Late-Stage Chemo- and Enantioselective Oxidation of Indoles to C3-Monosubstituted Oxindoles
Author:
Affiliation:
1. School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China
2. Shenzhen Research Institute of Shandong University, Shenzhen 518057, China
Funder
Taishan Scholar Project of Shandong Province
National Natural Science Foundation of China
Shenzhen Special Funds
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.3c11742
Reference81 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. Oxindole: A chemical prism carrying plethora of therapeutic benefits
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