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Nucleotides. XL: Synthesis and characterization of modified 2'-5'-adenylate trimers-potential antiviral agents

Helvetica chimica acta, 1994, Vol.77 (1), p.10-22

1994

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Inhibition of HIV-1 Replication and Activation of RNase L by Phosphorothioate/Phosphodiester 2′,5′-Oligoadenylate Derivatives (∗)

The Journal of biological chemistry, 1995-03, Vol.270 (11), p.5963-5978

1995

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New approach to automated synthesis of oligoribonucleotides

Nucleic acids symposium series (1979), 1987 (18), p.205-208

1987

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Base Labile Protecting Groups for Hydroxyl Functions in Ribonucleosides and Deoxyribonucleosides

Nucleosides & nucleotides, 1987-01, Vol.6 (1-2), p.501-503

1987

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Nucleosides. LI: The 2-(4-nitrophenyl)ethoxycarbonyl (npeoc) and 2-(2,4-dinitrophenyl)ethoxycarbonyl (dnpeoc) groups for protection of hydroxy functions in ribonucleosides and 2'-deoxyribonucleosides

Helvetica chimica acta, 1993, Vol.76 (1), p.385-401

1993

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ChemInform Abstract: Direct Immobilization of Oligonucleotides on Polymer Supports: Use of FMOC Derivatives in DNA/RNA Synthesis - Methods for Using Immobilized Oligonucleotides

ChemInform, 2002-08, Vol.33 (32), p.no-no

2002

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Nucleotides, Part LIX , Synthesis, Characterization, and Biological Activities of New Potential Antiviral Agents: (2′ - 5′)Adenylate Trimer Analogs Containing 3′-Deoxy-3′-(hexadecanoylamino)adenosine at the 2′-Terminus

Helvetica chimica acta, 1999-04, Vol.82 (4), p.597-613

1999

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The p-Nitrophenylethyl Group - An Universal Blocking Group in Nucleoside and Nucleotide Chemistry

Nucleosides & nucleotides, 1985-02, Vol.4 (1-2), p.81-94

1985

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ChemInform Abstract: The 9-Fluorenylmethoxycarbonyl (Fmoc) Group and Its Use in Oligonucleotide Synthesis

ChemInform, 1999-10, Vol.30 (43), p.no-no

1999

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The 9-Fluorenylmethoxycarbonyl (Fmoc) Group and Its Use in Oligonucleotide Synthesis

Nucleosides & nucleotides, 1999-06, Vol.18 (6-7), p.1219-1220

1999

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ChemInform Abstract: Nucleotides. Part 40. Synthesis and Characterization of Modified 2′-5′ Adenylate Trimers - Potential Antiviral Agents

ChemInform, 1994-05, Vol.25 (20), p.no-no

1994

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ber die Analyse titanhaltiger K rper

Analytical and bioanalytical chemistry, 1912-07, Vol.51 (7-8), p.498-504

1912

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ChemInform Abstract: Nucleosides. Part 51. The 2-(4-Nitrophenyl)ethoxycarbonyl (npeoc) and 2-(2,4-Dinitrophenyl)ethoxycarbonyl (dnpeoc) Groups for Protection of Hydroxy Functions in Ribonucleosides and 2′-Deoxyribonucleosides

ChemInform, 1993-06, Vol.24 (26), p.no-no

1993

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3D printing of high density polyethylene by fused filament fabrication

Additive manufacturing, 2019-08, Vol.28, p.152-159

2019

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ChemInform Abstract: New Developments in Nucleotide Chemistry

Chemischer Informationsdienst, 1986-09, Vol.17 (38)

1986

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Cytotoxicity of polymers intended for the extrusion-based additive manufacturing of surgical guides

Scientific reports, 2022-05, Vol.12 (1), p.7391-7391, Article 7391

2022

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Unlocking Cancer Glycomes from Histopathological Formalin-fixed and Paraffin-embedded (FFPE) Tissue Microdissections

Molecular & cellular proteomics, 2017-04, Vol.16 (4), p.524-536

2017

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Post-Column Make-Up Flow (PCMF) Enhances the Performance of Capillary-Flow PGC-LC-MS/MS-Based Glycomics

Analytical chemistry (Washington), 2019-04, Vol.91 (7), p.4559-4567

2019

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Pandemic-Driven Development of a Medical-Grade, Economic and Decentralized Applicable Polyolefin Filament for Additive Fused Filament Fabrication

Molecules (Basel, Switzerland), 2020-12, Vol.25 (24), p.5929

2020

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ChemInform Abstract: Nucleosides. Part 59. The 2-(4-Nitrophenyl)ethylsulfonyl (Npes) Group: A New Type of Protection in Nucleoside Chemistry

ChemInform, 1996-02, Vol.27 (6), p.no-no

1996

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Bycatch in gillnet fisheries – An overlooked threat to waterbird populations

Biological conservation, 2009-07, Vol.142 (7), p.1269-1281

2009

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Model Studies Towards the Automated Synthesis of tRNAs

Nucleosides & nucleotides, 1991-01, Vol.10 (1-3), p.377-382

1991

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ChemInform Abstract: The p‐Nitrophenylethyl Group ‐ a Universal Blocking Group in Nucleoside and Nucleotide Chemistry

Chemischer Informationsdienst, 1986-03, Vol.17 (11)

1986

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Bacteria from the Amycolatopsis genus associated with a toxic bird secrete protective secondary metabolites

Nature communications, 2024-10, Vol.15 (1), p.8524-16, Article 8524

2024

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Flagellin Glycoproteomics of the Periodontitis Associated Pathogen Selenomonas sputigena Reveals Previously Not Described O-glycans and Rhamnose Fragment Rearrangement Occurring on the Glycopeptides

Molecular & cellular proteomics, 2018-04, Vol.17 (4), p.721-736

2018

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Nucleotides. XL: Synthesis and characterization of modified 2'-5'-adenylate trimers-potential antiviral agents

Inhibition of HIV-1 Replication and Activation of RNase L by Phosphorothioate/Phosphodiester 2′,5′-Oligoadenylate Derivatives (∗)

New approach to automated synthesis of oligoribonucleotides

Base Labile Protecting Groups for Hydroxyl Functions in Ribonucleosides and Deoxyribonucleosides

Nucleosides. LI: The 2-(4-nitrophenyl)ethoxycarbonyl (npeoc) and 2-(2,4-dinitrophenyl)ethoxycarbonyl (dnpeoc) groups for protection of hydroxy functions in ribonucleosides and 2'-deoxyribonucleosides

ChemInform Abstract: Direct Immobilization of Oligonucleotides on Polymer Supports: Use of FMOC Derivatives in DNA/RNA Synthesis - Methods for Using Immobilized Oligonucleotides

Nucleotides, Part LIX , Synthesis, Characterization, and Biological Activities of New Potential Antiviral Agents: (2′ - 5′)Adenylate Trimer Analogs Containing 3′-Deoxy-3′-(hexadecanoylamino)adenosine at the 2′-Terminus

The p-Nitrophenylethyl Group - An Universal Blocking Group in Nucleoside and Nucleotide Chemistry

ChemInform Abstract: The 9-Fluorenylmethoxycarbonyl (Fmoc) Group and Its Use in Oligonucleotide Synthesis

The 9-Fluorenylmethoxycarbonyl (Fmoc) Group and Its Use in Oligonucleotide Synthesis

ChemInform Abstract: Nucleotides. Part 40. Synthesis and Characterization of Modified 2′-5′ Adenylate Trimers - Potential Antiviral Agents

ber die Analyse titanhaltiger K rper

ChemInform Abstract: Nucleosides. Part 51. The 2-(4-Nitrophenyl)ethoxycarbonyl (npeoc) and 2-(2,4-Dinitrophenyl)ethoxycarbonyl (dnpeoc) Groups for Protection of Hydroxy Functions in Ribonucleosides and 2′-Deoxyribonucleosides

3D printing of high density polyethylene by fused filament fabrication

ChemInform Abstract: New Developments in Nucleotide Chemistry

Cytotoxicity of polymers intended for the extrusion-based additive manufacturing of surgical guides

Unlocking Cancer Glycomes from Histopathological Formalin-fixed and Paraffin-embedded (FFPE) Tissue Microdissections

Post-Column Make-Up Flow (PCMF) Enhances the Performance of Capillary-Flow PGC-LC-MS/MS-Based Glycomics

Pandemic-Driven Development of a Medical-Grade, Economic and Decentralized Applicable Polyolefin Filament for Additive Fused Filament Fabrication

ChemInform Abstract: Nucleosides. Part 59. The 2-(4-Nitrophenyl)ethylsulfonyl (Npes) Group: A New Type of Protection in Nucleoside Chemistry

Bycatch in gillnet fisheries – An overlooked threat to waterbird populations

Model Studies Towards the Automated Synthesis of tRNAs

ChemInform Abstract: The p‐Nitrophenylethyl Group ‐ a Universal Blocking Group in Nucleoside and Nucleotide Chemistry

Bacteria from the Amycolatopsis genus associated with a toxic bird secrete protective secondary metabolites

Flagellin Glycoproteomics of the Periodontitis Associated Pathogen Selenomonas sputigena Reveals Previously Not Described O-glycans and Rhamnose Fragment Rearrangement Occurring on the Glycopeptides

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