Gas-Phase Identity Nucleophilic Substitution Reactions of Cyclopropenyl Halides
Author:
Affiliation:
1. Department of Chemistry, Inha University, Inchon 402-751, Korea
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0164047
Reference58 articles.
1. An ab initio study of model SN2 reactions with inclusion of electron correlation effects through second-order Moeller-Plesset perturbation calculations
2. Theoretical study of potential wells and barriers for SN2 rearrangement in the systems (XCH3X)- with X = F, Cl, and Br
3. A six-body potential energy surface for the SN2 reaction Cl-(g) + CH3Cl(g) and a variational transition-state-theory calculation of the rate constant
4. Trajectory studies ofSN2 nucleophilic substitution. II. Nonstatistical central barrier recrossing in the Cl−+CH3Cl system
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