Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/104209
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dc.contributor.authorChen, Xingkuanen
dc.contributor.authorYang, Songen
dc.contributor.authorSong, Bao-Anen
dc.contributor.authorChi, Robin Yongguien
dc.date.accessioned2014-05-26T02:29:00Zen
dc.date.accessioned2019-12-06T21:28:28Z-
dc.date.available2014-05-26T02:29:00Zen
dc.date.available2019-12-06T21:28:28Z-
dc.date.copyright2013en
dc.date.issued2013en
dc.identifier.citationChen, X., Yang, S., Song, B.-A., & Chi, Y. R. (2013). Functionalization of Benzylic C(sp3)H Bonds of Heteroaryl Aldehydes through N-Heterocyclic Carbene Organocatalysis. Angewandte Chemie International Edition, 52(42), 11134–11137.en
dc.identifier.issn1433-7851en
dc.identifier.urihttps://hdl.handle.net/10356/104209-
dc.description.abstractAryl aldehyde activation: Oxidative activation of 2-methylindole-3-carboxaldehyde (I) through N-heterocyclic carbene (NHC) organocatalysis generates heterocyclic ortho-quinodimethane (II) as a key intermediate. This intermediate then undergoes formal [4+2] cycloaddition with trifluoromethyl ketones or isatins to form polycyclic lactones containing a quaternary carbon center.en
dc.language.isoenen
dc.relation.ispartofseriesAngewandte Chemie international editionen
dc.rights© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.en
dc.subjectDRNTU::Science::Chemistry::Organic chemistryen
dc.titleFunctionalization of benzylic C(sp3)H bonds of heteroaryl aldehydes through N-heterocyclic carbene organocatalysisen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.1002/anie.201305861en
dc.identifier.rims179770en
item.fulltextNo Fulltext-
item.grantfulltextnone-
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