From the Feist-Bénary reaction to organocatalytic domino Michael-alkylation reactions: Asymmetric synthesis of 3(2H)-furanones

Please use this identifier to cite or link to this item: https://doi.org/10.1002/chem.201102796

Title:	From the Feist-Bénary reaction to organocatalytic domino Michael-alkylation reactions: Asymmetric synthesis of 3(2H)-furanones
Authors:	Dou, X. Han, X. Lu, Y.
Keywords:	asymmetric synthesis domino reactions Feist-Bénary reaction furanones organocatalysis
Issue Date:	2-Jan-2012
Citation:	Dou, X., Han, X., Lu, Y. (2012-01-02). From the Feist-Bénary reaction to organocatalytic domino Michael-alkylation reactions: Asymmetric synthesis of 3(2H)-furanones. Chemistry - A European Journal 18 (1) : 85-89. ScholarBank@NUS Repository. https://doi.org/10.1002/chem.201102796
Abstract:	It all adds up! A modified Feist-Bénary reaction employing a domino Michael-alkylation sequence was designed for the enantioselective synthesis of 3(2H)-furanones. L-Threonine-derived tertiary amine/thiourea catalysts were prepared for the first time; such catalysts promoted the designed domino Michael-alkylation reactions in a highly enantioselective manner (see scheme). Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Source Title:	Chemistry - A European Journal
URI:	http://scholarbank.nus.edu.sg/handle/10635/76224
ISSN:	09476539
DOI:	10.1002/chem.201102796
Appears in Collections:	Staff Publications

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