Cu-Catalyzed Oxidative [3 + 2] Annulation of 2-(Pyridine-2-yl)acetates with Maleimides: Synthesis of 1H-Pyrrolo[3,4-b]indolizine-1,3-diones
Author:
Affiliation:
1. Key Laboratory of Medicinal Chemistry for Natural Resource (Yunnan University), Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming 650091, P. R. China
Funder
Natural Science Foundation of Yunnan Province
National Natural Science Foundation of China
Yunnan Province
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c01879
Reference44 articles.
1. Design, Synthesis, and Biological Evaluation of 1-(Indolizin-3-yl)ethan-1-ones as CBP Bromodomain Inhibitors for the Treatment of Prostate Cancer
2. Development of a Practical Synthesis of STA-5312, a Novel Indolizine Oxalylamide Microtubule Inhibitor
3. Synthesis, Anticonvulsant, and Anti-inflammatory Activities of Some New Benzofuran-Based Heterocycles
4. Indolizine: a biologically active moiety
5. Pyridine Activation via Copper(I)-Catalyzed Annulation toward Indolizines
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