Abstract
The present work relates to the synthesis of pyrrolidine nucleoside analogs. Starting from malic acid, we have elaborated a high-yield synthesis of racemic and enantiomeric N-protected 3-pyrrolidinols and their O-mesyl derivatives as key compounds for alkylations of purine and pyrimidine nucleobases. On varying base and solvent, we have found conditions providing both satisfactory N-/O-regioisomeric ratio and acceptable yield for pyrimidine compounds.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antineoplastic Agents / pharmacology
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Antiviral Agents / pharmacology
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Chemistry, Pharmaceutical / methods
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Magnetic Resonance Spectroscopy
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Malates / chemistry
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Mass Spectrometry
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Models, Chemical
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Nucleic Acid Conformation
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Nucleosides / chemistry*
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Nucleotides / chemistry
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Purine Nucleosides / chemistry
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Purines / chemistry*
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Pyrimidine Nucleosides / chemistry
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Pyrimidines / chemistry*
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Solvents / chemistry
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Stereoisomerism
Substances
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Antineoplastic Agents
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Antiviral Agents
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Malates
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Nucleosides
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Nucleotides
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Purine Nucleosides
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Purines
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Pyrimidine Nucleosides
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Pyrimidines
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Solvents
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malic acid