PHOTODIMERIZATION KINETICS OF THYMINE-H2 AND THYMINE-D2
β Scribed by R. F. Borkman; B. S. Yamanashi
- Book ID
- 114891990
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 100 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0031-8655
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
1-(2-O-Acetyl-3,5,6-tri-O-benzoyl-beta-D-glucofuranosyl)thymine (1) was converted into the 2,2'-anhydro derivative 4 by selective deacetylation, mesylation, and treatment with 1,8-diazabicyclo[5.4.0]undec-7-ene. Cleavage of the 2,2'-anhydro ring in 4 with hydrogen bromide or hydrogen chloride led to
## Abstract The photodimerization reaction of pendant thymine bases in thymineβcontaining polyβlysine derivatives was studied over a wide range in aqueous solution. It was found that the quantum yield of the photodimerization of pendant thymine bases is affected mainly by the conformation of the po