Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/104216
Title: Enantioselective sulfonation of enones with sulfonyl imines by cooperative N-heterocyclic-carbene/thiourea/tertiary-amine multicatalysis
Authors: Chi, Robin Yonggui
Jin, Zhichao
Xu, Jianfeng
Yang, Song
Song, Bao-An
Keywords: DRNTU::Science::Chemistry::Organic chemistry
Issue Date: 2013
Source: Jin, Z., Xu, J., Yang, S., Song, B.-A. & Chi, Y. R. (2013). Enantioselective Sulfonation of Enones with Sulfonyl Imines by Cooperative N-Heterocyclic-Carbene/Thiourea/Tertiary-Amine Multicatalysis. Angewandte Chemie International Edition, 52(47), 12354–12358.
Series/Report no.: Angewandte Chemie international edition
Abstract: Many hands make light work: In an organocatalytic asymmetric sulfonation of enones, the activation of a sulfonyl imine by an N-heterocyclic carbene (NHC) catalyst led to the release of a sulfinic anion, which underwent nucleophilic addition to the enone. The enantioselectivity of the process was controlled by a chiral thiourea/amine co-catalyst through anion recognition and hydrogen-bonding interactions. Tol=p-tolyl.
URI: https://hdl.handle.net/10356/104216
http://hdl.handle.net/10220/19451
ISSN: 1433-7851
DOI: 10.1002/anie.201305023
Rights: © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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