A novel stereochemistry retention mechanism in the SN2 reaction

A recent study by Lu et al. reports the nucleophilic substitution reaction between Cl‒ and (CH3)3CI can proceed via a flip-over mechanism — a new type of SN2 pathway that retains configuration, discovered through simulations on a full-dimensional potential energy surface.

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Journal
Nature Communications
Published
2026-05-01
DOI
https://doi.org/10.1038/s41467-026-72120-5
Primary Topic
Chemical Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

A novel stereochemistry retention mechanism in the SN2 reaction

Jing Xie, Zhexuan Song, Hong Gao
Nature Communications
Chemical Reaction Mechanisms
article

A novel stereochemistry retention mechanism in the SN2 reaction

Jing Xie, Zhexuan Song, Hong Gao
article en

Abstract

A recent study by Lu et al. reports the nucleophilic substitution reaction between Cl‒ and (CH3)3CI can proceed via a flip-over mechanism — a new type of SN2 pathway that retains configuration, discovered through simulations on a full-dimensional potential energy surface.

Nature CommunicationsVol. 17(1)
Beijing Institute of Technology (CN), Beijing National Laboratory for Molecular Sciences (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 14%
Chemical Reaction Mechanisms
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