Chinese Chemical Letters, Год журнала: 2024, Номер unknown, С. 110539 - 110539
Опубликована: Окт. 1, 2024
Язык: Английский
Chinese Chemical Letters, Год журнала: 2024, Номер unknown, С. 110539 - 110539
Опубликована: Окт. 1, 2024
Язык: Английский
Tetrahedron, Год журнала: 2025, Номер 173, С. 134467 - 134467
Опубликована: Янв. 12, 2025
Язык: Английский
Процитировано
1Advanced Synthesis & Catalysis, Год журнала: 2024, Номер 366(14), С. 3050 - 3084
Опубликована: Май 22, 2024
Abstract Tetrahydro‐ β ‐carbolines (TH Cs) also known as tryptolines serve important structural elements in natural products and pharmaceutical compounds, they are utilized drug discovery. They display diverse bioactivities, including anticancer, antifungal, antiparasitic, anti‐ischemic, anti‐inflammatory, other activities. Besides their pharmacological biological significance, these motifs extensively used the production of bioactive compounds. This review is intended to summarize recent advancements chemistry this compound class, synthesis applications organic synthetic intermediates molecules.
Язык: Английский
Процитировано
5Tetrahedron Letters, Год журнала: 2025, Номер 156, С. 155451 - 155451
Опубликована: Янв. 4, 2025
Язык: Английский
Процитировано
0Tetrahedron, Год журнала: 2025, Номер unknown, С. 134632 - 134632
Опубликована: Март 1, 2025
Язык: Английский
Процитировано
0Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(18), С. 5306 - 5324
Опубликована: Янв. 1, 2024
This review summarizes recent achievements in electrosynthesis of organohalides through difunctionalization alkenes and alkynes provides insights into future directions for the development field.
Язык: Английский
Процитировано
2Organic & Biomolecular Chemistry, Год журнала: 2024, Номер unknown
Опубликована: Дек. 5, 2024
A novel electrochemical cyclization reaction of N -acryloyl-indole-3-carboxamides has been developed, which provides a new and efficient strategy for the synthesis γ-carbolinone derivatives.
Язык: Английский
Процитировано
2The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(8), С. 5619 - 5633
Опубликована: Апрель 5, 2024
Hydroxanthones have attracted considerable attention due to their significance in organic and biological chemistry, yet synthesis remains a great challenge. In this study, series of chromone-tethered alkenes are designed, radical cyclization reaction these chromone derivatives has been achieved under photoredox conditions. The uses bromodifluoroacetamides or bromodifluoroacetates as coupling partners, affording broad range functionalized tetrahydroxanthone products with up 85% yields. is triggered via the generation difluoroacetate radicals alkene cations fac-Ir(ppy)3 2,3,5,6-tetrakis(carbazol-9-yl)-1,4-dicyanobenzene photocatalyst. This approach offers access various from readily available starting materials enriches research content heteroarene-tethered alkenes.
Язык: Английский
Процитировано
1Tetrahedron, Год журнала: 2024, Номер 162, С. 134133 - 134133
Опубликована: Июль 3, 2024
Язык: Английский
Процитировано
1Chinese Chemical Letters, Год журнала: 2024, Номер unknown, С. 110539 - 110539
Опубликована: Окт. 1, 2024
Язык: Английский
Процитировано
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