Recent progress in copper-free Sonogashira-Hagihara cross-couplings in water

被引:24
作者
Struwe, Julia [1 ]
Ackermann, Lutz [1 ]
Gallou, Fabrice [2 ]
机构
[1] Univ Gottingen, Wohler Res Inst Sustainable Chem, Inst Organ & Biomolekulare Chem r, D-37077 Gottingen, Germany
[2] Novartis Pharm AG, Chem & Analyt Dev, CH-4056 Basel, Switzerland
来源
CHEM CATALYSIS | 2023年 / 3卷 / 01期
基金
欧盟地平线“2020”;
关键词
C-H ALKYNYLATION; SUZUKI-MIYAURA COUPLINGS; PALLADIUM-CATALYZED REACTION; CARBON BOND FORMATION; ROOM-TEMPERATURE; ARYL BROMIDES; EFFICIENT PROTOCOL; MILD CONDITIONS; AQUEOUS-PHASE; PPM LEVELS;
D O I
10.1016/j.checat.2022.12.002
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The cross-coupling of terminal acetylenes for the construction of alkyne motives is a reaction type that is frequently required in the assembly of pharmaceuticals and natural products that use Sonogashira-Hagihara cross-coupling reactions. Although traditional procedures rely on the use of organic, usually hazardous, solvents with significant impact on the environment and humans, safer and more sustainable approaches have been developed in academia and industry during the last few years, and these rely on the use of water as green and non-hazardous reaction medium. This review first highlights the importance of Sonogashira-Hagihara couplings as well as micellar catalysis. Subsequently, the use of so-called benign-by-design surfactants in copper-free Sonogashira-Hagihara cross-couplings will be disclosed, before the focus is shifted to the use of other surfactants and co-solvents, as well as polymers. An outlook section proposes challenges and a potential future progress in this field.
引用
收藏
页数:18
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