Aromatic Nucleophilic Denitrocyclization Reactions

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  • S. Radl Research Institute for Pharmacy and Biochemistry, Prague

Abstrakt

Sufficiently activated aromatic nitro groups are known to undergo replacement with various nucleophiles. Intramolecular version of this reaction is called aromatic denitrocyclization reaction. Five-, six-, seven-, and even eight-membered rings are formed with oxygen, sulfur, nitrogen, and carbon nucleophiles involved. The present review covers the most important reactions of this type, such as the Turpin reaction and similar methods of preparation leading to phenothiazines, dihydrophenazines, dithiines, and dioxines, as well as some less frequent interesting reactions of this type.

Publikováno

15.10.2001

Jak citovat

Radl, S. (2001). Aromatic Nucleophilic Denitrocyclization Reactions. Chemické Listy, 95(9). Získáno z http://www.chemicke-listy.cz/ojs3/index.php/chemicke-listy/article/view/2386

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