Photochemically Initiated, Electron‐Transfer‐Catalyzed Diels‐Alder Reactions of Electron‐Rich Dienophiles
- 1 May 1985
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 24 (5) , 412-414
- https://doi.org/10.1002/anie.198504121
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Cation radical Diels-Alder reactions of electron-rich dienophilesJournal of the American Chemical Society, 1983
- Cation radical catalyzed olefin cyclodimerizationJournal of the American Chemical Society, 1983
- Photosensitized [4 + 2] cyclodimerization of 1,3-cyclohexadieneJournal of the American Chemical Society, 1983
- Selectivity profile of the cation radical Diels-Alder reactionJournal of the American Chemical Society, 1982
- Photocycloreversion-reaction of a cage molecule and related cyclobutanes with cationic sensitizersTetrahedron Letters, 1981
- Oxygenation reactions of the adamantylideneadamantane cation radicalJournal of the American Chemical Society, 1981
- Cation-radical catalyzed Diels-Alder reactionJournal of the American Chemical Society, 1981
- Mechanisms of photooxygenation. 2. Formation of 1,2-dioxetanes via 9,10-dicyanoanthracene-sensitized electron-transfer processesJournal of the American Chemical Society, 1980
- Methods of Reactivity UmpolungAngewandte Chemie International Edition in English, 1979
- Methoden der ReaktivitätsumpolungAngewandte Chemie, 1979