The NH2 group and the adjacent ring nitrogen of adenosine and cytidine react with a-acetylenic esters by addition across the triple bond and formation of a lactam with the ester group. We have recently shown that chlorotetrolic (4-chloro-2-butynoic) esters', C1CH2-CzC-COOR, react under mild conditi
New reaction of adenine and cytosine derivatives, potentially useful for nucleic acids modification.
β Scribed by N.K. Kochetkov; V.N. Shibaev; A.A. Kost
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- French
- Weight
- 202 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The chemical modification of the base residues in nucleic acids is of importance for structural and functional investigation of RNA and DNA /I/.
A search of new specific chemical reactions for this purpose seems to be essential for the future development of this field.
We wish to report our observations about interaction of chloroacetaldehyde with nucleic acid components. This reaction may form a basis for the new method of nucleic acid modification. We have found that chloroacetaldehyde reacts readily with 9-N-methyladenine and I-N-methylcytosine in weakly acidic aqueous solutions (in former case , addition of ethanol is necessary for homogeneity of the reaction mixture)to give 3-methylimidazo/2,1-i/purinetAj from 9-N-methyladenine.
COCw,CHO
The analytical sample of p&chlorate of Ahas m.p. 295-6Β°(decomp.).
π SIMILAR VOLUMES