Iridium-catalyzed Asymmetric Hydrogenation of Polycyclic Pyrrolo/Indolo[1,2-a ]quinoxalines and Phenanthridines
Author:
Affiliation:
1. State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics; Chinese Academy of Sciences; Dalian 116023 Pepole's Republic of China
2. University of Chinese Academy of Sciences; Beijing 100049 Pepole's Republic of China
Funder
National Natural Science Foundation of China
Dalian Institute of Chemical Physics
Publisher
Wiley
Subject
General Chemistry
Reference81 articles.
1. Nanomolar Potency Pyrimido-pyrrolo-quinoxalinedione CFTR Inhibitor Reduces Cyst Size in a Polycystic Kidney Disease Model
2. Hit-to-lead optimization of pyrrolo[1,2-a]quinoxalines as novel cannabinoid type 1 receptor antagonists
3. Synthesis and evaluation of the antiproliferative activity of novel pyrrolo[1,2-a]quinoxaline derivatives, potential inhibitors of Akt kinase. Part II
4. Synthesis and antifungal activities of novel 5,6-dihydro-indolo[1,2-a]quinoxaline derivatives
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2. Synthesis of Carboranylated Dihydropyrrolo[1,2-a]quinoxalines and Dihydroindolo[1,2-a]quinoxalines by BF3·OEt2-Catalyzed Heterocyclization of C-Formyl-o-carboranes and Investigation of Their Oxidation Stability;The Journal of Organic Chemistry;2024-02-20
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5. Asymmetric Hydrogenation of Phenanthridines with Chiral Boranes;Chinese Journal of Chemistry;2023-12-08
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