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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2007 Volume 17, Issue 5, Pages 249–254 (Mi mendc3448)

This article is cited in 80 papers

Nucleophilic aromatic substitution of hydrogen and related reactions

V. N. Charushinab, O. N. Chupakhinab

a Department of Organic Chemistry, Urals State Technical University, Ekaterinburg, Russian Federation
b I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation

Abstract: The classical concept of nucleophilic aromatic substitution (SNAripso) has been complemented with a new synthetic methodology (SNH), enabling one to build new carbon–carbon C(sp2)–C(sp3), C(sp2)–C(sp2) and C(sp2)–C(sp) or carbon–heteroatom C(sp2)–X (X is O, N, P, S, halogen) bonds through nucleophilic displacement of hydrogen in an aromatic ring.

Language: English

DOI: 10.1016/j.mencom.2007.09.001



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