Efficient Access to Arylated Aza‐ullazines by Regioselective Functionalization of their Pyridine Ring by H−Li Exchange and Electrophilic Substitution
Author:
Affiliation:
1. Université de Lorraine CNRS L2CM 57000 Metz France
2. Institut Jean Lamour UMR 7198 CNRS Université de Lorraine, Campus Artem 2 allée André Guinier, BP 50840 54011 Nancy Cedex France
3. Université de Lorraine CNRS, L2CM 54000 Nancy France
Funder
Université de Lorraine
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202100333
Reference32 articles.
1. Azulene-Based π-Functional Materials: Design, Synthesis, and Applications
2. Heterocyclic Nanographenes and Other Polycyclic Heteroaromatic Compounds: Synthetic Routes, Properties, and Applications
3. Molecular engineering of metal-free organic sensitizers with polycyclic benzenoid hydrocarbon donor for DSSC applications: The effect of the conjugate mode
4. 2 H ‐Dinaphthopentacene: A Polycyclic Aromatic Hydrocarbon Core for Metal‐Free Organic Sensitizers in Efficient Dye‐Sensitized Solar Cells
5. A Metal-Free N-Annulated Thienocyclopentaperylene Dye: Power Conversion Efficiency of 12 % for Dye-Sensitized Solar Cells
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1. Synthesis and Photophysical Evaluation of Dialkynyl‐N‐(het)arylpyrroles: Promising Key Compounds in Fluorescence Chemistry;Asian Journal of Organic Chemistry;2024-02-20
2. Recent Advance in the Synthesis of Ullazine and Its Derivatives;Chinese Journal of Organic Chemistry;2023
3. Efficient Access to Arylated Aza‐ullazines by Regioselective Functionalization of their Pyridine Ring by H−Li Exchange and Electrophilic Substitution;European Journal of Organic Chemistry;2021-06-14
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