Аннотация:
The substituent at the ortho position of the aryl groups of 5-chloro-3-aryl-2,1-benzisoxazoles is responsible for the ability of these structures to undergo rearrangements into acridinones under various conditions.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
V. Yu. Orlov, A. D. Kotov, V. V. Ganzha, V. G. Sokolov, “Participation of substituents at the ortho position of aryl groups in the rearrangements of 5-chloro-3-aryl-2,1-benzisoxazoles”, Mendeleev Commun., 14:1 (2004), 37–38
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3796
https://www.mathnet.ru/rus/mendc/v14/i1/p37
Эта публикация цитируется в следующих 4 статьяx:
A. D. Kotov, M. A. Prokaznikov, E. A. Antonova, A. I. Rusakov, “Synthesis of Nitrogen-Containing Heterocycles from Nitroarenes (Minireview)”, Chem Heterocycl Comp, 50:5 (2014), 647
Mieczysław Mąkosza, Krzysztof Wojciechowski, Topics in Heterocyclic Chemistry, 37, Metal Free C-H Functionalization of Aromatics, 2013, 51
V. Yu. Orlov, V. V. Ganzha, A. D. Kotov, V. G. Sokolov, “Synthesis of nitroacridinones from 2,1-benzisoxazole derivatives”, Russ J Org Chem, 43:10 (2007), 1502
Vladimir Yu. Orlov, Aleksandr D. Kotov, Valentin V. Ganzha, Vitaliy G. Sokolov, “Participation of Substituents at the ortho Position of Aryl Groups in the Rearrangements of 5‐Chloro‐3‐aryl‐2,1‐benzisoxazoles.”, ChemInform, 35:33 (2004)
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