| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277955 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
A new type of ring-chain tautomerism, which consists of the reversible conversion of bicyclo[4.2.0]octane derivatives into trisubstituted enamines was found and studied by 1H NMR spectroscopy. The starting materials were prepared by the stereoselective reaction of (E)-3,3,3-trichloro-1-nitropropene with cyclohexanone enamines.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
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Authors
Vladislav Yu. Korotaev, Alexey Yu. Barkov, Pavel A. Slepukhin, Mikhail I. Kodess, Vyacheslav Ya. Sosnovskikh,