Photosensitized dimerization of methylcytosine derivatives
โ Scribed by Taguchi, Hiroyasu; Hahn, Bo-Sup; Wang, Shih Y.
- Book ID
- 126041041
- Publisher
- American Chemical Society
- Year
- 1977
- Tongue
- English
- Weight
- 635 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Since thymine dimerization is the main photochemical lesion occuring in uv irradiated DNA, an understanding of the mechanism of dimerization is biologically significant. Both photosensitized and direct dimerization are important in DNA, but because photosensitized thymine dimerization has been less
There have been two recent reports on the photodirerization of substituted cyclopropenes. A. R. Stechl has found' that 1,3,3-trimethylcyclopropene, on irradiation in the presence of benzophenone , produces two isoneric dimers, both tricyclo\_~,1,0,02~47-hexane derivatives. Obata and Moritani' report