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Journals / Turkish Journal of Chemistry / 2002 / Cilt: 26 - Sayı: 2

Synthesis of 2'-deoxy-2'-fluoro-L-arabinofuranosyl imidazole derivatives

Süreyya ÖLGEN
Pages
255–261
Publication Date
2022-11-04
DOI
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⚡ TL;DR(Too Long; Didn't Read)

The characterization of the compounds was accomplished by elemental analysis, $^1H$-NMR, $^{13}C$-NMR, IR, UV-VIS spectral data and optical rotation.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:A new series of imidazole nucleosides was synthesized via direct condensation and construction of heterocyclic moiety from glycosyl amine templates.
📊
Key Findings & Data:A new series of imidazole nucleosides was synthesized via direct condensation and construction of heterocyclic moiety from glycosyl amine templates.
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Conclusion & Impact:The characterization of the compounds was accomplished by elemental analysis, $^1H$-NMR, $^{13}C$-NMR, IR, UV-VIS spectral data and optical rotation.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

A new series of imidazole nucleosides was synthesized via direct condensation and construction of heterocyclic moiety from glycosyl amine templates. The characterization of the compounds was accomplished by elemental analysis, $^1H$-NMR, $^{13}C$-NMR, IR, UV-VIS spectral data and optical rotation.

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Cite This Article

ÖLGEN, S. (2022). Synthesis of 2'-deoxy-2'-fluoro-L-arabinofuranosyl imidazole derivatives. Turkish Journal of Chemistry, Cilt: 26 - Sayı: 2, 255–261. https://ajindex.com/articles/602301

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