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| Supporting Information File 3: Crystallographic data for compound 3e. | ||
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Cite the Following Article
Synthesis of β-triazolylenones via metal-free desulfonylative alkylation of N-tosyl-1,2,3-triazoles
Soumyaranjan Pati, Renata G. Almeida, Eufrânio N. da Silva Júnior and Irishi N. N. Namboothiri
Beilstein J. Org. Chem. 2021, 17, 762–770.
https://doi.org/10.3762/bjoc.17.66
How to Cite
Pati, S.; Almeida, R. G.; da Silva Júnior, E. N.; Namboothiri, I. N. N. Beilstein J. Org. Chem. 2021, 17, 762–770. doi:10.3762/bjoc.17.66
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Scholarly Works
- Elgemeie, G. H.; Azzam, R. A.; Zaghary, W. A.; Aly, A. A.; Metwally, N. H.; Sarhan, M. O.; Abdelhafez, E. M.; Elsayed, R. E. Synthesis, chemistry and uses of N-sulfonated N-triazoles and N-tetrazoles. N-Sulfonated-N-Heterocycles; Elsevier, 2022; pp 179–252. doi:10.1016/b978-0-12-822179-2.00005-7
- Xing, Q.; Zhou, C.; Jiang, S.; Chen, S.; Deng, G.-J. Acid-catalyzed three-component addition of carbonyl compounds with 1,2,3-triazoles and indoles. Organic & biomolecular chemistry 2021, 19, 7838–7842. doi:10.1039/d1ob01451j
