Anticipating the Selectivity of Intramolecular Cyclization Reaction Pathways with Neural Network Potentials

Reaction mechanism search tools have demonstrated the ability to provide insights into likely products and rate-limiting steps of reacting systems. However, reactions involving several concerted bond changes─as can be found in many key steps of natural product syntheses─can complicate the search process. To mitigate these complications, we present a mechanism search strategy particularly suited to help expedite exploration of an exemplary family of such complex reactions, cyclizations. We provide a cost-effective strategy for identifying relevant elementary reaction steps by combining graph-based enumeration schemes and machine learning techniques for intermediate filtering. Key to this approach is our use of a neural network potential (NNP), AIMNet2-rxn, for computational evaluation of each candidate reaction pathway. In this article, we evaluate the NNP's ability to estimate activation energies, demonstrate the correct anticipation of stereoselectivity, and recapitulate complex enabling steps in natural product synthesis.

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Publication Details

Journal
Journal of Chemical Theory and Computation
Published
2025-10-09
DOI
https://doi.org/10.1021/acs.jctc.5c01161
Citations
2
Primary Topic
Machine Learning in Materials Science
Type
article
Field-Weighted Citation Impact
1.04
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article

Anticipating the Selectivity of Intramolecular Cyclization Reaction Pathways with Neural Network Potentials

Olexandr Isayev, Dylan M. Anstine, Connor W. Coley, Nicholas Casetti
2 citations
Journal of Chemical Theory and Computation
Machine Learning in Materials Science
1.04
article

Anticipating the Selectivity of Intramolecular Cyclization Reaction Pathways with Neural Network Potentials

Olexandr Isayev, Dylan M. Anstine, Connor W. Coley, Nicholas Casetti
article en
2 citations

Abstract

Reaction mechanism search tools have demonstrated the ability to provide insights into likely products and rate-limiting steps of reacting systems. However, reactions involving several concerted bond changes─as can be found in many key steps of natural product syntheses─can complicate the search process. To mitigate these complications, we present a mechanism search strategy particularly suited to help expedite exploration of an exemplary family of such complex reactions, cyclizations. We provide a cost-effective strategy for identifying relevant elementary reaction steps by combining graph-based enumeration schemes and machine learning techniques for intermediate filtering. Key to this approach is our use of a neural network potential (NNP), AIMNet2-rxn, for computational evaluation of each candidate reaction pathway. In this article, we evaluate the NNP's ability to estimate activation energies, demonstrate the correct anticipation of stereoselectivity, and recapitulate complex enabling steps in natural product synthesis.

Journal of Chemical Theory and ComputationVol. 21(20)
Massachusetts Institute of Technology (US), Carnegie Mellon University (US)
Openalex Percentile: Top 22%
Machine Learning in Materials Science
1.04
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