(Q59667181)

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

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

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2

Jacek Stawinski

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Adam Kraszewski

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1

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Adam Kraszewski

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publication date

1 January 2007

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published in

Pure and Applied Chemistry

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volume

79

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issue

12

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page(s)

2217-2227

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cites work

Cholesteryl-conjugated oligonucleotides: synthesis, properties, and activity as inhibitors of replication of human immunodeficiency virus in cell culture

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Chemical and Structural Diversity of siRNA Molecules

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Nucleoside H-phosphonates. III. Chemical synthesis of oligodeoxyribonucleotides by the hydrogenphosphonate approach

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No d Orbitals but Walsh Diagrams and Maybe Banana Bonds: Chemical Bonding in Phosphines, Phosphine Oxides, and Phosphonium Ylides

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NucleosideH-Phosphonates. 18. Synthesis of Unprotected Nucleoside 5‘-H-Phosphonates and Nucleoside 5‘-H-Phosphonothioates and Their Conversion into the 5‘-Phosphorothioate and 5‘-Phosphorodithioate Monoesters

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Aryl H-phosphonates. 12. Synthetic and (31)P NMR studies on the preparation of nucleoside H-phosphonothioate and nucleoside H-phosphonodithioate monoesters

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Deoxynucleoside H-Phosphonate diester intermediates in the synthesis of internucleotide phosphate analogues

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Nucleoside H-Phosphonates XX. Efficient Method for the Preparation of Nucleoside H-Phosphonoselenoate Monoesters

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Prodrugs of biologically active phosphate esters

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Dipentafluorophenyl carbonate--a reagent for the synthesis of oligonucleotides and their conjugates

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Silylation-Mediated Transesterification ofO-Phenyl H-Phosphonothioates − A New Entry to Nucleoside H-Phosphonothioate Monoesters

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Efficient synthesis of oligoribonucleotide and its phosphorothioate analogue using H-phosphonate approach

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Aryl nucleoside H-phosphonates. Part 15: Synthesis, properties and, anti-HIV activity of aryl nucleoside 5'-alpha-hydroxyphosphonates

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High Stereoselectivity in the Formation of the Inter-Ribonucleotidic Phosphorothioate Bond

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Synthesis of DNA via deoxynucleoside H-phosphonate intermediates

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Nucleoside H-Phosphonates. 17. Synthetic and (31)P NMR Studies on the Preparation of Dinucleoside H-Phosphonothioates

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Nucleoside Phosphonates. Development of Synthetic Methods and Reagents

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A new and versatile approach to the preparation of valuable deoxynucleoside 3′-phosphite intermediates

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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

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Natural phosphoglycans containing glycosyl phosphate units: structural diversity and chemical synthesis

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Antisense oligonucleotides: a new therapeutic principle

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Studies on phosphorylation; further observations on the reaction of phosphites with polyhalogen compounds in presence of bases and its application to the phosphorylation of alcohols

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How to get the most out of two phosphorus chemistries. Studies on H-phosphonates

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BIOLOGICAL ACTIVITY OF AMINOPHOSPHONIC ACIDS

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Letter: Silyl phosphites. I. The reaction of silyl phosphites with diphenyl disulfide. Synthesis of S-phenyl nucleoside phosphorothioates.

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Chemical Synthesis of Oligodeoxyribonucleotides UsingN-UnprotectedH-Phosphonate Monomers and Carbonium and Phosphonium Condensing Reagents: O-Selective Phosphonylation and Condensation

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ArylH-Phosphonates. 14. Synthesis of New Nucleotide Analogues with Phosphonate−Phosphate Internucleosidic Linkage

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gem-Diphosphonate and gem-phosphonate-phosphate compounds with specific high density lipoprotein inducing activity

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Why nature chose phosphates

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ArylH-Phosphonates. 6. Synthetic Studies on the Preparation of NucleosideN-Alkyl-H-phosphonamidates

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Synthesis of new classes of boron-containing nucleotides

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10.1351/PAC200779122217

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(Q59667181)

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

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