Supporting Information
| Supporting Information File 1: Characterization data, 1H and 13C NMR spectra of newly prepared porphyrin products. | ||
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Cite the Following Article
Unravelling a trichloroacetic acid-catalyzed cascade access to benzo[f]chromeno[2,3-h]quinoxalinoporphyrins
Chandra Sekhar Tekuri, Pargat Singh and Mahendra Nath
Beilstein J. Org. Chem. 2023, 19, 1216–1224.
https://doi.org/10.3762/bjoc.19.89
How to Cite
Tekuri, C. S.; Singh, P.; Nath, M. Beilstein J. Org. Chem. 2023, 19, 1216–1224. doi:10.3762/bjoc.19.89
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Scholarly Works
- Singh, A.; Nath, M. Cascade Radical Pathway-Enabled Nitrogen-Sulfur Coupling: Access to Isothiazolo[3,4-b]-meso-tetraarylporphyrins. The Journal of organic chemistry 2024, 89, 8610–8619. doi:10.1021/acs.joc.4c00548
- Singh, J.; Singh, A.; Nath, M. A divergent one-pot thiol-Michael strategy to create β-thiophene-fused porphyrins. Organic & biomolecular chemistry 2024, 22, 4369–4377. doi:10.1039/d4ob00598h
- Tsogoeva, S. B. Catalytic multi-step domino and one-pot reactions. Beilstein journal of organic chemistry 2024, 20, 254–256. doi:10.3762/bjoc.20.25
