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Synthesis of Imidazo[1,2- a ]pyridine C-Nucleosides with an Unexpected Site of Ribosylation

✍ Scribed by Gudmundsson, Kristjan S.; Drach, John C.; Townsend, Leroy B.

Book ID: 120369907
Publisher: American Chemical Society
Year: 1997
Tongue: English
Weight: 293 KB
Volume: 62
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo9619342

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ChemInform Abstract: Synthesis of Imidaz

ChemInform Abstract: Synthesis of Imidazo(1,2-a)pyridine C-Nucleosides with an Unexpected Site of Ribosylation.

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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

The condensation of 2,6-dichloroimidazo[

The condensation of 2,6-dichloroimidazo[1,2-a]pyridine with ribonolactone gives a novel imidazo[1,2-a]pyridine C-nucleoside with an unexpected site of ribosylation

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ChemInform Abstract: The Condensation of

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Synthesis of the First C3 Ribosylated Im

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Synthesis of novel isoxazolinyl substitu

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

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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.

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ChemInform Abstract: Synthesis of Novel Isoxazolinyl Substituted Imidazo[1,2-a]pyridine C-Nucleoside Analogues.

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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