Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/95800
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dc.contributor.authorJiang, Yaojiaen
dc.contributor.authorChan, Wei Chuenen
dc.contributor.authorPark, Cheol-Minen
dc.date.accessioned2013-07-11T06:06:58Zen
dc.date.accessioned2019-12-06T19:21:48Z-
dc.date.available2013-07-11T06:06:58Zen
dc.date.available2019-12-06T19:21:48Z-
dc.date.copyright2012en
dc.date.issued2012en
dc.identifier.citationJiang, Y., Chan, W. C., & Park, C. M. (2012). Expedient Synthesis of Highly Substituted Pyrroles via Tandem Rearrangement of α-Diazo Oxime Ethers. Journal of the American Chemical Society, 134(9), 4104-4107.en
dc.identifier.urihttps://hdl.handle.net/10356/95800-
dc.identifier.urihttp://hdl.handle.net/10220/11202en
dc.description.abstractAn 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.en
dc.language.isoenen
dc.relation.ispartofseriesJournal of the American chemical societyen
dc.rights© 2012 American Chemical Society.en
dc.titleExpedient synthesis of highly substituted pyrroles via tandem rearrangement of α-diazo oxime ethersen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.1021/ja300552cen
item.grantfulltextnone-
item.fulltextNo Fulltext-
Appears in Collections:SPMS Journal Articles

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