Norbornanes. Part 19. The Inductive Model for Norbornyl Cation Formation
Author:
Publisher
Wiley
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis
Reference30 articles.
1. Carbon Participation in the Solvolysis of 6-exo-substituted 2-exo- and 2-endo-Norbornylp-Toluenesulfonates. Norbornanes part 5
2. Carbon Participation in the Solvolysis of 6- and 7-Substituted 2-Norbornylp-Toluenesulfonates. Norbornanes, Part 11
3. Norbornanes. Part 10. Solvolysis of the Stereoisomeric 6-Cyano-2-norbornylp-Toluenesulfonates. A Correction
4. Norbornanes. Part 18. Inductive Charge Dispersal in the Solvolyses of 4- and 5-Substituted 2-Norbornylp-Toluenesulfonates
5. A Reexamination of Inductive Substituent Constants Derived from pKa Values of 4-Substituted Quinuclidines. Polar effects. Part VIII
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1. 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
2. Nature of the Electronic Factor Governing Diastereofacial Selectivity in Some Reactions of Rigid Saturated Model Substrates;Chemical Reviews;1999-04-07
3. Rearrangements of Spirocyclobutane-Substituted 2-Norbornyl Cations;European Journal of Organic Chemistry;1998-02
4. Why the Classical and Nonclassical Norbornyl Cations Do Not Resemble the 2-endo- and 2-exo-Norbornyl Solvolysis Transition States1,;The Journal of Organic Chemistry;1997-06-01
5. Deamination Reactions, 56. Cyclopropane Participation in Norbornyl Cations;Liebigs Annalen;1995-04
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