Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/97255
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dc.contributor.authorFu, Zhenqianen
dc.contributor.authorSun, Huien
dc.contributor.authorChen, Shaojinen
dc.contributor.authorTiwari, Bhoopendraen
dc.contributor.authorLi, Guohuien
dc.contributor.authorChi, Robin Yongguien
dc.date.accessioned2013-06-17T08:16:10Zen
dc.date.accessioned2019-12-06T19:40:37Z-
dc.date.available2013-06-17T08:16:10Zen
dc.date.available2019-12-06T19:40:37Z-
dc.date.copyright2013en
dc.date.issued2013en
dc.identifier.citationFu, Z., Sun, H., Chen, S., Tiwari, B., Li, G., & Chi, Y. R. (2013). Controlled β-protonation and [4+2] cycloaddition of enals and chalcones via N-heterocyclic carbene/acid catalysis: toward substrate independent reaction control. Chemical Communications, 49, 261-263.en
dc.identifier.urihttps://hdl.handle.net/10356/97255-
dc.description.abstractA substrate-independent selective generation of enolates over homoenolate equivalents in NHC-catalyzed reactions of enals and chalcones is disclosed. Acid co-catalysts play vital roles in control of the reaction pathways, allowing for individual access to diverse products from identical substrates.en
dc.language.isoenen
dc.relation.ispartofseriesChemical communicationsen
dc.rights© 2013 The Royal Society of Chemistry.en
dc.titleControlled β-protonation and [4+2] cycloaddition of enals and chalcones via N-heterocyclic carbene/acid catalysis : toward substrate independent reaction controlen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.1039/c2cc36564ben
dc.identifier.rims173461en
item.grantfulltextnone-
item.fulltextNo Fulltext-
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