Development of O–H insertion for the attachment of phosphonates to nucleosides; synthesis of α-carboxy phosphononucleosides-Reference-Cited by-同舟云学术

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Development of O–H insertion for the attachment of phosphonates to nucleosides; synthesis of α-carboxy phosphononucleosides

Published:2012-02 Issue:7 Volume:68 Page:1894-1909
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Hladezuk Isabelle,Chastagner Veronique,Collins Stuart G.,Plunkett Stephen J.,Ford Alan,Debarge Sebastien,Maguire Anita R.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference99 articles.

1. Antivirals: current state of the art

2. Anti-HIV drugs: 25 compounds approved within 25 years after the discovery of HIV

3. Improving AZT efficacy

4. Design of Anti-HIV Compounds from Nucleoside to Nucleoside 5-Triphosphate Analogs. Problems and Perspectives

5. The acyclic nucleoside phosphonates from inception to clinical use: Historical perspective

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1. Synthesis and Evaluation of Prodrugs of α-Carboxy Nucleoside Phosphonates;The Journal of Organic Chemistry;2022-10-25

2. Tenofovir-Amino Acid Conjugates Act as Polymerase Substrates—Implications for Avoiding Cellular Phosphorylation in the Discovery of Nucleotide Analogues;Journal of Medicinal Chemistry;2020-12-23

3. The McKenna reaction – avoiding side reactions in phosphonate deprotection;Beilstein Journal of Organic Chemistry;2020-06-23

4. Recent advances in the synthesis of cyclic 5′-nornucleoside phosphonate analogues;Carbohydrate Research;2018-06

5. λ5-Phosphorus-Containing α-Diazo Compounds: A Valuable Tool for Accessing Phosphorus-Functionalized Molecules;Chemical Reviews;2016-10-24

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