Synthesis of Highly Substituted Pyrroles via Tandem Rearrangement of alpha-Diazo Oxime Ethers -
dc.type Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus SPONGE DYSIDEA-FRAGILIS -
dc.subject.keywordPlus DIELS-ALDER REACTIONS -
dc.subject.keywordPlus WOLFF REARRANGEMENT -
dc.subject.keywordPlus CYCLOADDITION REACTIONS -
dc.subject.keywordPlus RING EXPANSION -
dc.subject.keywordPlus 2H-AZIRINES -
dc.subject.keywordPlus MULTICOMPONENT -
dc.subject.keywordPlus CHEMISTRY -
dc.subject.keywordPlus ISOXAZOLES -
dc.subject.keywordPlus ALKALOIDS -

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