| Literature DB >> 25554781 |
Alexander Buitrago Santanilla1, Erik L Regalado1, Tony Pereira2, Michael Shevlin1, Kevin Bateman2, Louis-Charles Campeau1, Jonathan Schneeweis3, Simon Berritt1, Zhi-Cai Shi4, Philippe Nantermet5, Yong Liu1, Roy Helmy1, Christopher J Welch1, Petr Vachal6, Ian W Davies1, Tim Cernak7, Spencer D Dreher8.
Abstract
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.Entities:
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Year: 2014 PMID: 25554781 DOI: 10.1126/science.1259203
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728