Syntheses of Anomeric Pairs of New C-Nucleosides via 1,3-Dipolar Cycloaddition Reaction. Part 1. -The vicinal hydroxy groups of D-ribose (I) are protected by a modified method which shows advantages over the prevailing literature procedure and leads to anomerically pure isopropylidene derivative (I
ChemInform Abstract: Access to a New Type of Homo-C-Nucleosides with a “Split” 8- Deazapurine via a 1,3-Dipolar Cycloaddition Reaction.
✍ Scribed by S. VAN CALENBERGH; A. DE BRUYN; J. SCHRAML; N. BLATON; O. PEETERS; D. DE KEUKELEIRE; R. BUSSON; P. HERDEWIJN
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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The Synthesis of a New Pyrazolylimidazolinone via 1,3-Dipolar Cycloaddition Reaction of N-Methylsydnone with Methyl Propiolate. -A facile and new procedure for the synthesis of the title compound (IX), a compound with potential herbicidal activity, involving the thermally induced 1,3-dipolar cycloa
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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 “Full Text” option. The original article is trackable v