化学
催化作用
试剂
位阻效应
组合化学
溴化物
水介质
铃木反应
偶联反应
水溶液
有机化学
钯
作者
Shada Arun Dixith Reddy,Hari P. R. Mangunuru,Leila Terrab,Srinivasarao Tenneti,Nageswara Rao Kalikinidi,Santhosh Reddy Naini,Praveen Gajula,Emily B. Crull,Venumadhav Janganati,Raghavendra Kovvuri,N. Vasudevan,Daniel J. Lee,Jinya Yin,Lalith P. Samankumara,Rohit Mahar,Xueyi Zhang,Anji Chen,Chathuranga C. Hewa‐Rahinduwage,Zhirui Wang,Manasa Mamunooru
出处
期刊:Organic Letters
[American Chemical Society]
日期:2023-07-24
卷期号:26 (14): 2751-2757
被引量:3
标识
DOI:10.1021/acs.orglett.3c01663
摘要
We report a new class of highly effective, benzooxaphosphole-based, water-soluble ligands in the application of Suzuki–Miyaura cross-coupling reactions for sterically hindered substrates in aqueous media. The catalytic activities of the coupling reactions were greatly enhanced by the addition of catalytic amounts of organic phase transfer reagents, such as tetraglyme and tetrabutylammonium bromide. The optimized general protocol can be conducted with a low catalyst load, thereby providing a practical solution for these reactions. The viability of this new Suzuki–Miyaura protocol was demonstrated with various substrates to generate important building blocks, including heterocycles, for the synthesis of biologically active compounds.
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