Photolysis of Oacyl-N-hydroxy-2-thiopyridone, derived from 2-tetrahydrofuryl carboxylic acid or 2,5anhydro-D-allonic acid, gave the corresponding Gnucleoside derivatives in the presence of heteroaromatic compounds via radical pathways.
Synthesis of nucleoside derivatives via heterocyclocondensation reactions
β Scribed by Vincent Kikelj; Paul Setzer; Karine Julienne; Jean-Claude Meslin; David Deniaud
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- French
- Weight
- 111 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
A new synthesis of nucleoside analogues has been developed. The cyclocondensation of a glycosylated diazadiene or thiazadiene, with acyl chlorides or a-halogenoketones, respectively, resulted in good yields and excellent regioselectivities. We report an efficient method for the production of glucosyl pyrimidinones and glucosylamino thiazoles.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v