Synthesis of 14π-electron peri-annelated tricyclic heteroaromatic systems based on 2,4,6-trinitrotoluene

Synthesis of 14π-electron peri-annelated tricyclic heteroaromatic systems based on 2,4,6-trinitrotoluene Научная публикация

Журнал

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Вых. Данные

Год: 2002, Том: 12, Номер: 5, Страницы: 200-201 Страниц : 2 DOI: 10.1070/mc2002v012n05abeh001642

Авторы

Starosotnikov Aleksei M. ¹ , Vinogradov Vasilii M. ¹ , Shevelev Svyatoslav A. ¹

Организации

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Methyl 1-aryl-7-nitro-1H-thiopyrano[4,3,2-cd]indazol-4-carboxylates 2 and 1,5-diaryl-7-nitro-1,5-dihydropyrazolo[3,4,5-de]- cinnolines 4 were prepared based on 1-aryl-3-formyl-4,6-dinitro-1H-indazoles 1, which were synthesised previously starting from 2,4,6-trinitrotoluene.

Starosotnikov A.M. , Vinogradov V.M. , Shevelev S.A.
Synthesis of 14π-electron peri-annelated tricyclic heteroaromatic systems based on 2,4,6-trinitrotoluene
Mendeleev Communications. 2002. V.12. N5. P.200-201. DOI: 10.1070/mc2002v012n05abeh001642 WOS Scopus OpenAlex

Web of science:	WOS:000179887800016
Scopus:	2-s2.0-0036764340
OpenAlex:	W2140736591

БД	Цитирований
OpenAlex	6
Scopus	5
Web of science	6