Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/104207
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dc.contributor.authorFang, Xinqiangen
dc.contributor.authorChen, Xingkuanen
dc.contributor.authorLv, Huien
dc.contributor.authorChi, Robin Yongguien
dc.date.accessioned2014-05-26T03:17:38Zen
dc.date.accessioned2019-12-06T21:28:27Z-
dc.date.available2014-05-26T03:17:38Zen
dc.date.available2019-12-06T21:28:27Z-
dc.date.copyright2011en
dc.date.issued2011en
dc.identifier.citationFang, X., Chen, X., Lv, H., & Chi, Y. R. (2011). Enantioselective Stetter Reactions of Enals and Modified Chalcones Catalyzed by N-Heterocyclic Carbenes. Angewandte Chemie International Edition, 50(49), 11782–11785.en
dc.identifier.urihttps://hdl.handle.net/10356/104207-
dc.description.abstractNew trick for an old cat.: Triazolium-based N-heterocyclic carbenes (NHCs) catalyze the selective generation of acyl anion equivalents for the title reaction. The stereoelectronic properties of the enal-derived Breslow intermediates and the unique reactivity of the modified chalcones are crucial for the Stetter reactions to occur. EWG=electron- withdrawing group.en
dc.language.isoenen
dc.relation.ispartofseriesAngewandte chemie international editionen
dc.rights© 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.en
dc.subjectDRNTU::Science::Chemistry::Organic chemistryen
dc.titleEnantioselective Stetter reactions of enals and modified chalcones catalyzed by N-heterocyclic carbenesen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.1002/anie.201105812en
dc.identifier.rims173624en
item.grantfulltextnone-
item.fulltextNo Fulltext-
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