Metal-Free Switchable Chemo- and Regioselective Alkylation of Oxindoles Using Secondary Alcohols
Author:
Affiliation:
1. Department of Chemistry, SS Bhatnagar Block, Indian Institute of Technology Ropar, Punjab140001, India
Funder
Indian Institute of Technology Ropar
Science and Engineering Research Board
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00903
Reference45 articles.
1. The Chemistry of Oxindole.
2. Structure-Based Design of Spiro-oxindoles as Potent, Specific Small-Molecule Inhibitors of the MDM2−p53 Interaction
3. Synthesis and Antitumor Effect in Vitro and in Vivo of Substituted 1,3-Dihydroindole-2-ones
4. Recent Developments in the C(sp3 )−H Functionalization of 2-Oxindoles through Radical Reactions
5. Development of Synthetic Methodologies via Catalytic Enantioselective Synthesis of 3,3-Disubstituted Oxindoles
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