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Synthesis of novel isoxazolinyl substituted imidazo[1,2-a]pyridine C-nucleoside analogs

✍ Scribed by Shifeng Pan; Guoping Wang; Raymond F. Schinazi; Kang Zhao


Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
243 KB
Volume
39
Category
Article
ISSN
0040-4039

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✦ Synopsis


carbon-carbon bonds for the synthesis of new C-nucleoside analogs 7 and 8. These two isomers, possessing altered positions of nitrogen and oxygen atoms, can be formed through dipolar cycloaddition reactions of the appropriate olefms and nitrile oxides.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Synthesis of Novel
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Synthesis of Novel Isoxazolinyl Substituted Imidazo[1,2-a]pyridine C-Nucleoside Analogues. -The title isomeric C-nucleoside analogues (VI) and (IX) having hydroxymethyl-substituted isoxazoline rings in place of the ribose ring are prepared by a strategy involving cycloaddition of olefins to interme

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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 β€œFull Text” option. The original article is trackable v