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Grzybowski, Bartosz A.
School of Natural Science
Research Interests
  • Nano science
  • Nanomaterials
  • Programmable Reactions
  • Chemical Networks
  • Cellular Dynamics

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Computational planning of the synthesis of complex natural products

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Title
Computational planning of the synthesis of complex natural products
Author
Mikulak-Klucznik, BarbaraGolebiowska, PatrycjaBayly, Alison A.Popik, OskarKlucznik, TomaszSzymkuc, SaraGajewska, Ewa P.Dittwald, PiotrStaszewska-Krajewska, OlgaBeker, WiktorBadowski, TomaszScheidt, Karl A.Molga, KarolMlynarski, JacekMrksich, MilanGrzybowski, Bartosz A.
Issue Date
2020-12
Publisher
NATURE RESEARCH
Citation
NATURE, v.588, no.7836, pp.83 - 88
Abstract
Training algorithms to computationally plan multistep organic syntheses has been a challenge for more than 50 years(1-7). However, the field has progressed greatly since the development of early programs such as LHASA(1,7), for which reaction choices at each step were made by human operators. Multiple software platforms(6,8-14) are now capable of completely autonomous planning. But these programs 'think' only one step at a time and have so far been limited to relatively simple targets, the syntheses of which could arguably be designed by human chemists within minutes, without the help of a computer. Furthermore, no algorithm has yet been able to design plausible routes to complex natural products, for which much more far-sighted, multistep planning is necessary(15,16) and closely related literature precedents cannot be relied on. Here we demonstrate that such computational synthesis planning is possible, provided that the program's knowledge of organic chemistry and data-based artificial intelligence routines are augmented with causal relationships(17,18), allowing it to 'strategize' over multiple synthetic steps. Using a Turing-like test administered to synthesis experts, we show that the routes designed by such a program are largely indistinguishable from those designed by humans. We also successfully validated three computer-designed syntheses of natural products in the laboratory. Taken together, these results indicate that expert-level automated synthetic planning is feasible, pending continued improvements to the reaction knowledge base and further code optimization. A synthetic route-planning algorithm, augmented with causal relationships that allow it to strategize over multiple steps, can design complex natural-product syntheses that are indistinguishable from those designed by human experts.
URI
https://scholarworks.unist.ac.kr/handle/201301/49101
URL
https://www.nature.com/articles/s41586-020-2855-y
DOI
10.1038/s41586-020-2855-y
ISSN
0028-0836
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