Die photosensibilisierte oxydation semicyclischer doppelbindungen
E Klein, W Rojahn
Index: Klein,E.; Rojahn,W. Tetrahedron, 1965 , vol. 21, p. 2173 - 2178
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Citation Number: 18
Abstract
The photosensitized oxygenation of semicyclic double bonds is highly sterically controlled. Little changes in the geometry of the ring system have a considerable influence on the direction of the reaction. This is demonstrated by the results of this reaction with methylencyclopentane, methylencyclohexane, methylencycloheptane, Δ1 (7)-p-menthene, Δ4 (8)-p-menthene, terpinolene and Δ2, 4 (8)-p-mentha-diene.
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