The cope rearrangement in substituted semibullvalenes as studied by dynamic 13C NMR
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (7) , 749-752
- https://doi.org/10.1016/s0040-4039(01)80016-2
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Intramoleculare (4+2)-cycloadditionen mit inversem elektronenbedarfTetrahedron Letters, 1983
- 2, 6-dicyan-1, 5-dimethyl-semibullvalenTetrahedron Letters, 1982
- A 2,6‐DiazasemibullvaleneAngewandte Chemie International Edition in English, 1982
- Semibullvalenetetracarboxylates: Models for Molecules with Bishomoaromatic Ground StateAngewandte Chemie International Edition in English, 1982
- 2,6-dicyano-1,5-dimethylsemibullvalene as a probe for homoaromatic molecules of the Dewar-Hoffman typeTetrahedron Letters, 1982
- Semibullvalenes. 1. Synthesis and crystal structure of 1,5-dimethyl-2,4,6,8-tetrakis(carbomethoxy)tricyclo[3.3.0.02,8]octa-3,6-diene a donor-acceptor-substituted semibullvaleneJournal of the American Chemical Society, 1981
- One-Pot Synthesis of Substituted SemibullvalenesAngewandte Chemie International Edition in English, 1980
- Barriers to thermally allowed reactions and the elusiveness of neutral homoaromaticityJournal of the American Chemical Society, 1979
- Cope rearrangement revisitedJournal of the American Chemical Society, 1971
- Ground states of .sigma.-bonded molecules. XIV. Application of energy partitioning to the MINDO [modified intermediate neglect of differential overlap] /2 method and a study of the Cope rearrangementJournal of the American Chemical Society, 1971