自动化
化学
药物发现
纳米技术
生化工程
时间轴
组合化学
计算机科学
工艺工程
吞吐量
有机化学
材料科学
工程类
历史
考古
机械工程
电信
生物化学
无线
作者
A. Buitrago Santanilla,Erik L. Regalado,Tony Pereira,Michael Shevlin,Kevin P. Bateman,Louis‐Charles Campeau,Jonathan E. Schneeweis,Simon Berritt,Zhicai Shi,Philippe G. Nantermet,Yong Liu,Roy Helmy,Christopher J. Welch,Petr Váchal,Ian W. Davies,Tim Cernak,Spencer D. Dreher
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2015-01-02
卷期号:347 (6217): 49-53
被引量:476
标识
DOI:10.1126/science.1259203
摘要
At the forefront of new synthetic endeavors, such as drug discovery or natural product synthesis, large quantities of material are rarely available and timelines are tight. A miniaturized automation platform enabling high-throughput experimentation for synthetic route scouting to identify conditions for preparative reaction scale-up would be a transformative advance. Because automated, miniaturized chemistry is difficult to carry out in the presence of solids or volatile organic solvents, most of the synthetic "toolkit" cannot be readily miniaturized. Using palladium-catalyzed cross-coupling reactions as a test case, we developed automation-friendly reactions to run in dimethyl sulfoxide at room temperature. This advance enabled us to couple the robotics used in biotechnology with emerging mass spectrometry-based high-throughput analysis techniques. More than 1500 chemistry experiments were carried out in less than a day, using as little as 0.02 milligrams of material per reaction.
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