Inversion vs Retention of Configuration in Gas-Phase Ammonium Ion/Alcohol Reactions
Author:
Affiliation:
1. Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, 610 Taylor Road, Piscataway, New Jersey 08854
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo016267d
Reference19 articles.
1. How Persistent Is Cyclopropyl upon Nucleophilic Substitution, and Is Frontside Displacement Possible? A Model Study
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1. Organic Reactions of Anions;Computational Organic Chemistry;2014-03-01
2. Nucleophilic identity substitution reactions. The reaction between water and protonated alcoholsPart I. For Part II, see following paper (DOI: 10.1039/b302270f).Electronic supplementary information (ESI) available: Cartesian co-ordinates for all species together with analytical imaginary frequencies for the transition structures. See http://www.rsc.org/suppdata/ob/b3/b302268d/;Organic & Biomolecular Chemistry;2003
3. Physical organic chemistry of the gas phase. Reactivity trends for organic cations;TOP CURR CHEM;2003
4. Reaction of imidazole with toluene-4-sulfonate salts of substituted phenyl N-methylpyridinium-4-carboxylate esters: special base catalysis by imidazole;Organic & Biomolecular Chemistry;2003
5. Physical Organic Chemistry of the Gas Phase. Reactivity Trends for Organic Cations;Topics in Current Chemistry;2003
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