A convenient approach to diastereomerically pure 1,3,4-trisubstituted pyrrolidin-2-ones by intramolecular cyclisation of N-(2-alken-1-yl)amides mediated by Mn(III). An entry to both (R)- and (S)-3-pyrrolidineacetic acid
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Manganese( III ) Acetate‐Mediated Cyclizations;Manganese Catalysis in Organic Synthesis;2021-09-12
2. Enantioselective Three-Step Synthesis of Homo-β-proline: A Donor–Acceptor Cyclopropane as Key Intermediate;Organic Letters;2017-05-09
3. Asymmetric Allylic Amination of Morita-Baylis-Hillman Carbonates with Silylated tert -Butylhydroxycarbamate Derivatives;European Journal of Organic Chemistry;2017-04-10
4. Redox-Neutral Palladium-Catalyzed C–H Functionalization To Form Isoindolinones with Carboxylic Acids or Anhydrides as Readily Available Starting Materials;Organic Letters;2015-05-15
5. A convenient synthesis of 3,4-cis-disubstituted pyrrolidin-2-ones;Tetrahedron Letters;2015-01
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