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
Rights: © 2013 The Royal Society of Chemistry.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.