Synthesis of 8-alkoxy-6-alkylamino-2-alkylthiopurine nucleosides with a straightforward multiple-functionalization strategy-Reference-Cited by-同舟云学术

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Synthesis of 8-alkoxy-6-alkylamino-2-alkylthiopurine nucleosides with a straightforward multiple-functionalization strategy

Published:2016-07 Issue:27-28 Volume:57 Page:2949-2953
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Du Hongguang,Sun Xiaoyang,Yu Mingwu,Tian Miao,Li Shunlai,Wang Zhiqian

Funder

National Natural Science Foundation of China

Fundamental Research Funds

Public Hatching Platform for Recruited Talents of Beijing University of Chemical Technology

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. Nucleosides and nucleotides. 103. 2-Alkynyladenosines: a novel class of selective adenosine A2 receptor agonists with potent antihypertensive effects

2. (N)-Methanocarba 2,N6-Disubstituted Adenine Nucleosides as Highly Potent and Selective A3 Adenosine Receptor Agonists

3. Design, Synthesis, and Antiviral Activity of Adenosine 5‘-Phosphonate Analogues as Chain Terminators against Hepatitis C Virus

4. Adenosine Kinase Inhibitors. 4. 6,8-Disubstituted Purine Nucleoside Derivatives. Synthesis, Conformation, and Enzyme Inhibition

5. Inhibition of Nucleoside Transport Proteins by C8-Alkylamine-Substituted Purines

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1. Visible Light‐Mediated Late‐Stage Thioetherification of Mercaptopurine Derivatives;Chemistry – A European Journal;2024-08-07

2. One-Step Visible Light Photoredox-Catalyzed Purine C8 Alkoxylation with Alcohol;The Journal of Organic Chemistry;2022-08-19

3. Palladium‐Catalyzed N ³ ‐Directed C−H Halogenation of N ⁹ ‐Arylpurines and Azapurines;European Journal of Organic Chemistry;2022-02-21

4. Application of diazonium chemistry in purine modifications: A focused review;Journal of Heterocyclic Chemistry;2021-08-09

5. Synthetic developments on the preparation of sulfides from thiol-free reagents;Organic Chemistry Frontiers;2021

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