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Singlet and triplet states in cycloaddition to conjugated dienes
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Paul D. Bartlett
Veröffentlicht/Copyright:
1. Januar 2009
Published Online: 2009-01-01
Published in Print: 1968-01-01
© 2013 Walter de Gruyter GmbH, Berlin/Boston
Artikel in diesem Heft
- Preface
- The use of photochemical reactions in organic synthesis
- Photochemical reactions with non-conjugated dienes
- Photoaddition and photoisomerization reactions of the benzene ring
- Mercury (3P1) sensitized photoreactions of furan: Details of the primary processes
- Cyclic ketones: Photolytic eliminations and reductions
- Photosensitized isomerizations of dideuteroethylenes
- Photochemistry of cyclic ketones in solution
- Electron-transfer and complex formation in the excited state
- Fate of the excitation energy in the quenching of fluorescence by conjugated dienes
- Some problems in aromatic photosubstitution
- Mechanism of the Tübingen photooximation reaction
- Photooxydation des dérivés aromatiques
- Singlet and triplet states in cycloaddition to conjugated dienes
Artikel in diesem Heft
- Preface
- The use of photochemical reactions in organic synthesis
- Photochemical reactions with non-conjugated dienes
- Photoaddition and photoisomerization reactions of the benzene ring
- Mercury (3P1) sensitized photoreactions of furan: Details of the primary processes
- Cyclic ketones: Photolytic eliminations and reductions
- Photosensitized isomerizations of dideuteroethylenes
- Photochemistry of cyclic ketones in solution
- Electron-transfer and complex formation in the excited state
- Fate of the excitation energy in the quenching of fluorescence by conjugated dienes
- Some problems in aromatic photosubstitution
- Mechanism of the Tübingen photooximation reaction
- Photooxydation des dérivés aromatiques
- Singlet and triplet states in cycloaddition to conjugated dienes