Smooth and selective formation of the cyclic 1,N2-propano adducts in the reactions of guanine nucleosides and nucleotides with acetaldehyde
โ Scribed by Magoichi Sako; Isamu Yaekura; Yoshihiro Deyashiki
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 71 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
The treatment of guanine nucleosides and nucleotides with excess acetaldehyde in pH 8.0 phosphate buffer containing a basic amino acid such as arginine and lysine resulted in the smooth and selective formation of the corresponding cyclic 1,N 2 -propano adducts even under mild conditions.
๐ SIMILAR VOLUMES
Dynamics of ternary complex formation in the reaction of diaquoanthranilato-N , Ndiacetatonickelate(l1) with 2,2'-bipyridine and I ,lo-phenanthroline. Ni(adal( H2012- ## and L = bipy or phen The kinetics of formation of ternary complexes by diaquoanthranilato-N, Ndtacetatonickelate[ i l ) , [Nl(a