Enamine-singlet oxygen reactions. α-Diketones from intermediate amino dioxetanes
- 31 December 1975
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 16 (21) , 1735-1738
- https://doi.org/10.1016/s0040-4039(00)72246-5
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Photosensitized oxidation of an enaminoketone. Total synthesis of a rhoeadine alkaloidJournal of the American Chemical Society, 1974
- Chemistry of singlet oxygen. IX. Stable dioxetane from photooxygenation of tetramethoxyethyleneJournal of the American Chemical Society, 1970
- Stereospecific formation of 1,2-dioxetanes from cis- and trans-diethoxyethylenes by singlet oxygenJournal of the American Chemical Society, 1970
- Photo-induced reactions. XV. The nature of peroxide intermediates in the photosensitized oxygenation of purine derivativesTetrahedron Letters, 1968
- Photooxygenation of enamines - a partial synthesis of progesteroneTetrahedron Letters, 1968
- Chemistry of singlet oxygen. VI. Photooxygenation of enamines: evidence for an intermediateTetrahedron Letters, 1968
- Autoxidation of enamines and Schiff bases of .alpha.,.beta.-unsaturated ketones. A new synthesis of unsaturated 1,4-dionesJournal of the American Chemical Society, 1968
- The reactions of heterocyclic systems with singlet oxygen. Photosensitized oxygenation of imidazolesTetrahedron Letters, 1968
- Studies in Organic Sulfur Compounds. XI.1 On the Reaction of Enamines with Hydrogen Sulfide2The Journal of Organic Chemistry, 1962
- Internal Rotation. VI. A Dilute Solution Method for the Spectroscopic Determination of the Energy Difference between Rotational Isomers1Journal of the American Chemical Society, 1951