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• W2046539781 endingPage "89" @default.
• W2046539781 startingPage "85" @default.
• W2046539781 abstract "It all adds up! A modified Feist–Bénary reaction employing a domino Michael–alkylation sequence was designed for the enantioselective synthesis of 3(2 H)-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). Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
• W2046539781 created "2016-06-24" @default.
• W2046539781 creator A5006564007 @default.
• W2046539781 creator A5055068824 @default.
• W2046539781 creator A5066554626 @default.
• W2046539781 date "2011-12-12" @default.
• W2046539781 modified "2023-10-18" @default.
• W2046539781 title "From the Feist-Bénary Reaction to Organocatalytic Domino Michael-Alkylation Reactions: Asymmetric Synthesis of 3(2 H)-Furanones" @default.
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