A Photoallylation of N-Methylarenedicarboximides by Allylsilanes
- 5 October 1986
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 15 (10) , 1749-1752
- https://doi.org/10.1246/cl.1986.1749
Abstract
The photoallylation of N-methylarenedicarboximides by allylsilanes in acetonitrile or methanol efficiently occurred at a carbonyl carbon atom and at an aromatic carbon atom possibly via single electron transfer.This publication has 6 references indexed in Scilit:
- Photoinduced methanol-incorporated cyclization of N-(3-phenylallyl)arenedicarboximidesThe Journal of Organic Chemistry, 1985
- Photoreduction of N-methylphthalimide with 2,3-dimethyl-2-butene. Evidence for reaction through an electron transfer generated ion pairJournal of the American Chemical Society, 1984
- Exploratory and mechanistic studies of the electron-transfer-initiated photoaddition reactions of allylsilane-iminium salt systemsThe Journal of Organic Chemistry, 1984
- Electron-transfer initiated photoaddition of allylsilanes to 1-methyl-2-phenylpyrrolinium perchlorate. A novel allylation methodologyJournal of the American Chemical Society, 1982
- Solvent-incorporated medium to macrocyclic compounds by the photochemical cyclization of N-alkenylphthalimidesJournal of the American Chemical Society, 1978
- Kinetics of Fluorescence Quenching by Electron and H‐Atom TransferIsrael Journal of Chemistry, 1970