The cope rearrangement in substituted semibullvalenes as studied by dynamic 13C NMR
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Barriers to thermally allowed reactions and the elusiveness of neutral homoaromaticity
2. Cope rearrangement revisited
3. 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 rearrangement
4. 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 semibullvalene
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1. Heavy‐Atom Tunneling in Semibullvalenes: How Driving Force, Substituents, and Environment Influence the Tunneling Rates;Chemistry – A European Journal;2020-07-28
2. An One-Pot Synthesis of Semibullvalenes and Its Mechanism;European Journal of Organic Chemistry;2002-03
3. The Effects of Substituents on the Degenerate Cope Rearrangement of Semibullvalenes and Barbaralanes;European Journal of Organic Chemistry;1998-10
4. The Search for Homoaromatic Semibullvalenes. 5.1 1,5-Dimethyl-2,4,6,8-semibullvalenetetracarboxylic Dianhydride;The Journal of Organic Chemistry;1998-04-18
5. Semibullvalenes—Homoaromatic bovines?;Advances in Theoretically Interesting Molecules;1998
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