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H-Phosphonate Chemistry in the Synthesis of Electrically Neutral and Charged Antiviral and Anticancer Pronucleotides

Frontiers in chemistry, 2020-11, Vol.8, p.595738-595738

2020

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H-Phosphonates: Versatile synthetic precursors to biologically active phosphorus compounds

Pure and applied chemistry, 2007-01, Vol.79 (12), p.2217-2227

2007

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How To Get the Most Out of Two Phosphorus Chemistries. Studies on H-Phosphonates

Accounts of chemical research, 2002-11, Vol.35 (11), p.952-960

2002

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Stereochemistry of internucleotide bond formation by the H-phosphonate method. Part 3: Investigations on a mechanism of asymmetric induction

Tetrahedron: asymmetry, 2007-09, Vol.18 (19), p.2336-2348

2007

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The role of nucleophilic catalysis in chemistry and stereochemistry of ribonucleosideH-phosphonate condensation

New journal of chemistry, 2009, Vol.33 (1), p.164-170

2009

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Nucleoside 3′,5′-Cyclic H‑Phosphonates, New Useful Precursors for the Synthesis of Nucleoside 3′,5′-Cyclic Phosphates and Their Analogues

Organic letters, 2013-08, Vol.15 (16), p.4082-4085

2013

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Aryl H-phosphonates. 19. New anti-HIV pronucleotide phosphoramidate diesters containing amino- and hydroxypyridine auxiliaries

European journal of medicinal chemistry, 2019-02, Vol.164, p.47-58

2019

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New antiglioma zwitterionic pronucleotides with an FdUMP framework

European journal of medicinal chemistry, 2018-01, Vol.144, p.682-691

2018

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The case of triethylammonium cation loss during purification of certain nucleotide analogues: a cautionary note

Analytical and bioanalytical chemistry, 2015-02, Vol.407 (6), p.1775-1780

2015

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A New, Efficient Entry to Non-Lipophilic H-Phosphonate Monoesters – Preparation of Anti-HIV Nucleotide Analogues

Letters in organic chemistry, 2009-09, Vol.6 (6), p.496-499

2009

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Recent advances in H-phosphonate chemistry. Part 1. H-phosphonate esters: synthesis and basic reactions

Topics in current chemistry, 2015, Vol.361, p.137

2015

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Aryl H-Phosphonates 18. Synthesis, properties, and biological activity of 2′,3′-dideoxynucleoside (N-heteroaryl)phosphoramidates of increased lipophilicity

European journal of medicinal chemistry, 2015-07, Vol.100, p.77-88

2015

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Studies on aryl H-phosphonates. I. An efficient method for the preparation of deoxyribo- and ribonucleoside 3′-H-phosphonate monoesters by transesterification of diphenyl H-phosphonate

Tetrahedron letters, 1994-05, Vol.35 (20), p.3355-3358

1994

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New 3′-O-aromatic acyl-5-fluoro-2′-deoxyuridine derivatives as potential anticancer agents

European journal of medicinal chemistry, 2016-06, Vol.115, p.41-52

2016

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Searching for anti-glioma activity. Ribonucleoside analogues with modifications in nucleobase and sugar moieties

Acta biochimica Polonica, 2016-01, Vol.63 (4), p.765

2016

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The role of nucleophilic catalysis in chemistry and stereochemistry of ribonucleoside H -phosphonate condensation

New journal of chemistry, 2009, Vol.33 (1), p.164

2009

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Stereochemistry of internucleotide bond formation by the H-phosphonate method. 7. Stereoselective formation of ribonucleoside ( R P)- and ( S P)-3′- H-phosphonothioate monoesters

Tetrahedron: asymmetry, 2010-03, Vol.21 (4), p.410-419

2010

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Novel reactivity of Fhit proteins: catalysts for fluorolysis of nucleoside 5'-phosphoramidates and nucleoside 5'-phosphosulfates to generate nucleoside 5'-phosphorofluoridates

Biochemical journal, 2015-06, Vol.468 (2), p.337-344

2015

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Chemical and Stereochemical Aspects of Oxidative Coupling of HPhosphonate and H-Phosphonothioate Diesters. Reactions with N,N-, N,Oand O,O-Binucleophiles

Letters in organic chemistry, 2005-03, Vol.2 (2), p.188-197

2005

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Studies on the decomposition pathways of diastereoisomeric mixtures of aryl nucleoside [small alpha]-hydroxyphosphonates under hydrolytic conditions. Synthesis of [small alpha]-hydroxyphosphonate monoesters

New journal of chemistry, 2010-01, Vol.34 (5), p.976-983

2010

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Stereochemistry of internucleotide bond formation by the H-phosphonate method. Part 6: Optimization of the reaction conditions towards highest stereoselectivity

Tetrahedron: asymmetry, 2008-11, Vol.19 (21), p.2508-2518

2008

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Aryl H-Phosphonates. 6. Synthetic Studies on the Preparation of Nucleoside N-Alkyl-H-phosphonamidates

Journal of organic chemistry, 1997-07, Vol.62 (14), p.4791-4794

1997

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Aryl H-Phosphonates 17: (N-Aryl)phosphoramidates of Pyrimidine Nucleoside Analogues and Their Synthesis, Selected Properties, and Anti-HIV Activity

Journal of medicinal chemistry, 2011-10, Vol.54 (19), p.6482-6491

2011

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Aryl Hphosphonates. 8. Simple and efficient method forv the preparation of nucleoside Hphosphonothioate monoesters

Tetrahedron letters, 1999-05, Vol.40 (20), p.3945-3948

1999

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Studies on the decomposition pathways of diastereoisomeric mixtures of aryl nucleoside α-hydroxyphosphonates under hydrolytic conditions. Synthesis of α-hydroxyphosphonate monoestersThis paper is dedicated to Prof. Dr Wojciech J. Stec, Center of Molecular and Macromolecular Studies, Polish Academy of Sciences, ód , Poland, on the occasion of his 70th birthday. This article is part of a themed issue on Biophosphates

2010-05

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H-Phosphonate Chemistry in the Synthesis of Electrically Neutral and Charged Antiviral and Anticancer Pronucleotides

H-Phosphonates: Versatile synthetic precursors to biologically active phosphorus compounds

How To Get the Most Out of Two Phosphorus Chemistries. Studies on H-Phosphonates

Stereochemistry of internucleotide bond formation by the H-phosphonate method. Part 3: Investigations on a mechanism of asymmetric induction

The role of nucleophilic catalysis in chemistry and stereochemistry of ribonucleosideH-phosphonate condensation

Nucleoside 3′,5′-Cyclic H‑Phosphonates, New Useful Precursors for the Synthesis of Nucleoside 3′,5′-Cyclic Phosphates and Their Analogues

Aryl H-phosphonates. 19. New anti-HIV pronucleotide phosphoramidate diesters containing amino- and hydroxypyridine auxiliaries

New antiglioma zwitterionic pronucleotides with an FdUMP framework

The case of triethylammonium cation loss during purification of certain nucleotide analogues: a cautionary note

A New, Efficient Entry to Non-Lipophilic H-Phosphonate Monoesters – Preparation of Anti-HIV Nucleotide Analogues

Recent advances in H-phosphonate chemistry. Part 1. H-phosphonate esters: synthesis and basic reactions

Aryl H-Phosphonates 18. Synthesis, properties, and biological activity of 2′,3′-dideoxynucleoside (N-heteroaryl)phosphoramidates of increased lipophilicity

Studies on aryl H-phosphonates. I. An efficient method for the preparation of deoxyribo- and ribonucleoside 3′-H-phosphonate monoesters by transesterification of diphenyl H-phosphonate

New 3′-O-aromatic acyl-5-fluoro-2′-deoxyuridine derivatives as potential anticancer agents

Searching for anti-glioma activity. Ribonucleoside analogues with modifications in nucleobase and sugar moieties

The role of nucleophilic catalysis in chemistry and stereochemistry of ribonucleoside H -phosphonate condensation

Stereochemistry of internucleotide bond formation by the H-phosphonate method. 7. Stereoselective formation of ribonucleoside ( R P)- and ( S P)-3′- H-phosphonothioate monoesters

Novel reactivity of Fhit proteins: catalysts for fluorolysis of nucleoside 5'-phosphoramidates and nucleoside 5'-phosphosulfates to generate nucleoside 5'-phosphorofluoridates

Chemical and Stereochemical Aspects of Oxidative Coupling of HPhosphonate and H-Phosphonothioate Diesters. Reactions with N,N-, N,Oand O,O-Binucleophiles

Studies on the decomposition pathways of diastereoisomeric mixtures of aryl nucleoside [small alpha]-hydroxyphosphonates under hydrolytic conditions. Synthesis of [small alpha]-hydroxyphosphonate monoesters

Stereochemistry of internucleotide bond formation by the H-phosphonate method. Part 6: Optimization of the reaction conditions towards highest stereoselectivity

Aryl H-Phosphonates. 6. Synthetic Studies on the Preparation of Nucleoside N-Alkyl-H-phosphonamidates

Aryl H-Phosphonates 17: (N-Aryl)phosphoramidates of Pyrimidine Nucleoside Analogues and Their Synthesis, Selected Properties, and Anti-HIV Activity

Aryl Hphosphonates. 8. Simple and efficient method forv the preparation of nucleoside Hphosphonothioate monoesters

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