Controlled β-protonation and [4+2] cycloaddition of enals and chalcones via N-heterocyclic carbene/acid catalysis : toward substrate independent reaction control

Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/97255

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 Sun, Hui Chen, Shaojin Tiwari, Bhoopendra Li, Guohui 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 http://hdl.handle.net/10220/10471
DOI:	10.1039/c2cc36564b
Schools:	School of Physical and Mathematical Sciences
Rights:	© 2013 The Royal Society of Chemistry.
Fulltext Permission:	none
Fulltext Availability:	No Fulltext
Appears in Collections:	SPMS Journal Articles

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