Abstract
Relative kinetic acidity measurements have shown that the cyclobutyl group has the ability to stabilize an adjacent carbanion center similar to vinyl and cyclopropyl groups, although to a lesser extent. The results of semiempirical calculations (MNDO) covering all the mentioned substituents, including the isopropyl group correlate well with the experimentally determined relative kinetic acidities.
| Original language | English |
|---|---|
| Pages (from-to) | 139-142 |
| Number of pages | 4 |
| Journal | Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics |
| Volume | 96 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 1992 |
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