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Terminal lipophilization of a unique DNA dodecamer by various nucleolipid headgroups: Their incorporation into artificial lipid bilayers and hydrodynamic properties

Beilstein journal of organic chemistry, 2015-06, Vol.11 (1), p.913-929

2015

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Specific DNA duplex formation at an artificial lipid bilayer: fluorescence microscopy after Sybr Green I staining

Beilstein journal of organic chemistry, 2014-10, Vol.10 (1), p.2307-2321

2014

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1′, 5′ -Anhydrohexitol Oligonucleotides: Synthesis, Base Pairing and Recognition by Regular Oligodeoxyribonucleotides and Oligoribonucleotides

Chemistry : a European journal, 1997-01, Vol.3 (1), p.110-120

1997

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Synthesis of Functionalized Lipids, and Their Use for a Tunable Hydrophobization of Nucleosides and Nucleic Acids

Helvetica chimica acta, 2013-02, Vol.96 (2), p.201-216

2013

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O-2′,3′-Ketal-Nucleolipids of the Cytostatic 5-Fluorouridine: Synthesis, Lipophilicity, and Acidic Stability

Helvetica chimica acta, 2010-08, Vol.93 (8), p.1500-1512

2010

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1,N6-Etheno-2′-deoxytubercidin and pyrrolo-C: synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides

Tetrahedron, 2007-04, Vol.63 (17), p.3471-3482

2007

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1′,5′-Anhydrohexitol Oligonucleotides: Hybridisation and Strand Displacement with Oligoribonucleotides, Interaction with RNase H and HIV Reverse Transcriptase

Chemistry : a European journal, 1997-09, Vol.3 (9), p.1513-1520

1997

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Electrophilic Substitution at C(7) of a Protected 7-Deaza-2’-deoxyguanosine – The 2’-Deoxyribonucleoside Parent Analogue of Queuosine

MolBank, 2007-04, Vol.2007 (1), p.M522

2007

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Synthesis and Pairing Properties of Oligonucleotides Containing 3-Hydroxy-4-hydroxymethyl-1-cyclohexanyl Nucleosides

Chemistry : a European journal, 1999-07, Vol.5 (7), p.2139-2150

1999

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Combinatorial Synthesis of New Pyrimidine‐ and Purine‐β‐d‐Ribonucleoside Nucleolipids: Their Distribution Between Aqueous and Organic Phases and Their In Vitro Activity Against Human‐ and Rat Glioblastoma Cells In Vitro

Chemistry & biodiversity, 2018-09, Vol.15 (9), p.e1800173-n/a

2018

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Front Cover: Nucleolipids of the Nucleoside Antibiotics Formycins A and B: Synthesis and Biomedical Characterization Particularly Using Glioblastoma Cells (C&B 4/2019)

Chemistry & biodiversity, 2019-04, Vol.16 (4), p.n/a

2019

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Synthesis of New Potential Lipophilic Co‐Drugs of 2‐Chloro‐2′‐deoxyadenosine (Cladribine, 2‐CdA, Mavenclad®, Leustatin®) and 6‐Azauridine (z6U) with Valproic Acid

Chemistry & biodiversity, 2019-03, Vol.16 (3), p.e1800497-n/a

2019

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Solution Structure and Conformational Dynamics of Deoxyxylonucleic Acids (dXNA): An Orthogonal Nucleic Acid Candidate

Chemistry : a European journal, 2012-01, Vol.18 (3), p.869-879

2012

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Synthesis of 3-(4-Chloro-2-methoxy-7H-pyrrolo[2,3-d]-pyrimidin-7-yl)propanoic acid – An N(9)-Functionalized 7-Deazapurine

MolBank, 2009-03, Vol.2009 (1), p.M590

Rosemeyer, Helmut

2009

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Novel Nucleolipids of Pyrimidine [beta]-D-Ribonucleosides: Combinatorial Synthesis, Spectroscopic Characterization, and Cytostatic/Cytotoxic Activities

Chemistry & biodiversity, 2016-02, Vol.13 (2), p.160

2016

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Synthesis of Thymidine, Uridine, and 5-Methyluridine Nucleolipids: Tools for a Tuned Lipophilization of Oligonucleotides

Helvetica chimica acta, 2013-05, Vol.96 (5), p.872-888

2013

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Synthesis of New Potential Lipophilic Co-Drugs of 2-Chloro-2'-deoxyadenosine (Cladribine, 2-CdA, Mavenclad®, Leustatin®) and 6-Azauridine (z 6 U) with Valproic Acid

Chemistry & biodiversity, 2018-12

2018

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Interaction of Viologens with Nucleic Acid G-Tetrades

Langmuir, 2008-06, Vol.24 (11), p.5641-5643

2008

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1, N 6-Etheno-2′-deoxytubercidin and pyrrolo-C: synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides

Tetrahedron, 2007-04, Vol.63 (17), p.3471-3482

2007

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Nucleolipids of Canonical Purine ß‐d‐Ribo‐Nucleosides: Synthesis and Cytostatic/Cytotoxic Activities Toward Human and Rat Glioblastoma Cells

ChemistryOpen (Weinheim), 2016-04, Vol.5 (2), p.129-141

2016

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Synthesis of 3-(4-Amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)propanoic acid – A Functionalized Base Derivative of the Nucleoside Antibiotic Tubercidin

MolBank, 2007-08, Vol.2007 (4), p.M555

Rosemeyer, Helmut

2007

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Nucleolipids of Canonical Purine s-d-Ribo-Nucleosides: Synthesis and Cytostatic/Cytotoxic Activities Toward Human and Rat Glioblastoma Cells

ChemistryOpen (Weinheim), 2016-04, Vol.5 (2), p.129-141

2016

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Cyclohexene Nucleic Acids (CeNA): Serum Stable Oligonucleotides that Activate RNase H and Increase Duplex Stability with Complementary RNA

Journal of the American Chemical Society, 2000-09, Vol.122 (36), p.8595-8602

2000

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Synthesis and Crystal Structures of O-2′,3′-Cyclic Cyclopentanone and Cyclohexanone Ketals of the Cytostatic 5-Fluorouridine

Helvetica chimica acta, 2009-10, Vol.92 (10), p.1923-1932

2009

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Synthesis and Crystal Structures of Two 9-(2-Bromoethyl)-Substituted 7-Deazapurines

Helvetica chimica acta, 2009-10, Vol.92 (10), p.1944-1951

2009

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Terminal lipophilization of a unique DNA dodecamer by various nucleolipid headgroups: Their incorporation into artificial lipid bilayers and hydrodynamic properties

Specific DNA duplex formation at an artificial lipid bilayer: fluorescence microscopy after Sybr Green I staining

1′, 5′ -Anhydrohexitol Oligonucleotides: Synthesis, Base Pairing and Recognition by Regular Oligodeoxyribonucleotides and Oligoribonucleotides

Synthesis of Functionalized Lipids, and Their Use for a Tunable Hydrophobization of Nucleosides and Nucleic Acids

O-2′,3′-Ketal-Nucleolipids of the Cytostatic 5-Fluorouridine: Synthesis, Lipophilicity, and Acidic Stability

1,N6-Etheno-2′-deoxytubercidin and pyrrolo-C: synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides

1′,5′-Anhydrohexitol Oligonucleotides: Hybridisation and Strand Displacement with Oligoribonucleotides, Interaction with RNase H and HIV Reverse Transcriptase

Electrophilic Substitution at C(7) of a Protected 7-Deaza-2’-deoxyguanosine – The 2’-Deoxyribonucleoside Parent Analogue of Queuosine

Synthesis and Pairing Properties of Oligonucleotides Containing 3-Hydroxy-4-hydroxymethyl-1-cyclohexanyl Nucleosides

Combinatorial Synthesis of New Pyrimidine‐ and Purine‐β‐d‐Ribonucleoside Nucleolipids: Their Distribution Between Aqueous and Organic Phases and Their In Vitro Activity Against Human‐ and Rat Glioblastoma Cells In Vitro

Front Cover: Nucleolipids of the Nucleoside Antibiotics Formycins A and B: Synthesis and Biomedical Characterization Particularly Using Glioblastoma Cells (C&B 4/2019)

Synthesis of New Potential Lipophilic Co‐Drugs of 2‐Chloro‐2′‐deoxyadenosine (Cladribine, 2‐CdA, Mavenclad®, Leustatin®) and 6‐Azauridine (z6U) with Valproic Acid

Solution Structure and Conformational Dynamics of Deoxyxylonucleic Acids (dXNA): An Orthogonal Nucleic Acid Candidate

Synthesis of 3-(4-Chloro-2-methoxy-7H-pyrrolo[2,3-d]-pyrimidin-7-yl)propanoic acid – An N(9)-Functionalized 7-Deazapurine

Novel Nucleolipids of Pyrimidine [beta]-D-Ribonucleosides: Combinatorial Synthesis, Spectroscopic Characterization, and Cytostatic/Cytotoxic Activities

Synthesis of Thymidine, Uridine, and 5-Methyluridine Nucleolipids: Tools for a Tuned Lipophilization of Oligonucleotides

Synthesis of New Potential Lipophilic Co-Drugs of 2-Chloro-2'-deoxyadenosine (Cladribine, 2-CdA, Mavenclad®, Leustatin®) and 6-Azauridine (z 6 U) with Valproic Acid

Interaction of Viologens with Nucleic Acid G-Tetrades

1, N 6-Etheno-2′-deoxytubercidin and pyrrolo-C: synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides

Nucleolipids of Canonical Purine ß‐d‐Ribo‐Nucleosides: Synthesis and Cytostatic/Cytotoxic Activities Toward Human and Rat Glioblastoma Cells

Synthesis of 3-(4-Amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)propanoic acid – A Functionalized Base Derivative of the Nucleoside Antibiotic Tubercidin

Nucleolipids of Canonical Purine s-d-Ribo-Nucleosides: Synthesis and Cytostatic/Cytotoxic Activities Toward Human and Rat Glioblastoma Cells

Cyclohexene Nucleic Acids (CeNA): Serum Stable Oligonucleotides that Activate RNase H and Increase Duplex Stability with Complementary RNA

Synthesis and Crystal Structures of O-2′,3′-Cyclic Cyclopentanone and Cyclohexanone Ketals of the Cytostatic 5-Fluorouridine

Synthesis and Crystal Structures of Two 9-(2-Bromoethyl)-Substituted 7-Deazapurines

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