Nucleophilic substitution in the l-nitro-4-chloroanthraquinone by phenolates and thiophenolates

Nucleophilic substitution in the l-nitro-4-chloroanthraquinone by phenolates and thiophenolates Научная публикация

Журнал

Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393

Вых. Данные

Год: 1998, Том: 34, Номер: 6, Страницы: 861-866 Страниц : 6

Авторы

Tabatskaya A.A. ¹ , Beregovaya I.V. ¹ , Vlasov V.M. ¹

Организации

1	(Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Division, Russian Academy of Sciences, Novosibirsk, Russian Federation

In reactions of l-nitro-4-chloroanthraquinone with phenolate anions first is chiefly substituted the chlorine atom, whereas by the thiophenolate anion predominantly is replaced the nitro group. The difference in behavior with this substrate of the O- and S-nucleophiles is attributed to the change in the proportion of electrostatic and orbital interaction. © 1998 MAHK Hayka/Interperiodica Publishing.

Tabatskaya A.A. , Beregovaya I.V. , Vlasov V.M.
Nucleophilic substitution in the l-nitro-4-chloroanthraquinone by phenolates and thiophenolates
Russian Journal of Organic Chemistry. 1998. V.34. N6. P.861-866. Scopus РИНЦ

Scopus:	2-s2.0-22444455306
РИНЦ:	13297734

БД	Цитирований
Scopus	1
РИНЦ	1