Diastereo- and enantioselective synthesis of 4- and 3,4-substituted 2-acetoxy-butyrolactones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. A Convenient Synthesis of γ-Alkyl-α-hydroxy-γ-lactones as a Food Intake-Control Substance
2. Synthesis of (S)- and (R)-3-Hydroxy-4-butanolide and (2S,4S)-, (2R,4S)-, (2S,4R)-, and (2R,4R)-2-Hydroxy-4-hydroxymethyl-4-butanolide and Their Satiety and Hunger Modulating Activities
3. Studies on the nactins: total synthesis of (.+-.)-tert-butyl 8-O-(tert-butyldimethylsilyl)nonactate
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1. Asymmetric synthesis of butyrolactones by aldol reactions;Studies in Natural Products Chemistry;2021
2. Total syntheses of both enantiomers of amphirionin 4: A chemoenzymatic based strategy for functionalized tetrahydrofurans;Tetrahedron;2017-04
3. A sialic acid aldolase from Peptoclostridium difficile NAP08 with 4-hydroxy-2-oxo-pentanoate aldolase activity;Enzyme and Microbial Technology;2016-10
4. A Concise Organocatalytic Synthesis of 3-Deoxy-2-ulosonic Acids throughCinchona-Alkaloid-Promoted Aldol Reactions of Pyruvate;European Journal of Organic Chemistry;2016-08-05
5. Enantioselective Total Synthesis of (+)-Amphirionin-4;Organic Letters;2016-04-26
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