Chiron approach towards optically pure γ-valerolactone from alanine
Author:
Affiliation:
1. Technology Development Centre, Custom Pharmaceutical Services, Dr. Reddy’s Laboratories Ltd, Hyderabad, India;
2. Department of Organic Chemistry and FDW, Andhra University, Visakhapatnam, India
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2018.1491993
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1. Selective Serotonin Reuptake Inhibitors (SSRIs): Therapeutic Drug Monitoring and Pharmacological Interactions
2. Direct asymmetric reduction of levulinic acid to gamma-valerolactone: synthesis of a chiral platform molecule
3. Phenyl-substituted prostaglandins: potent and selective antiglaucoma agents
4. Selective Reductions. 59. Effective Intramolecular Asymmetric Reductions of α-, β-, and γ-Keto Acids with Diisopinocampheylborane and Intermolecular Asymmetric Reductions of the Corresponding Esters with B-Chlorodiisopinocampheylborane
5. A convenient route to chiral γ-lactones via asymmetric hydrogenation of γ-ketoesters using the RuCl3–BINAP–HCl catalytic system
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1. Stereoselective Synthesis of γ‐(Acyloxy)carboxylic Acids and γ‐Lactones Featuring the Switch of Stereopreference of Candida antarctica Lipase B in Sodium γ‐Hydroxycarboxylate Homologues;European Journal of Organic Chemistry;2022-12-28
2. Formal synthesis of Cladospolide C & epi-Cladospolide C using R-(+)-γ-valerolactone as a chiral synthon;Tetrahedron;2019-05
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