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박철민

Park, Cheol-Min
Synthetic and Medicinal Chemistry Lab.
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Expedient Synthesis of Highly Substituted Pyrroles via Tandem Rearrangement of alpha-Diazo Oxime Ethers

Author(s)
Jiang, YaojiaChan, Wei ChuenPark, Cheol-Min
Issued Date
2012-03
DOI
10.1021/ja300552c
URI
https://scholarworks.unist.ac.kr/handle/201301/8537
Fulltext
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84863229529
Citation
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.134, no.9, pp.4104 - 4107
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.
Publisher
AMER CHEMICAL SOC
ISSN
0002-7863
Keyword
SPONGE DYSIDEA-FRAGILISDIELS-ALDER REACTIONSWOLFF REARRANGEMENTCYCLOADDITION REACTIONSRING EXPANSION2H-AZIRINESMULTICOMPONENTCHEMISTRYISOXAZOLESALKALOIDS

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