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Sterically hindered internal rotation in acyclic hydrocarbons: 2,5-dimethyl-3,4-diisopropyl-2,4hexadiene

✍ 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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✦ 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.


πŸ“œ SIMILAR VOLUMES


Sterically hindered internal rotation in
✍ David S. Bomse; Thomas Hellman Morton πŸ“‚ Article πŸ“… 1975 πŸ› Elsevier Science 🌐 French βš– 216 KB

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

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v