Supporting Information
| Supporting Information File 1: Experimental details. | ||
| Format: PDF | Size: 5.5 MB | Download |
Cite the Following Article
Deoxygenative C2-heteroarylation of quinoline N-oxides: facile access to α-triazolylquinolines
Geetanjali S. Sontakke, Rahul K. Shukla and Chandra M. R. Volla
Beilstein J. Org. Chem. 2021, 17, 485–493.
https://doi.org/10.3762/bjoc.17.42
How to Cite
Sontakke, G. S.; Shukla, R. K.; Volla, C. M. R. Beilstein J. Org. Chem. 2021, 17, 485–493. doi:10.3762/bjoc.17.42
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Presentation Graphic
| Picture with graphical abstract, title and authors for social media postings and presentations. | ||
| Format: PNG | Size: 7.8 MB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Zhu, J.; Ji, Y.; He, X.; Han, B.; Zhao, Q. Exploring Synthetic Approaches for 2‐Aminoquinolines: Progress and Future Directions. European Journal of Organic Chemistry 2025, 28. doi:10.1002/ejoc.202500139
- Pal, K.; Dash, O. P.; Volla, C. M. R. Rhodium/selenium dual catalysis for accessing 2-aminopyrroles from N-sulfonyl-1,2,3-triazoles. Chemical communications (Cambridge, England) 2025, 61, 3872–3875. doi:10.1039/d4cc06346e
- Dhami, A.; Chandrasekharan, S. P.; Mohanan, K. BF3-Mediated C2-Amidation of Quinoline N-Oxides Employing Trifluorodiazoethane and Acetonitrile: Access to 2-N-(Trifluoroethyl)amidoquinolines. Organic letters 2024, 27, 180–185. doi:10.1021/acs.orglett.4c04127
- Ryu, H. K.; Song, Y. D.; Lee, J. H. Deoxygenation of N-heterocyclic N-oxides using isopropanol as a recyclable reductant. Organic Chemistry Frontiers 2024, 11, 2249–2268. doi:10.1039/d4qo00208c
- Garai, B.; Ali, M. R.; Mandal, R.; Sundararaju, B. Cp*Co(III)-Catalyzed C(8)-Nucleophilic Cascade Cyclization of Quinoline N-Oxide with 1,6-Enyne. Organic letters 2023, 25, 2018–2023. doi:10.1021/acs.orglett.3c00305
- Trouvé, J.; Gramage‐Doria, R. Destabilizing Predictive Copper‐Catalyzed Click Reactions by Remote Interactions with a Zinc‐Porphyrin Backbone. Helvetica Chimica Acta 2023, 106. doi:10.1002/hlca.202200191
- Badenock, J. C. Six-membered ring systems: pyridines and benzo derivatives. Progress in Heterocyclic Chemistry; Elsevier, 2023; pp 387–424. doi:10.1016/b978-0-443-18939-5.00012-3
- Singha, K.; Habib, I.; Hossain, M. Quinoline N‐Oxide: A Versatile Precursor in Organic Transformations. ChemistrySelect 2022, 7. doi:10.1002/slct.202203537
- Kadhim, M. M.; Abdulkareem Mahmood, E.; Poor Heravi, M. R.; Soleimani-Amiri, S.; Ebadi, A. G.; Vessally, E. The synthesis of biologically active 1-sulfonyl-1, 2, 3-triazoles from sulfonyl azides and alkynes: a focus review. Journal of Sulfur Chemistry 2022, 44, 377–391. doi:10.1080/17415993.2022.2149266
- Akyildiz, V.; Lafzi, F.; Kilic, H.; Saracoglu, N. Solvent-controlled regioselective C(5)-H/N(1)-H bond alkylations of indolines and C(6)-H bond alkylations of 1,2,3,4-tetrahydroquinolines with para-quinone methides. Organic & biomolecular chemistry 2022, 20, 3570–3588. doi:10.1039/d2ob00035k
- 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
- Thumpati, P.; Chakraborti, G.; Mandal, T.; Ravichandiran, V.; Dash, J. Cycloaddition of N-sulfonyl and N-sulfamoyl azides with alkynes in aqueous media for the selective synthesis of 1,2,3-triazoles. Green chemistry : an international journal and green chemistry resource : GC 2021, 24, 911–915. doi:10.1039/d1gc03340a
- Shukla, R. K.; Nair, A. M.; Volla, C. M. R. Allenes: Versatile Building Blocks in Cobalt-Catalyzed C–H Activation. Synlett 2021, 32, 1169–1178. doi:10.1055/a-1471-7307