Synthesis of Lactams by Isomerization of Oxindoles Substituted at C-3 by an ω-Amino Chain
Author:
Affiliation:
1. Chimie et photonique moléculaires, Institut des Sciences Chimiques de Rennes, Université de Rennes 1, CNRS-UMR 6226, Campus de Beaulieu, 35042 Rennes Cedex, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo501978j
Reference72 articles.
1. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids
2. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents
3. Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products
4. 3‐Alkenyl‐oxindoles: Natural Products, Pharmaceuticals, and Recent Synthetic Advances in Tandem/Telescoped Approaches
5. Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position
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