Loading Phlorins with Fullerenes by a [4 + 2]-Cycloaddition Reaction: Regulation of the Regioselectivity by Pyrrole Linkage Modes
Author:
Affiliation:
1. School of Science, Tianjin Chengjian University, Tianjin 300384, China
2. School of Chemistry and Molecular Engineering, East China University of Science & Technology, Shanghai 200237, China
Funder
Natural Science Foundation of Shanghai
Central University Basic Research Fund of China
Science and Technology Commission of Shanghai Municipality
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c02676
Reference44 articles.
1. Tetrapyrroles: the pigments of life
2. Molecular engineering strategies for fabricating efficient porphyrin-based dye-sensitized solar cells
3. Energy-Related Small Molecule Activation Reactions: Oxygen Reduction and Hydrogen and Oxygen Evolution Reactions Catalyzed by Porphyrin- and Corrole-Based Systems
4. Porphyrin-Based Nanomedicines for Cancer Treatment
5. Flexible Porphyrinoids
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2. Aromatic Ring-Fused Dipyrrins: Programmed [4 + 2]-Cycloaddition Pathway with Regio-selectivity upon Alkylamino-Substitution;The Journal of Organic Chemistry;2023-12-06
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