Anthraquinone derivatives as sensitizers of the formation of singlet oxygen
β Scribed by I. M. Byteva; G. P. Gurinovich; O. L. Golomb; V. V. Karpov
- Publisher
- Springer US
- Year
- 1986
- Tongue
- English
- Weight
- 235 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0021-9037
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The ten-butyl ester of 3-methoxy-2-pyrrolecarboxylic acid 3 undergoes reaction with singlet oxygen to form an intermediate imino hydroperoxide 4. This hydroperoxide may be trapped by a variety of nucleophiles yielding 5substituted pyrroles 6. With strong nucleophilic substituents at the 5-position,
Study of the photochemical coupling reaction between 2-iodo-5-nitrothiophene and indolyl derivatives indicated that the coupling reaction occurs on the C-2 position of indole to give products showing absorptions in the visible region. The photochemical reaction between iodoheterocyclic derivatives a