Pyrazolo[1,5-a]-1,3,5-triazine C-Nucleoside as Deoxyadenosine Analogue: Synthesis, Pairing, and Resistance to Hydrolysis-Reference-Cited by-同舟云学术

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Pyrazolo[1,5-a]-1,3,5-triazine C-Nucleoside as Deoxyadenosine Analogue: Synthesis, Pairing, and Resistance to Hydrolysis

Published:2014-03-20 Issue:7 Volume:79 Page:3221-3227
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lefoix Myriam¹,Mathis Gérald¹,Kleinmann Tirtsa²,Truffert Jean-Christophe¹,Asseline Ulysse³

Affiliation:

1. NucleoSyn. Pépinières d’entreprises - Centre Innovation 16, Rue Léonard de Vinci 45074 Orléans Cedex 2, France

2. Bio-Lab Limited, POB 34038 Jerusalem, Israel

3. Centre de Biophysique Moléculaire UPR 4301 CNRS, Conventionnée avec l’Université d’Orléans, Rue Charles Sadron, 45071 Orléans Cedex 02, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo5000253

Reference49 articles.

1. Fluorescence based strategies for genetic analysis

2. MicroRNA Profiling Can Classify Acute Leukemias of Ambiguous Lineage as Either Acute Myeloid Leukemia or Acute Lymphoid Leukemia

3. Aptamer Modules as Sensors and Detectors

4. Four-Color, Enzyme-Free Interrogation of DNA Sequences with Chemically Activated, 3′-Fluorophore-Labeled Nucleotides

5. Synthesis and Characterization of Oligodeoxynucleotides Containing Formamidopyrimidine Lesions and Nonhydrolyzable Analogues

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1. Unexpected transformations of 3-bromo-5,7-dimethylpyrazolo[1,5-a]pyrimidine in reactions with BunLi;Russian Chemical Bulletin;2024-06

2. Synthesis and Properties of 2′-Deoxyadenosine Mimics Bearing a Thieno[3,2-d]pyrimidine Ring;Synlett;2023-10-18

3. Approaches to the synthesis of heterocyclic C-nucleosides;Russian Chemical Bulletin;2023-02

4. Bicyclic 5-6 Systems With One Bridgehead (Ring Junction) Nitrogen Atom: Three Extra Heteroatoms 1:2;Comprehensive Heterocyclic Chemistry IV;2022

5. Pyrazolotriazines: Biological activities, synthetic strategies and recent developments;European Journal of Medicinal Chemistry;2021-11

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