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Characteristic features of nucleophilic substitution in the series of 4-RSO2-6-nitro-1-phenyl-1H-indazoles and benzo[d]isoxazoles Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Вых. Данные Год: 2003, Том: 52, Номер: 8, Страницы: 1797-1799 Страниц : 3 DOI: 10.1023/a:1026012922607
Авторы Starosotnikov A.M. 1 , Shevelev S.A. 1
Организации
1 N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow (Russian Federation)

Реферат: Oxidation of 3-substituted 4-R-6-nitro-1-phenyl-1H-indazoles and benzo[d]isoxazoles (R = Ph, CH2CO2Me) gave the corresponding sulfones treatment of which with PhSH—K2CO3 in N-methylpyrrolidone results in replacement of only the RSO2 group in position 4 with the 6-NO2 group remaining intact, contrary to the known sequence of nucleophilic substitution for meta-arranged nucleofuges.
Библиографическая ссылка: Starosotnikov A.M. , Shevelev S.A.
Characteristic features of nucleophilic substitution in the series of 4-RSO2-6-nitro-1-phenyl-1H-indazoles and benzo[d]isoxazoles
Russian Chemical Bulletin. 2003. V.52. N8. P.1797-1799. DOI: 10.1023/a:1026012922607 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000186446500022
Scopus: 2-s2.0-0346373483
OpenAlex: W2949112406
Цитирование в БД:
БД Цитирований
OpenAlex 6
Scopus 4
Web of science 6
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