Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/96081
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dc.contributor.authorToh, Kah Kahen
dc.contributor.authorSanjaya, Stephenen
dc.contributor.authorSahnoun, Sophianen
dc.contributor.authorChong, Sin Yeeen
dc.contributor.authorChiba, Shunsukeen
dc.date.accessioned2013-06-25T03:46:18Zen
dc.date.accessioned2019-12-06T19:25:19Z-
dc.date.available2013-06-25T03:46:18Zen
dc.date.available2019-12-06T19:25:19Z-
dc.date.copyright2012en
dc.date.issued2012en
dc.identifier.citationToh, K. K., Sanjaya, S., Sahnoun, S., Chong, S. Y., & Chiba, S. (2012). Copper-Catalyzed Aerobic Intramolecular Carbo- and Amino-Oxygenation of Alkynes for Synthesis of Azaheterocycles. Organic Letters, 14(9), 2290-2292.en
dc.identifier.issn1523-7060en
dc.identifier.urihttps://hdl.handle.net/10356/96081-
dc.identifier.urihttp://hdl.handle.net/10220/10603en
dc.description.abstractA synthetic method of highly substituted quinolines has been developed from N-(2-alkynylaryl)enamine carboxylates under Cu-catalyzed aerobic conditions via intramolecular carbo-oxygenation of alkynes. This strategy was further applied for N-alkynylamidines for amino-oxygenation of alkynes, leading to imidazole and quinazoline derivatives.en
dc.language.isoenen
dc.relation.ispartofseriesOrganic lettersen
dc.rights© 2012 American Chemical Society.en
dc.titleCopper-catalyzed aerobic intramolecular carbo- and amino-oxygenation of alkynes for synthesis of azaheterocyclesen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doihttp://dx.doi.org/10.1021/ol3007106en
item.grantfulltextnone-
item.fulltextNo Fulltext-
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