Practical, scalable, and transition metal-free visible light-induced heteroarylation route to substituted oxindoles
Author:
Affiliation:
1. Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, Pennsylvania 19104-6323, USA
Abstract
Funder
National Science Foundation
National Institute of General Medical Sciences
National Institutes of Health
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/SC/D2SC05918E
Reference43 articles.
1. Oxindole: A chemical prism carrying plethora of therapeutic benefits
2. Oxindole and its derivatives: A review on recent progress in biological activities
3. Synthesis and Antitumor Effect in Vitro and in Vivo of Substituted 1,3-Dihydroindole-2-ones
4. Structure-Based Design of Spiro-oxindoles as Potent, Specific Small-Molecule Inhibitors of the MDM2−p53 Interaction
5. Spirooxindoles: Promising scaffolds for anticancer agents
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