The structure of the radical reaction product between thiamine and 4-0x0-2,2,6,6tetramethylpiperidine-1-oxyl has been investigated by X-ray crystallographic analysis. This structure had already been proposed by means of Mass-spectrometry and various chemical reactions. 1) CL3
N6-Hydroxy-2-aminopurine, N4-hydroxycytidine and 5-methyl-N4-hydroxideoxycytidine: potent mutagens of the base analog type
β Scribed by Celina Janion
- Book ID
- 113248972
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- English
- Weight
- 147 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0165-1161
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π SIMILAR VOLUMES
Methyl 3,4-diphenyl-5-hydroxylamino-2-furoate (N-OH-MDPF) (I), methyl 3,4-diphenyl-5-acetoxyamino-2-furoate (N-OAc-MDPF) (II), methyl 3,4-diphenyl-N-hydroxy-5-acetylamino-2-furoate (N-OH-MDPAF) (III), and methyl 3,4-diphenyl-N-acetoxy-5-acetylamino-2-furoate (N-OAc-MDPAF) (IV) were synthesized and t
## Abstract Infrared spectroscopy has been employed to study possible base pair interactions, in nonpolar media, between O^6^βmethylguanine and uracil, cytosine and adenine; and between derivatives of N^4^βhydroxycytosine and adenine. The association constants of O^6^βmethylguanine with uracil, cyt
## Abstract For Abstract see ChemInform Abstract in Full Text.