Studies on the chemistry of 5-acetoxy-6-(acetoxymethyl)-uridines: Synthesis of a new type of 5'-cyclonucleoside Journal Article

  

Authors:	Sodum, R. S.; Otter, B. A.
Article Title:	Studies on the chemistry of 5-acetoxy-6-(acetoxymethyl)-uridines: Synthesis of a new type of 5'-cyclonucleoside
Abstract:	The 5-acetoxy-6-(acetoxymethyl)-nridine derivative 18 is converted in aqueous sodium hydroxide solution into the imidazole cyclonucleoside 22. Compound 22, in which an oxygen bridge links the sugar and base methano groups, represents a new type of 5'-cyclonucleoside. © 1986, Taylor & Francis Group, LLC. All rights reserved.
Keywords:	nonhuman; drug synthesis; nuclear magnetic resonance; theoretical study; drug identification; ultraviolet spectrophotometry; drug analysis; 2,3 dihydro 1 (2,3 o isopropylidene beta d ribofuranosyl) o5',2 methano 2 oxo 1h imidazole 4 carboxylic acid; 2,5' anhydro 5 hydroxy 2',3' o isopropylideneuridine
Journal Title:	Nucleosides & Nucleotides
Volume:	5
Issue:	4
ISSN:	0732-8311
Publisher:	Taylor & Francis Inc.
Date Published:	1986-01-01
Start Page:	385
End Page:	397
Language:	English
DOI:	10.1080/07328318608068680
PROVIDER:	scopus
DOI/URL:	https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023023413&doi=10.1080%2f07328318608068680&partnerID=40&md5=dd882c29ddf7794585338c1f4b763729
Notes:	Article -- Export Date: 18 August 2021 -- Source: Scopus

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