A quick and regioselective access of spirooxindole‐oxazoline by reaction of isatin and isocyanoacetate “on water”
Author:
Affiliation:
1. Department of Medicinal ChemistryNational Institute of Pharmaceutical Education and Research (NIPER), Raebareli, Transit Campus Lucknow Uttar Pradesh India
Publisher
Wiley
Subject
Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.3953
Reference40 articles.
1. Enantioselective gem-Chlorofluorination of Active Methylene Compounds Using a Chiral Spiro Oxazoline Ligand
2. Highly Enantioselective Chlorination of β-Keto Esters and Subsequent SN2 Displacement of Tertiary Chlorides: A Flexible Method for the Construction of Quaternary Stereogenic Centers
3. Catalytic Stereoselective Synthesis of Diverse Oxindoles and Spirooxindoles from Isatins
4. Inhibitors of β-Site Amyloid Precursor Protein Cleaving Enzyme (BACE1): Identification of (S)-7-(2-Fluoropyridin-3-yl)-3-((3-methyloxetan-3-yl)ethynyl)-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-oxazol]-2′-amine (AMG-8718)
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1. Molecular Rearrangement of 2‐Substituted Indazolones: Unorthodox Access to 2‐Carboxylate‐2,3‐dihydroquinazolin‐4‐(1 H )‐one Scaffold;Asian Journal of Organic Chemistry;2022-09-02
2. Recent developments in green approaches for sustainable synthesis of indole-derived scaffolds;Molecular Diversity;2022-01-15
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