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Alkylation and Convalent Adduct Formation of 2-Oxopurine
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry, Organic Chemistry.
Department of Chemistry, University of Oslo.
Department of Chemistry, University of Oslo.
1993 (English)In: Heterocycles, ISSN 0385-5414, E-ISSN 1881-0942, Vol. 36, no 2, 231-235 p.Article in journal (Refereed) Published
Abstract [en]

2-Oxopurine reacted with benzyl bromide and ethanol to give the covalent adduct 1,3,7-tribenzyl-6-ethoxy-2-oxopurine, as well as dibenzylated products. Carbon-carbon bond formation was observed in the reaction between 2-oxopurine, dry silica gel, and benzyl bromide, giving rise to 6-hydroxy-1,3,8-tribenzyl-2-oxopurine.

Place, publisher, year, edition, pages
1993. Vol. 36, no 2, 231-235 p.
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Natural Sciences
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URN: urn:nbn:se:uu:diva-140713DOI: 10.3987/COM-92-6201OAI: oai:DiVA.org:uu-140713DiVA: diva2:384251
Available from: 2011-01-08 Created: 2011-01-08 Last updated: 2017-12-11Bibliographically approved

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Gogoll, Adolf

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