Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(4), С. 1218 - 1218
Опубликована: Янв. 1, 2024
摘要 2-亚甲基-2,3-二氢苯并呋喃衍生物作为多种天然产物及药物的核心骨架之一, 寻找由简便易得原料有效合成 2-亚甲基-2,3-二氢苯并呋喃的新方法具有重要的意义.开发了一种新的银催化邻羟基苯基炔丙醇的 5-exo
Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(4), С. 1218 - 1218
Опубликована: Янв. 1, 2024
摘要 2-亚甲基-2,3-二氢苯并呋喃衍生物作为多种天然产物及药物的核心骨架之一, 寻找由简便易得原料有效合成 2-亚甲基-2,3-二氢苯并呋喃的新方法具有重要的意义.开发了一种新的银催化邻羟基苯基炔丙醇的 5-exo
Journal of the American Chemical Society, Год журнала: 2024, Номер 146(2), С. 1722 - 1731
Опубликована: Янв. 4, 2024
Herein, we report a ligand-controlled palladium-catalyzed method that enables the synthesis of ynones and γ-butenolides with excellent regioselectivity from same set readily available aryl iodides, acetylenes, BrCF2CO2K. In this reaction, [PdII]═CF2 does demonstrate electrophilicity can generate CO when reacting H2O. It is environmentally friendly safe compared to traditional methods, current protocol us afford in high yields functionality tolerance. Moreover, esters also be obtained corresponding phenols alcohols utilizing strategy. The success late-stage functionalization bioactive compounds further illustrates synthetic utility material development drug discovery.
Язык: Английский
Процитировано
19The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Март 24, 2025
We have developed a palladium-catalyzed ester carbonylation reaction that enables the synthesis of ester-substituted benzofuran derivatives in single step through introduction alkyl halides undergoing situ hydrolysis and alkynyl aryl iodides. This method demonstrates broad applicability to both primary secondary while maintaining excellent functional group compatibility under low palladium loading conditions. Notably, this strategy significantly expands scope reactions.
Язык: Английский
Процитировано
1Chemical Communications, Год журнала: 2024, Номер 60(65), С. 8613 - 8616
Опубликована: Янв. 1, 2024
A palladium-catalyzed enantioselective intramolecular Heck cyclization/carbonylation reaction has been developed, which utilizes formates as the source of CO to enantioselectively synthesize ester-substituted indolo[2,1- a ]isoquinolines.
Язык: Английский
Процитировано
2Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(4), С. 1218 - 1218
Опубликована: Янв. 1, 2024
摘要 2-亚甲基-2,3-二氢苯并呋喃衍生物作为多种天然产物及药物的核心骨架之一, 寻找由简便易得原料有效合成 2-亚甲基-2,3-二氢苯并呋喃的新方法具有重要的意义.开发了一种新的银催化邻羟基苯基炔丙醇的 5-exo
Процитировано
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