Organic Letters, Год журнала: 2024, Номер unknown
Опубликована: Дек. 17, 2024
The installation of
Язык: Английский
Organic Letters, Год журнала: 2024, Номер unknown
Опубликована: Дек. 17, 2024
The installation of
Язык: Английский
Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(10), С. 2897 - 2904
Опубликована: Янв. 1, 2024
Cyclization and 1,4-conjugate addition/cyclization between 2-activated 1,3-enynes azlactones were achieved with chiral guanidine-amides for enol-type activation to yield a range of δ-lactone derivatives.
Язык: Английский
Процитировано
9The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Апрель 18, 2025
A Pd-catalyzed protocol that provides efficient access to acyclic 1,2-dioxygenated dienes has been established. The installation of the bifunctional carbonate electrofuge diene cores enabled such undergo a regioselective decarboxylative Diels-Alder cycloaddition/aromatization reaction, affording diverse synthetic challenging multisubstituted phenols with ease.
Язык: Английский
Процитировано
0Molecules, Год журнала: 2025, Номер 30(8), С. 1832 - 1832
Опубликована: Апрель 19, 2025
A novel method for the efficient and straightforward synthesis of tetrasubstituted furans is presented, employing a base-catalyzed reaction α-hydroxy ketones cyano compounds. The proceeds under relatively mild conditions, utilizes readily available starting materials, exhibits good functional group tolerance high yields. Notably, this obviates need expensive metal catalysts introduces crucial groups such as amino moieties. Furthermore, it avoids prerequisite functionalization substrates, thereby enhancing atomic economy.
Язык: Английский
Процитировано
0Molecules, Год журнала: 2024, Номер 29(16), С. 3904 - 3904
Опубликована: Авг. 18, 2024
Ketones are ubiquitous patterns found in various biological molecules and natural products. In recent years, a number of acylation methods have been developed based on the use α-oxocarboxylic acids as acyl-transfer reagents, with particular emphasis photoinduced decarboxylative
Язык: Английский
Процитировано
1Green Chemistry, Год журнала: 2024, Номер 26(21), С. 10804 - 10810
Опубликована: Янв. 1, 2024
We present an efficient and sustainable protocol for the photoinduced-radical hydrocyclization of isocyanides, providing a united route to assemble diverse α-unsubstituted N-heteroarenes.
Язык: Английский
Процитировано
1Organic & Biomolecular Chemistry, Год журнала: 2024, Номер unknown
Опубликована: Дек. 3, 2024
The present review focuses on recent progress (2020–2024) in the visible-light-driven decarboxylative cyclization of various carboxylic acid derivatives for constructing carbo-/heterocycles.
Язык: Английский
Процитировано
1Organic Letters, Год журнала: 2024, Номер unknown
Опубликована: Дек. 17, 2024
The installation of
Язык: Английский
Процитировано
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