Synthesis of Trifluoromethyl-Substituted [14]Triphyrin(2.1.1), Its Selective Reduction to Triphachlorin, and Stable Isomeric Triphabacteriochlorins via Direct Detrifluoromethylation
Author:
Affiliation:
1. School of Chemistry, University of Hyderabad, Hyderabad 500046, India
Funder
Science and Engineering Research Board
University of Hyderabad
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c03653
Reference38 articles.
1. Gouterman, M., Dolphin, D., Eds. Porphyrins: Optical spectra and electronic structure of porphyrins and related rings; Academic Press: Boston, 1978; Vol. 3, Part A, pp 1–165.
2. The Structure and Chemistry of Functional Groups**Contribution No. 216 from the Charles F. Kettering Research Laboratory, Yellow Springs, Ohio. The preparation of this chapter was supported in part by National Science Foundation Grant No. GB-2089.
3. Chlorophyll.
4. Proposed structure for the prosthetic group of the catalase HPII from Escherichia coli
5. Siroheme: A New Prosthetic Group Participating in Six-Electron Reduction Reactions Catalyzed by Both Sulfite and Nitrite Reductases
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1. Synthesis of unsymmetrical 2,3,7,8-tetrabromo meso-5,10,11,16-tetraaryl- triphyrin(2.1.1) and its use in the synthesis of sterically crowded 2,3,5,7,8,10,11,16-octaarylated triphyrin(2.1.1)s;Organic & Biomolecular Chemistry;2024
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