Issue 0, 1971

Synthetic analogues of polynucleotides. Part VII. Further syntheses of 5′-O-acryloylnucleosides and copolymers of these with other acryloyl compounds

Abstract

The synthesis of the 5′-O-acryloyl esters of cytidine, guanosine, and adenosine, by the action of acrylic anhydride on suitably protected nucleosides, followed by removal of the protecting groups, is described. These esters have been copolymerised with acrylamide to give water-soluble copolymers. Copolymers of 5′-O-acryloylcytidine with 6-O-acryloylgalactose have also been prepared.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 3183-3187

Synthetic analogues of polynucleotides. Part VII. Further syntheses of 5′-O-acryloylnucleosides and copolymers of these with other acryloyl compounds

M. J. Cooper, R. S. Goody, A. S. Jones, J. R. Tittensor and R. T. Walker, J. Chem. Soc. C, 1971, 3183 DOI: 10.1039/J39710003183

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements