Please use this identifier to cite or link to this item:
|Title:||Controlled β-protonation and [4+2] cycloaddition of enals and chalcones via N-heterocyclic carbene/acid catalysis : toward substrate independent reaction control||Authors:||Fu, Zhenqian
Chi, Robin Yonggui
|Issue Date:||2013||Source:||Fu, 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.||Series/Report no.:||Chemical communications||Abstract:||A 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.||URI:||https://hdl.handle.net/10356/97255
|DOI:||http://dx.doi.org/10.1039/c2cc36564b||Rights:||© 2013 The Royal Society of Chemistry.||Fulltext Permission:||none||Fulltext Availability:||No Fulltext|
|Appears in Collections:||SPMS Journal Articles|
Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.