Carbohydrates as chiral auxiliaries in enantioselective synthesis of four stereoisomers of optically active α,γ-substituted γ-butyrolactones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Synthesis of 6-(Bromoacetyl)amino-2,3-dimorpholinoquinoxaline and Application to a New Fluorescence Derivatization Reagent of Fatty Acids for the High-Performance Liquid Chromatographic Analysis
2. Synthesis of (+)- and (−)-Phaseolinic Acid by Combination of Enzymatic Hydrolysis and Chemical Transformations with Revision of the Absolute Configuration of the Natural Product
3. A Facile Synthesis of Chiral γ-Butyrolactones in Extremely High Enantioselectivity Mediated by Samarium(II) Iodide
4. Development of a New Reaction System for the Synthesis of Highly Optically Active α,γ-Substituted γ-Butyrolactones
5. A Highly Efficient Asymmetric Synthesis of Optically Active α,γ-Substituted γ-Butyrolactones Using a Chiral Auxiliary Derived from Isosorbide
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2. Selectivity controlled by ligand tuning in the palladium-catalysed cyclocarbonylation: Synthesis of new γ and δ lactones from a natural sesquiterpene;Journal of Molecular Catalysis A: Chemical;2015-05
3. Electroreductive Coupling of Optically Active α,β-Unsaturated Carbonyl Compounds with Diaryl Ketones: Asymmetric Synthesis of 4,5,5-Trisubstituted γ-Butyrolactones;Organic Letters;2014-06-05
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