Synthesis of 9-Phenanthrols through a Sequential Ligand-Free Suzuki/Intramolecular Friedel-Crafts Reaction and Their Cytotoxic Activity
Author:
Affiliation:
1. Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai, P. R. China
Funder
National Key R&D Program
National Natural Science Foundation of China
Shanghai Key Laboratory of Catalysis Technology for Polyolefins
Publisher
Informa UK Limited
Subject
Materials Chemistry,Organic Chemistry,Polymers and Plastics
Link
https://www.tandfonline.com/doi/pdf/10.1080/10406638.2020.1714674
Reference24 articles.
1. Natural phenanthrenes and their biological activity
2. Cytotoxic Phenanthrenes from the Rhizomes ofTamus communis
3. Spasmolytic stilbenoids from Maxillaria densa
4. The directed ortho metalation connection to aryl-aryl cross coupling.A general regiospecific synthesis of phenanthrols
5. The directed ortho metalation - palladium catalyzed cross coupling connection. A general regiospecific route to 9-phenanthrols and phenanthrenes. Exploratory further metalation
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1. A simple and convenient synthesis of labeled 9-hydroxy[ 13 C 6 ]phenanthrene as internal standard for mass spectrometry quantification of a key phenanthrene metabolite in human urines;Synthetic Communications;2023-12-06
2. α-Carbonyl Radicals from N-Enoxybenzotriazoles: De Novo Synthesis of 9-Phenanthrols;Organic Letters;2022-11-04
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