Nucleic acid components and their analogues: A novel and efficient method for the synthesis of a new class of bipyridyl and biheterocyclic-nitrogen thioglycosides from pyridine-2(1H)-thiones

A novel synthesis of a new class of bipyridyl and biheterocyclic-nitrogen thioglycosides utilizing the reactions of heterocyclic substituted pyridine-2(1H)-thiones and alpha-bromoglucose or alpha-bromogalactose tetraacetate as starting components is described.

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Bibliographic Details
Published inNucleosides, nucleotides & nucleic acids Vol. 21; no. 6-7; pp. 477 - 493
Main Authors Elgemeie, GH, El-Enany, MM, Ismail, MM, Ahmed, EK
Format Journal Article
LanguageEnglish
Published PHILADELPHIA Taylor & Francis 01.06.2002
Subjects
2,2'-Dipyridyl - chemical synthesis
2,2'-Dipyridyl - chemistry
Biochemistry & Molecular Biology
Cycloparaffins - chemistry
Galactose - chemistry
Glucose - chemistry
Heterocyclic Compounds - chemical synthesis
Heterocyclic Compounds - chemistry
Life Sciences & Biomedicine
Magnetic Resonance Spectroscopy
Nitriles - chemistry
Nitrogen - chemistry
Science & Technology
Thioglycosides - chemical synthesis
Thiones - chemistry
biheterocyclic thioglycosides
pyridine-2(1H)-thiones
NUCLEOSIDES
pyridine thioglycosides
coupling reactions
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Summary:A novel synthesis of a new class of bipyridyl and biheterocyclic-nitrogen thioglycosides utilizing the reactions of heterocyclic substituted pyridine-2(1H)-thiones and alpha-bromoglucose or alpha-bromogalactose tetraacetate as starting components is described.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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ISSN:1525-7770
1532-2335
DOI:10.1081/NCN-120014820