A Directive Effect of Heterofunctions in Cyclocondensation Reactions of Acetylenylquinones with Hydrazine Научная публикация
Журнал |
Mendeleev Communications
ISSN: 0959-9436 , E-ISSN: 1364-551X |
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Вых. Данные | Год: 2000, Том: 10, Номер: 5, Страницы: 188-189 Страниц : 2 DOI: 10.1070/MC2000v010n05ABEH001353 | ||
Ключевые слова | HETEROCYCLIC SYNTHESIS; ACETYLENIC-COMPOUNDS; ROUTE | ||
Авторы |
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Организации |
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Реферат:
The heterocycle formed in the cyclocondensation reactions of 2-acetylenyl-1-chloro-9,10-anthraquinones or 5-acetylenyl-3-diethyl-amino-1,4-naphthoquinones with NH2NH2 is influenced by the presence of a heterofunction, e.g. a hydroxyl group, in the acetylenic substituent; this directive effect was used for the synthesis of naphtho[2,3-h]cinnoline-4,7,12-trione and 4H-naphtho[1,8-cd]-1,2-diazepin-8-one derivatives.
Библиографическая ссылка:
Barabanov I.I.
, Ivanchikova I.D.
, Shvartsberg M.S.
A Directive Effect of Heterofunctions in Cyclocondensation Reactions of Acetylenylquinones with Hydrazine
Mendeleev Communications. 2000. V.10. N5. P.188-189. DOI: 10.1070/MC2000v010n05ABEH001353 WOS Scopus РИНЦ CAPlusCA OpenAlex
A Directive Effect of Heterofunctions in Cyclocondensation Reactions of Acetylenylquinones with Hydrazine
Mendeleev Communications. 2000. V.10. N5. P.188-189. DOI: 10.1070/MC2000v010n05ABEH001353 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Опубликована в печати: | 1 янв. 2000 г. |
Поступила в редакцию: | 30 июн. 2000 г. |
Опубликована online: | 13 мар. 2008 г. |
Идентификаторы БД:
Web of science: | WOS:000089962000013 |
Scopus: | 2-s2.0-0040182779 |
РИНЦ: | 13349687 |
Chemical Abstracts: | 2000:745532 |
Chemical Abstracts (print): | 134:147578 |
OpenAlex: | W1985788320 |