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4,7-Functionalization of Tetradentate Phenanthroline Ligands via Nucleophilic Substitution of Fluorine Научная публикация

Журнал Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263
Вых. Данные Год: 2026, Том: 91, Номер: 1, Страницы: 302-315 Страниц : 14 DOI: 10.1021/acs.joc.5c02395
Авторы Zonov Roman V. 1 , Avagyan Nane A. 1 , Lemport Pavel S. 1 , Khrustalev Victor N. 2,3 , Roznyatovsky Vitaly A. 1 , Ustynyuk Yuri A. 1 , Nenajdenko Valentine G. 1
Организации
1 Department of Chemistry, Lomonosov Moscow State University, Leninskie gory 1 bld. 3, Moscow 119991, Russia
2 Peoples’ Friendship University of Russia (RUDN University), Miklukho-Maklay Str. 6, Moscow 117198, Russia
3 Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky Prospect 47, Moscow 119991, Russia

Информация о финансировании (1)

1 Институт органической химии им. Н. Д. Зелинского Российской академии наук

Реферат: An effective pathway for the functionalization of 1,10-phenanthroline-2,9-dicarboxamides (DAPhen) to positions 4 and 7 of the heterocyclic backbone by nucleophilic aromatic substitution was developed. The developed approach makes it possible to introduce various functional groups of almost any nature into positions 4 and 7 of the phenanthroline nucleus. The introduction of reactive functional groups, such as the azide group, has allowed for further functionalization. Thus, a set of novel symmetrically or unsymmetrically 4,7-disubstituted DAPhen ligands was prepared.
Библиографическая ссылка: Zonov R.V. , Avagyan N.A. , Lemport P.S. , Khrustalev V.N. , Roznyatovsky V.A. , Ustynyuk Y.A. , Nenajdenko V.G.
4,7-Functionalization of Tetradentate Phenanthroline Ligands via Nucleophilic Substitution of Fluorine
Journal of Organic Chemistry. 2026. V.91. N1. P.302-315. DOI: 10.1021/acs.joc.5c02395 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:001644816300001
Scopus: 2-s2.0-105027184359
OpenAlex: W7116663377
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