Synthesis of hybrid molecules based on thioglycolurils and 1,2,5-oxadiazoles via the Eschenmoser sulfide contraction Научная публикация
| Журнал |
Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436 |
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| Вых. Данные | Год: 2024, Том: 34, Номер: 1, Страницы: 122-125 Страниц : 4 DOI: 10.1016/j.mencom.2024.01.037 | ||
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Реферат:
A simple synthesis of novel hybrid molecules containing methylidenehexahydroimidazo[4,5-d]imidazol-2(1H)-one and 1,2,5-oxadiazole moieties is based on the Eschenmoser sulfide contraction involving alkylative precoupling of thioglycolurils with 3(4)-bromoacetyl-1,2,5-oxadiazoles. The proposed method does not require using toxic PPh3 for sulfur extrusion. The synthesized compounds may serve as platforms for constructing both new bioactive and new high- energy compounds.
Библиографическая ссылка:
Vinogradova E.E.
, Larin A.A.
, Gazieva G.A.
Synthesis of hybrid molecules based on thioglycolurils and 1,2,5-oxadiazoles via the Eschenmoser sulfide contraction
Mendeleev Communications. 2024. V.34. N1. P.122-125. DOI: 10.1016/j.mencom.2024.01.037 WOS Scopus OpenAlex
Synthesis of hybrid molecules based on thioglycolurils and 1,2,5-oxadiazoles via the Eschenmoser sulfide contraction
Mendeleev Communications. 2024. V.34. N1. P.122-125. DOI: 10.1016/j.mencom.2024.01.037 WOS Scopus OpenAlex
Идентификаторы БД:
| Web of science: | WOS:001181748400001 |
| Scopus: | 2-s2.0-85184906076 |
| OpenAlex: | W4391643481 |