Abstract
Photolysis of the title, compounds results in efficient hydrogen transfer reaction to produce 1.5-biradical intermediate, which does not form in the photolysis of a structurally similar compound, α- (otolyl)isobutyroplienone. From their kinetic studies we have measured the rearrangement rate constant of a substituted oxiranylcarbinyl radical.
| Original language | English |
|---|---|
| Pages (from-to) | 903-906 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 40 |
| Issue number | 5 |
| DOIs | |
| State | Published - 29 Jan 1999 |
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Dive into the research topics of 'Photochemistry of 1-(o-Tolyl)-1-benzoylcyclopropane and 2-(o-tolyl)-2- benzoyloxirane: Determination of ring opening rates of oxiranylcarbinyl radicals'. Together they form a unique fingerprint.Cite this
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