Organic & Biomolecular Chemistry, Год журнала: 2023, Номер 22(3), С. 486 - 490
Опубликована: Дек. 13, 2023
In contrast to the previously reported intramolecular aryl migration, we present selective sulfenylation of
Язык: Английский
Organic & Biomolecular Chemistry, Год журнала: 2023, Номер 22(3), С. 486 - 490
Опубликована: Дек. 13, 2023
In contrast to the previously reported intramolecular aryl migration, we present selective sulfenylation of
Язык: Английский
Organic Letters, Год журнала: 2024, Номер 26(9), С. 1985 - 1990
Опубликована: Фев. 23, 2024
Herein, we disclosed a highly chemoselective synthesis of quinoline-2-one and quinoline-2-thione derivatives using EtOS2K as the C1 source. Quinoline-2-one were synthesized selectively with NaCl catalyst in solvent DMSO/H2O, while produced without need for any an environmentally friendly EtOH/H2O. The reaction conditions mild had good functional group tolerance.
Язык: Английский
Процитировано
2Beilstein Journal of Organic Chemistry, Год журнала: 2024, Номер 20, С. 841 - 851
Опубликована: Апрель 18, 2024
Cyclic annulation involving diaryliodonium salts is an efficient tool for the construction of two or more chemical bonds in a one-pot process.
Язык: Английский
Процитировано
2Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(19), С. 5558 - 5563
Опубликована: Янв. 1, 2024
A simple, general, thiol- and metal-free method for the synthesis of symmetrical unsymmetrical polyfluorodiaryl sulfides polyfluoroaryl-alkyl sulfides.
Язык: Английский
Процитировано
2Chemical Science, Год журнала: 2023, Номер 14(34), С. 9197 - 9206
Опубликована: Янв. 1, 2023
Electrophilic xanthylation of C/O/N nucleophiles via powerful N -xanthylphthalimides was investigated, with standout features broad substrate scope, excellent tolerance and late-stage functionalization bioactive or functional molecules.
Язык: Английский
Процитировано
5Organic & Biomolecular Chemistry, Год журнала: 2023, Номер 22(3), С. 486 - 490
Опубликована: Дек. 13, 2023
In contrast to the previously reported intramolecular aryl migration, we present selective sulfenylation of
Язык: Английский
Процитировано
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