Journal of Catalysis, Год журнала: 2023, Номер 427, С. 115098 - 115098
Опубликована: Авг. 19, 2023
Язык: Английский
Journal of Catalysis, Год журнала: 2023, Номер 427, С. 115098 - 115098
Опубликована: Авг. 19, 2023
Язык: Английский
Asian Journal of Organic Chemistry, Год журнала: 2024, Номер 13(5)
Опубликована: Фев. 29, 2024
Abstract A metal‐free [4+1] annulation of in‐situ generated ortho ‐quinone methides ( o ‐QMs) and CF 3 −imidoyl sulfoxonium ylides (TFISYs) has been achieved under mild conditions, which provides a facile straightforward access to variety trifluoromethyl‐containing 2,3‐dihydrobenzofurans in moderate excellent yields.
Язык: Английский
Процитировано
3Arabian Journal of Chemistry, Год журнала: 2024, Номер 17(8), С. 105845 - 105845
Опубликована: Май 23, 2024
Cyclopropenone has emerged as a highly versatile precursor in organic synthesis due to its diverse reactivity. The cyclopropenone derivatives could undergo various transformations such cycloaddition reactions, ring-opening and isomerization reactions the presence of different chemical reagents. Over years, significant progress been made manipulation cyclopropenones for construction carbocycles, heterocycles, other useful compounds. Despite several reviews that have concerned chemistry cyclopropenones, utility motifs carbocycles heterocycles rarely reported. Herein, we report recent advancements synthetic precursors towards compounds with biological significance.
Язык: Английский
Процитировано
3Tetrahedron, Год журнала: 2025, Номер unknown, С. 134454 - 134454
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
0The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Март 4, 2025
A catalyst and additive-free [2+1] annulation of 3-alkenyl-oxindoles with CF3-imidoyl sulfoxonium ylides (TFISYs) for the construction spiro 3,3'-cyclopropyl oxindoles has been achieved. cascade intermolecular Micheal-addition reaction intramolecular nucleophilic substitution sequence might be involved in transformation, which afforded a wide range multisubstituted oxindole products high efficiency diastereoselectivity.
Язык: Английский
Процитировано
0Journal of Catalysis, Год журнала: 2023, Номер 427, С. 115098 - 115098
Опубликована: Авг. 19, 2023
Язык: Английский
Процитировано
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