Synthesis of a Family of Highly Substituted Porphyrin Thioethers via Nitro Displacement in 2,3,7,8,12,13,17,18-Octaethyl-5,10,15,20-tetranitroporphyrin
Author:
Affiliation:
1. School of Chemistry, SFI Tetrapyrrole Laboratory, Trinity Biomedical Sciences Institute, Trinity College Dublin, The University of Dublin, 152-160 Pearse Street, Dublin 2, Ireland
Funder
Science Foundation Ireland
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b00328
Reference62 articles.
1. Nucleophilic Substitution as a Tool for the Synthesis of Unsymmetrical Porphyrins
2. Nucleophilic substitution of meso-nitrooctaethylporphyrins
3. Aggregation properties of nitroporphyrins: comparisons between solid-state and solution structures
4. Prevention of out-of-plane macrocycle distortion by thallium in the sterically strained 2,3,7,8,12,13,17,18-octaethyl-5,10,15,20-tetranitroporphyrin
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