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 observ
✦ LIBER ✦
Reaction of nucleobases with α-acetylenic esters, potentially useful for chemical modification of nucleic acids
✍ Scribed by M. Olomucki; J.Y. Le Gall; S. Colinart; F. Durant; B. Norberg; G. Evrard
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- French
- Weight
- 252 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
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 conditions with nucleophiles analogous to those present in proteins2. Tests with small model molecules and with proteins
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