ChemInform Abstract: Synthesis of N6-Adenosine Adducts Expected from Cyclopenta-Ring Activation of Acenaphthylene and Aceanthrylene

Autor:	G. E. Toney, Avram Gold, L. J. Deterding, J. Charles, A. W. Bartczak, G. D. Marbury, Ramiah Sangaiah, D. J. Kelman
Rok vydání:	1990
Předmět:	Chemistry Stereochemistry Diastereomer General Medicine Ring (chemistry) Acenaphthylene Adenosine Adduct chemistry.chemical_compound Yield (chemistry) medicine Nucleoside Cis–trans isomerism medicine.drug
Zdroj:	ChemInform. 21
ISSN:	0931-7597
DOI:	10.1002/chin.199007319
Popis:	cis and trans Acenaphthen-1-amine-2-ol and trans aceanthren-1-amine-2-ol react with 2-chloropurine-9-β- D -ribofuranose to yield easily separable diastereomeric mixtures of N6-modified adenosine, corresponding to RNA adducts expected from the corresponding 1,2-oxides. These are the first examples of nucleoside adducts of cyclopentaPAH.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::7c38eb837dd082daf8a375ea0645000a https://doi.org/10.1002/chin.199007319 Zobrazit plný text záznamu Plný text