Unexpected influence of mono-phenyl substitution on the photochemistry of β,γ-unsaturated oxime acetates
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1990/C3/C39900000934
Reference5 articles.
1. The photochemical synthesis of potential pyrethroid components by the aza-di-π-methane rearrangement of β,γ-unsaturated oxime acetates.
2. Photochemistry of acyclic β,γ-unsaturated ketones. The effect of substituents at the α-C and the carbonyl group on the occurrence of the oxa-di-π-methane rearrangement
3. Di-.pi.-methane and oxa-di-.pi.-methane rearrangements
4. Photochemistry of β, γ-unsaturated ketones-V
5. Mechanistic and exploratory organic photochemistry. XLI. Di-.pi.-methane rearrangement. Interaction of electronically excited vinyl chromophores
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5. Photochemical Reactivity of 1-Substituted-1-aza-1,4-dienes Promoted by Electron-Acceptor Sensitizers. Di-π-methane Rearrangements and Alternative Reactions via Radical-Cation Intermediates;The Journal of Organic Chemistry;2002-11-23
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