Supporting Information
All synthesized products were characterized by IR, NMR, GC–MS and elementary analysis. The data is reported in Supporting Information File 1, while copies of 1H and 13C NMR spectra are attached as Supporting Information File 2.
| Supporting Information File 1: Spectroscopic data of synthesized compounds. | ||
| Format: PDF | Size: 171.1 KB | Download |
| Supporting Information File 2: Copy of 1H and 13C NMR spectra of synthesized compounds. | ||
| Format: PDF | Size: 344.0 KB | Download |
Cite the Following Article
Easy and direct conversion of tosylates and mesylates into nitroalkanes
Alessandro Palmieri, Serena Gabrielli and Roberto Ballini
Beilstein J. Org. Chem. 2013, 9, 533–536.
https://doi.org/10.3762/bjoc.9.58
How to Cite
Palmieri, A.; Gabrielli, S.; Ballini, R. Beilstein J. Org. Chem. 2013, 9, 533–536. doi:10.3762/bjoc.9.58
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Scholarly Works
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- Ballini, R.; Palmieri, A. doi:10.1002/9783527826780.ch1
- Ballini, R.; Palmieri, A. Synthetic Procedures for the Preparation of Nitroalkanes. Advanced Synthesis & Catalysis 2018, 360, 2240–2266. doi:10.1002/adsc.201800163
- Mavratzotis, M.; Cassel, S.; Montaut, S.; Rollin, P. ω-Methylsulfanylalkyl Glucosinolates: A General Synthetic Pathway. Molecules (Basel, Switzerland) 2018, 23, 786. doi:10.3390/molecules23040786
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