化学
胺化
组合化学
偶联反应
过程(计算)
纳米技术
材料化学
有机化学
催化作用
生化工程
计算机科学
绿色化学
工程类
材料科学
反应机理
操作系统
作者
Balaram S. Takale,Fanyi Kong,Ruchita R. Thakore
出处
期刊:Organics
[Multidisciplinary Digital Publishing Institute]
日期:2022-01-18
卷期号:3 (1): 1-21
被引量:12
摘要
Cross-coupling reactions have changed the way complex molecules are synthesized. In particular, Suzuki–Miyaura and Buchwald–Hartwig amination reactions have given opportunities to elegantly make pharmaceutical ingredients. Indeed, these reactions are at the forefront of both the stages of drug development, medicinal chemistry, and process chemistry. On the one hand, these reactions have given medicinal chemists a resource to derivatize the core compound to arrive at scaffold rapidly. On the other hand, these cross couplings have offered the process chemists a smart tool to synthesize the development candidates safely, quickly, and efficiently. Generally, the application of cross-coupling reactions is broad. This review will specifically focus on their real (pharma) world applications in large-scale synthesis appearing in the last three years.
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