A new approach to the synthesis of nucleoside analogs has been developed, which involves initial chemo-and regioselective cohalogenation of 1-N-vinylpyrimidinediones 10a,b using N-bromosuccinimide in the presence of variously substituted propargylic alcohols. Radical carbocyclization of the resultin
β¦ LIBER β¦
ChemInform Abstract: The Cohalogenation of 1-N-Vinylpyrimidinediones: A New Approach to Nucleoside Analogues.
β Scribed by Nathalie Baret; Jean-Pierre Dulcere; Jean Rodriguez; Jean-Marc Pons; Robert Faure
- Publisher
- John Wiley and Sons
- Year
- 2001
- Weight
- 34 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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## 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
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