Stereoelectronic control of exo/endo rate ratios in the solvolysis of 2-norbornyl p-toluenesulfonates
- 31 December 1979
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 20 (21) , 1905-1908
- https://doi.org/10.1016/s0040-4039(01)86875-1
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Polar effects in the solvolysis of 6-exo-substituted endo-2-norbornyl p-toluenesulfonatesTetrahedron Letters, 1979
- Inductive, CC-hyperconjugative and frangomeric effects in the solvolysis of 6-exo-substituted 2-exo-norbornyl p-toluenesulfonatesTetrahedron Letters, 1979
- Inductive, Hyperconjugative and Frangomeric Effects in the Solvolysis of 1‐Substituted 3‐Bromoadamantanes. Polar effects IVHelvetica Chimica Acta, 1978
- Polar Effects in Organic ReactionsAngewandte Chemie International Edition in English, 1976
- The Derivation of Inductive Substituent Constants from pKa Values of 4‐Substituted Quinuclidines. Polar effects. Part IHelvetica Chimica Acta, 1976
- Nucleophilic Reactions at Tertiary Carbon. Part 1. The 1,2‐dimethyl‐1‐cyclohexyl cationHelvetica Chimica Acta, 1973
- Nucleophilic Reactions at Tertiary Carbon. Part 3. σ‐ and π‐routes to the 9‐decalyl cationHelvetica Chimica Acta, 1973
- Nucleophilic Reactions at Tertiary Carbon. Part 2. σ‐ and π‐routes to the 8‐hydrindanyl cationHelvetica Chimica Acta, 1973
- Neighboring Carbon and Hydrogen. XI. Solvolysis of exo-Norbornyl p-Bromobenzenesulfonate1,2,3Journal of the American Chemical Society, 1952
- Neighboring Carbon and Hydrogen. X. Solvolysis of endo-Norbornyl Arylsulfonates1,2,3Journal of the American Chemical Society, 1952