Synthesis of Ribo‐Azanucleosides by Anodic Oxidation: Reactivity Control of Intermediate for Efficient Access to Pharmacophores-Reference-Cited by-同舟云学术

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Synthesis of Ribo‐Azanucleosides by Anodic Oxidation: Reactivity Control of Intermediate for Efficient Access to Pharmacophores

Published:2018-11-05 Issue:68 Volume:24 Page:17902-17905
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Okamoto Kazuhiro¹,Shoji Takao¹,Tsutsui Mizuki¹,Shida Naoki¹,Chiba Kazuhiro¹^ORCID

Affiliation:

1. Department of Applied Biological ScienceTokyo University of Agriculture and Technology 3-5-8 Saiwai-cho, Fuchu Tokyo 183-8509 Japan

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201804285

Reference29 articles.

1.

2. Chemical Synthesis of Heterocyclic−Sugar Nucleoside Analogues

3. Nucleoside Analogues: Synthesis and Biological Properties of Azanucleoside Derivatives

4.

5. Stereoselective Synthesis and Biological Evaluations of Novel 3′-Deoxy-4′-azaribonucleosides as Inhibitors of Hepatitis C Virus RNA Replication

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5. Stereoselective Production of Imino‐ d ‐ribitol and C ‐Azanucleosides through Electrochemical C−H Functionalization;European Journal of Organic Chemistry;2022-11-21

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