Collect. Czech. Chem. Commun.
1975, 40, 2816-2825
https://doi.org/10.1135/cccc19752816
The effect of solvent, base strength and isotopic substitution on the kinetics of nitro group rearrangement
V. Král and L. Lešetický
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- Micheletti G., Boga C., Pafundi M., Pollicino S., Zanna N.: New electron-donor and -acceptor architectures from benzofurazans and sym-triaminobenzenes: intermediates, products and an unusual nitro group shift. Org. Biomol. Chem. 2016, 14, 768. <https://doi.org/10.1039/C5OB02180D>
- Bianchi Lara, Ghelfi Franco, Giorgi Gianluca, Maccagno Massimo, Petrillo Giovanni, Spinelli Domenico, Stenta Marco, Tavani Cinzia: Uncommon 1,2‐Migration of a Nitro Group Within a β‐Nitrostyryl Moiety: Synthetic Scope and Mechanistic Details. Eur J Org Chem 2013, 2013, 6298. <https://doi.org/10.1002/ejoc.201300856>
- Cosimelli Barbara, Lamartina Liliana, Spinelli Domenico: On the reactivity of 3-bromo-2-nitrobenzo[ b ]thiophene with nucleophiles: elucidation of the base-catalysed mechanism with rearrangement. Tetrahedron 2001, 57, 8903. <https://doi.org/10.1016/S0040-4020(01)00875-4>
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- Spinelli Domenico, Zanirato Paolo, Di Miceli Elvira, Lamartina Liliana, Guerrera Francesco: On the Reaction of 3-Bromo-2-nitrobenzo[b]thiophene 13C-Labeled at C-2 with 3-(Trifluoromethyl)aniline: A Preliminary Insight into a Nucleophilic Substitution with Rearrangement. J. Org. Chem. 1997, 62, 4921. <https://doi.org/10.1021/jo962256m>
- KRAL V., LESETICKY L.: ChemInform Abstract: ISOMERISATION OF NITRO OLEFINS PART 3, EFFECT OF SOLVENT, BASE STRENGTHS AND ISOTOPIC SUBSTITUTION ON THE KINETICS OF NITRO GROUP REARRANGEMENT. Chemischer Informationsdienst 1975, 6. <https://doi.org/10.1002/chin.197549147>
