Paper

Molecular mechanism of Hetero Diels-Alder reactions between (E)-1,1,1-trifluoro-3-nitrobut-2-enes and enamine systems in the light of Molecular Electron Density Theory.

Published Aug 23, 2020 · Agnieszka Kącka‐Zych, R. Jasiński

Journal of molecular graphics & modelling

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Abstract

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Study Snapshot

The molecular mechanism of Hetero Diels-Alder reactions between (E)-1,1,1-trifluoro-3-nitrobut-2-enes and enamine systems involves formation of zwitterionic structures in the first reaction stage, followed by three stages of bond breaks, pseudoradical

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Molecular mechanism of Hetero Diels-Alder reactions between (E)-1,1,1-trifluoro-3-nitrobut-2-enes and enamine systems in the light of Molecular Electron Density Theory.

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