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Mendeleev Communications, 2004, Volume 14, Issue 5, Pages 217–219
DOI: https://doi.org/10.1070/MC2004v014n05ABEH001876
(Mi mendc3884)
 

This article is cited in 1 scientific paper (total in 1 paper)

Influence of the nucleophile structure on the selectivity of the nitro group and fluorine displacement in SNAr reactions

I. A. Khalfina, V. M. Vlasov

N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
Full-text PDF (221 kB) Citations (1)
Abstract: Temperature-dependent measurements according to the modified Eyring equation allowed the evaluation of the displacement selectivity of the nitro group and fluorine in the SNAr reactions of 3-nitro-5-R-benzotrifluorides (R = NO2, F) with the nucleophiles (2ArYH)·K2CO3 and ArY−K+ (Y = O, S) in DMF solutions.
Document Type: Article
Language: English


Citation: I. A. Khalfina, V. M. Vlasov, “Influence of the nucleophile structure on the selectivity of the nitro group and fluorine displacement in SNAr reactions”, Mendeleev Commun., 14:5 (2004), 217–219
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  • https://www.mathnet.ru/eng/mendc3884
  • https://www.mathnet.ru/eng/mendc/v14/i5/p217
  • This publication is cited in the following 1 articles:
    1. Donald W. Boerth, Anthony C. Arvanites, “Nucleophilic aromatic substitution in chlorinated aromatic systems with a glutathione thiolate model”, J. Phys. Org. Chem., 30:7 (2017), e3640  crossref
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