In continuation of our studies of sterically crowded, acyclic hydrocarbons with hindered rotation about carbon-carbon single bondsI, we have prepared tetraisopropylethylene, BL, and its tetradeuterio 2 analogue, lb, by the reductive coupling reaction of McMurry and Fleming, reaction 1. Compound&, wh
Sterically hindered internal rotation in acyclic hydrocarbons: 2,5-dimethyl-3,4-diisopropyl-2,4hexadiene
β Scribed by David S. Bomse; Thomas Hellman Morton
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- French
- Weight
- 229 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Hindered rotation about single bonds baa been observed in a wide variety of molecules. Recent investigations of substituted butadienes have used nmr techniques to characterize this phenomenon, which renders these molecnles cbirall.
We wish to report the preparation of hydrocarbons~and~, substituted dienes that exhibit unusually high barriers to rotation about carbon-carbon single bonds.
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