Synthesis of 2′-Deoxy-9-deaza Nucleosides Using Heck Methodology
Author:
Affiliation:
1. University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, Maryland 21250, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo400913k
Reference30 articles.
1. Synthesis and Antitumor Activity of Thieno-Separated Tricyclic Purines
2. “Fleximers”. Design and Synthesis of a New Class of Novel Shape-Modified Nucleosides1
3. Hetero-expanded Purine Nucleosides. Design, Synthesis and Preliminary Biological Activity
4. Tricyclic 2′-C-Modified Nucleosides as Potential Anti-HCV Therapeutics
5. Synthesis of a Novel C-Nucleoside, 2-Amino-7-(2-deoxy-β- D-erythro-pentofuranosyl)-3H,5H-pyrrolo-[3,2-d]pyrimidin-4-one (2′-Deoxy-9-deazaguanosine)
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1. Synthesis of Aryl or Heteroaryl C-Nucleosides by Direct Coupling of a Carbohydrate Moiety with a Preformed Aglycon Unit;Chinese Journal of Organic Chemistry;2021
2. Total synthesis of pseudouridine via Heck-type C-glycosylation;New Journal of Chemistry;2019
3. Arylhydrazones Derivatives Containing a Benzothiazole Moiety, Efficient Ligands in the Palladium-Catalyzed Mizoroki-Heck and Suzuki-Miyaura Cross-coupling Reactions under IR Irradiation;Chinese Journal of Chemistry;2017-09-05
4. Novel carbon nanofiber-supported Ni(0) nanoparticles catalyse the Heck reaction under ligand-free conditions;RSC Advances;2016
5. Antiproliferative activities of halogenated pyrrolo[3,2-d]pyrimidines;Bioorganic & Medicinal Chemistry;2015-08
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