Superelectrophilic Protio Methyl- and Protio Dimethylmethyleniminium Dications1
Author:
Affiliation:
1. Loker Hydrocarbon Research Institute and Department of Chemistry, University of Southern California, University Park, Los Angeles, California 90089-1661
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo020351r
Reference22 articles.
1. Structures and stabilities of higher coordinate onium-boronium dications (X+BH3+ and X+BH5+; X = NH3, PH3, H2O, and H2S)
2. Carcinogen chemistry. 2. Carbon-13 nuclear magnetic resonance spectroscopic study of the ambident carbocationic nature of iminium ions and its relevance to the aminoalkylating ability of related chemical carcinogens
3. Superelectrophiles
4. Structure and energies of CH2X+ (XNH2, PH2, OH, SH, F and Cl) cations and their protonated CH2XH2+ and CH3X2+ dications
5. Experimental and theoretical studies on the charge stripping from CH3X+ and CH2XH+? ions (X = F, Cl, Br, I, OH, SH, or NH2)
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1. Electrophilicity Scales for Carbocations;Carbocation Chemistry;2014-08-15
2. Recent studies of persistent carbodications;Advances in Physical Organic Chemistry;2009
3. The influence of electronegativity on triangular three-centre two-electron bonds: the relative stability of carbonium ions, π-complex chemistry and the −2hβ effect;Tetrahedron;2004-03
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