Polar effects of 4‐substituents in the solvolysis of tetracyclo[6.2.1.1 3,6 .0 2,7 ]dodecan‐11‐yl triflates. Through‐space vs. inductive model
Author:
Affiliation:
1. Organisch‐Chemisches Institut der Technischen Universität München, Lichtenbergstraße 4, D‐8046 Garching
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19851180234
Reference37 articles.
1. The Electrostatic Influence of Substituents on the Dissociation Constants of Organic Acids. II
2. The origin of the inductive effect
3. Transmission of substituent effects. Generalization of the ellipsoidal cavity field effect model
4. Transmission of substituent effects. Dominance of field effects
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. σ-Assistance of the C4C7 bond in the solvolysis of 1-norbornyl triflates;Tetrahedron Letters;1994-03
2. Long range electrical field effects in solvolysis and13C-NMR shielding of androstanes with halogen, hydroxy and oxo substituents;Journal of Physical Organic Chemistry;1989-04
3. Solvolysis of 2-(2-methoxyethyl)-3-methyl-2-cyclohexenyl p-nitrobenzoate;Tetrahedron;1986-01
4. ChemInform Abstract: POLAR EFFECTS OF 4-SUBSTITUENTS IN THE SOLVOLYSIS OF TETRACYCLO(6.2.1.13,6.02,7)DODECAN-11-YL TRIFLATES. THROUGH-SPACE VS. INDUCTIVE MODEL;Chemischer Informationsdienst;1985-07-02
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