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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2017, том 27, выпуск 2, страницы 160–162 (Mi mendc1930)

Эта публикация цитируется в 3 статьях

Communications

Dual reactivity of 1-chloro- and 1-bromo-3,5-dinitrobenzenes in aromatic nucleophilic substitution

M. D. Dutova, S. A. Sheveleva, V. N. Koshelevb, D. R. Aleksanyanb, O. V. Serushkinaa, O. D. Neverovaa, E. V. Kolvinab, E. S. Bobrovc

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b National University of Oil and Gas ‘Gubkin University’, Moscow, Russian Federation
c D.Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation


Аннотация: Aromatic nucleophilic substitution reactions in 1-halo-3,5-dinitrobenzenes (where the halogen is bromine or chlorine) can occur with replacement of either a nitro group or a halogen atom, depending on the nature of anionic nucleophile Nu as a Lewis base (hard, soft or intermediate), as well as on the polarity of the dipolar aprotic solvent.

Язык публикации: английский

DOI: 10.1016/j.mencom.2017.03.018



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