Journal of Molecular Liquids, Год журнала: 2024, Номер 416, С. 126528 - 126528
Опубликована: Ноя. 18, 2024
Язык: Английский
Journal of Molecular Liquids, Год журнала: 2024, Номер 416, С. 126528 - 126528
Опубликована: Ноя. 18, 2024
Язык: Английский
ChemistrySelect, Год журнала: 2025, Номер 10(21)
Опубликована: Май 31, 2025
Abstract An expedited route to the synthesis of substituted 5‐(arylselanyl)‐1 H ‐pyrazoles and 5‐(arylthio)‐1 via reaction between 5‐amino‐1 bearing an electron withdrawing group (EWG) at C‐4 diaryl dichalcogenides in presence tert ‐butyl nitrite is described. The protocol compatible with substrates different EWGs, such as carboxylate, nitrile or phenylsulfonyl. strategy works even ‐1,2,3‐triazoles furnish corresponding chalcogenides. mechanism postulated involve a radical pathway.
Язык: Английский
Процитировано
0Beilstein Journal of Organic Chemistry, Год журнала: 2024, Номер 20, С. 1221 - 1235
Опубликована: Май 27, 2024
This article describes the detailed analysis of reaction between arylamines, such as aniline, o -anisidine, and methyl anthranilate, with selenium dioxide in acetonitrile. A systematic products help 77 Se NMR single-crystal X-ray crystallography revealed that progress follows three major pathways, electrophilic selenation, oxidative polymerization, solvent oxidation. For aniline predominant polymerization occurred, leading to formation respective polyaniline polymers products. was suppressed due delocalization amine lone pair electrons over adjacent carboxylate function, which prompted selenation pathway, two isomeric diorganyl selenides anthranilate. The diaryl were structurally characterized using diffraction. Density functional theory calculations suggest highest occupied molecular orbital anthranilate deeply buried, pathway. Due oxidation, oxamide also noticed a considerable extent. study provides utmost care must be exercised while SeO 2 an electrophile source aromatic substitution reactions.
Язык: Английский
Процитировано
1Molecules, Год журнала: 2024, Номер 29(22), С. 5365 - 5365
Опубликована: Ноя. 14, 2024
New approaches for the synthesis of organic thio- and selenocyanates, methods to incorporate them into more complex structures, including a wide variety heterocyclic polycylic derivatives, are reviewed. Protocols that convert SCN SeCN moieties thio seleno derivatives by transforming cyano group also examined. In representative cases, bioactivity data these classes compounds
Язык: Английский
Процитировано
1Tetrahedron, Год журнала: 2024, Номер unknown, С. 134434 - 134434
Опубликована: Дек. 1, 2024
Язык: Английский
Процитировано
1Journal of Molecular Liquids, Год журнала: 2024, Номер 416, С. 126528 - 126528
Опубликована: Ноя. 18, 2024
Язык: Английский
Процитировано
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