Anchimeric assistance of the CO2CH3substituent in the elimination kinetics of 3-(methoxycarbonyl)propyl methanesulfonate in the gas phase
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1993/P2/P29930001295
Reference11 articles.
1. Regarding the mechanism of gas-phase dehydrohalogenation
2. Reexamination of the intimate ion pair mechanism in the gas phase pyrolysis kinetics of ethyl 4-bromobutyrate
3. The kinetics and mechanisms of the gas-phase pyrolysis of ethyl 4-bromobutyrate. The ion-pair mechanism revisited
4. The intimate ion pair mechanism in the maximally inhibited elimination kinetics of methyl 4-chlorobutyrate and methyl 5-chlorovalerate in the gas phase
5. Maximally inhibited pyrolysis kinetics of bromo esters in the gas phase. The ion pair mechanism
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1. Can a gas phase contact ion pair containing a hydrocarbon carbocation be formed in the ground state?;RSC Advances;2021
2. Pyrolysis of tert-Butyl tert-Butanethiosulfinate, t-BuS(O)St-Bu: A Computational Perspective of the Decomposition Pathways;The Journal of Physical Chemistry A;2011-03-18
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