File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

GrzybowskiBartosz Andrzej

Grzybowski, Bartosz A.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Closed-loop optimization of general reaction conditions for heteroaryl Suzuki-Miyaura coupling

Author(s)
Angello, Nicholas H.Rathore, VandanaBeker, WiktorWolos, AgnieszkaJira, Edward R.Roszak, RafalWu, Tony C.Schroeder, Charles M.Aspuru-Guzik, AlanGrzybowski, Bartosz A.Burke, Martin D.
Issued Date
2022-10
DOI
10.1126/science.adc8743
URI
https://scholarworks.unist.ac.kr/handle/201301/61134
Citation
SCIENCE, v.378, no.6618, pp.399 - 405
Abstract
General conditions for organic reactions are important but rare, and efforts to identify them usually consider only narrow regions of chemical space. Discovering more general reaction conditions requires considering vast regions of chemical space derived from a large matrix of substrates crossed with a high-dimensional matrix of reaction conditions, rendering exhaustive experimentation impractical. Here, we report a simple closed-loop workflow that leverages data-guided matrix down-selection, uncertainty-minimizing machine learning, and robotic experimentation to discover general reaction conditions. Application to the challenging and consequential problem of heteroaryl Suzuki-Miyaura cross-coupling identified conditions that double the average yield relative to a widely used benchmark that was previously developed using traditional approaches. This study provides a practical road map for solving multidimensional chemical optimization problems with large search spaces.
Publisher
AMER ASSOC ADVANCEMENT SCIENCE
ISSN
0036-8075
Keyword
PROTODEBORONATIONDIGITIZATIONCHEMISTRYDIVERSESYSTEM

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.