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CO2-free hydrogen as a substitute to fossil fuels: What are the targets? Prospective assessment of the hydrogen market attractiveness

International journal of hydrogen energy, 2012-06, Vol.37 (12), p.9451-9458

2012

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New bis(SATE) prodrug of AZT 5′‐monophosphate: In vitro anti‐HIV activity, stability, and potential oral absorption

Journal of pharmaceutical sciences, 2001-04, Vol.90 (4), p.448-463

2001

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Comparative evaluation of seven oligonucleotide analogs as potential antisense agents

Journal of medicinal chemistry, 1993, Vol.36 (2), p.280-287

1993

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Synthesis of ( Z) and ( E) α-alkenyl phosphonic acid derivatives of purines and pyrimidines

Tetrahedron, 1998-04, Vol.54 (15), p.3807-3816

1998

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Use of MALDI-TOF mass spectrometry to monitor solid-phase synthesis of oligonucleotides

Analytical and bioanalytical chemistry, 2002-09, Vol.374 (1), p.57-63

2002

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Anti-HIV pronucleotides: Decomposition pathways and correlation with biological activities

Bioorganic & medicinal chemistry letters, 1998-05, Vol.8 (9), p.1045-1050

1998

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Use of 2-( tert-butyldiphenylsilyloxymethyl) benzoyl as N-protecting group for the synthesis of prooligonucleotides

Bioorganic & medicinal chemistry letters, 2001-11, Vol.11 (21), p.2813-2816

2001

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First synthesis of alternating SATE-phosphotriester/ phosphodiester prooligonucleotides on solid support

Bioorganic & medicinal chemistry letters, 1998-10, Vol.8 (20), p.2913-2918

1998

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Rational design of a new series of mixed anti-HIV pronucleotides

Bioorganic & medicinal chemistry letters, 1998-11, Vol.8 (21), p.3003-3006

1998

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Synthesis of New Bis-Alkylated Phosphono Alkenyl Acyclonucleosides : (Z) and (E)-Diethyl-2-(3-alkyl pyrimidin-1-yl)ethylen-1-yl Phosphonate

Molecules (Basel, Switzerland), 2000-10, Vol.5 (10), p.1139-1145

2000

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Synthesis, Anti-HIV Activity, and Stability Studies of 5′-Phosphorofluoridate Derivatives of AZT

Bioorganic chemistry, 2001-12, Vol.29 (6), p.333-344

2001

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Comparison of the disposition of ester prodrugs of the antiviral agent 9-(2-phosphonylmethoxyethyl)adenine [PMEA] in Caco-2 monolayers

Pharmaceutical research, 1998-02, Vol.15 (2), p.239-245

1998

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Synthesis of new acyclic nucleoside phosphonic acids by Michael addition

Tetrahedron letters, 1996-07, Vol.37 (27), p.4701-4704

1996

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Kinetics study of the biotransformation of an oligonucleotide prodrug in cells extract by matrix-assisted laser desorption–ionization time-of-flight mass spectrometry

Journal of chromatography. B, Biomedical sciences and applications, 2001-03, Vol.753 (1), p.123-130

2001

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Rational design for cytosolic delivery of nucleoside monophosphates : SATE and DTE as enzyme-labile transient phosphate protecting groups

Bioorganic & medicinal chemistry letters, 1993-12, Vol.3 (12), p.2521-2526

1993

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NAC/MEA Conjugate: A New Potent Antioxidant which Increases the GSH Level in Various Cell Lines

Bioorganic & medicinal chemistry letters, 2001-05, Vol.11 (9), p.1189-1191

2001

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Rational design of a new series of pronucleotide

Bioorganic & medicinal chemistry letters, 2001-07, Vol.11 (13), p.1775-1777

2001

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Phosphopeptide Prodrug Bearing an S-Acyl-2-thioethyl Enzyme-Labile Phosphate Protection

Journal of organic chemistry, 1998-11, Vol.63 (23), p.8547-8550

1998

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1,2-di-O-acetyl-5-O-benzoyl-3-deoxy-L-erythro-pentofuran ose, a convenient precursor for the stereospecific synthesis of nucleoside analogues with the unnatural beta-L-configuration

Carbohydrate research, 2000-01, Vol.323 (1-4), p.226-229

2000

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Acyclic analogs of 3'-azido-3'-deoxythymidine as potential antiviral agents. Nucleoside synthesis by Michael addition

Journal of medicinal chemistry, 1989-01, Vol.32 (1), p.73-76

1989

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A mild method for fluorescein labeling of base-sensitive oligonucleotides on solid support

Tetrahedron letters, 2000-09, Vol.41 (38), p.7317-7321

2000

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Synthesis, thermal stability and reactivity towards 9-aminoellipticine of double-stranded oligonucleotides containing a true abasic site

Nucleic acids research, 1989-12, Vol.17 (24), p.10307-10319

1989

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A new reduction process in fast-atom bombardment mass spectrometry: Transformation of an azido group into an amino group

Rapid communications in mass spectrometry, 1993-08, Vol.7 (8), p.704-706

1993

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Synthesis and biological evaluation of isomeric dinucleoside monophosphates and monomethylphosphonates of 9-.beta.-D-arabinofuranosyladenine and related analogs

Journal of medicinal chemistry, 1988-10, Vol.31 (10), p.1897-1907

1988

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Synthesis, DNA binding and biological evaluation of synthetic precursors and novel analogs of netropsin

Journal of medicinal chemistry, 1989-05, Vol.32 (5), p.1074-1083

1989

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CO2-free hydrogen as a substitute to fossil fuels: What are the targets? Prospective assessment of the hydrogen market attractiveness

New bis(SATE) prodrug of AZT 5′‐monophosphate: In vitro anti‐HIV activity, stability, and potential oral absorption

Comparative evaluation of seven oligonucleotide analogs as potential antisense agents

Synthesis of ( Z) and ( E) α-alkenyl phosphonic acid derivatives of purines and pyrimidines

Use of MALDI-TOF mass spectrometry to monitor solid-phase synthesis of oligonucleotides

Anti-HIV pronucleotides: Decomposition pathways and correlation with biological activities

Use of 2-( tert-butyldiphenylsilyloxymethyl) benzoyl as N-protecting group for the synthesis of prooligonucleotides

First synthesis of alternating SATE-phosphotriester/ phosphodiester prooligonucleotides on solid support

Rational design of a new series of mixed anti-HIV pronucleotides

Synthesis of New Bis-Alkylated Phosphono Alkenyl Acyclonucleosides : (Z) and (E)-Diethyl-2-(3-alkyl pyrimidin-1-yl)ethylen-1-yl Phosphonate

Synthesis, Anti-HIV Activity, and Stability Studies of 5′-Phosphorofluoridate Derivatives of AZT

Comparison of the disposition of ester prodrugs of the antiviral agent 9-(2-phosphonylmethoxyethyl)adenine [PMEA] in Caco-2 monolayers

Synthesis of new acyclic nucleoside phosphonic acids by Michael addition

Kinetics study of the biotransformation of an oligonucleotide prodrug in cells extract by matrix-assisted laser desorption–ionization time-of-flight mass spectrometry

Rational design for cytosolic delivery of nucleoside monophosphates : SATE and DTE as enzyme-labile transient phosphate protecting groups

NAC/MEA Conjugate: A New Potent Antioxidant which Increases the GSH Level in Various Cell Lines

Rational design of a new series of pronucleotide

Phosphopeptide Prodrug Bearing an S-Acyl-2-thioethyl Enzyme-Labile Phosphate Protection

1,2-di-O-acetyl-5-O-benzoyl-3-deoxy-L-erythro-pentofuran ose, a convenient precursor for the stereospecific synthesis of nucleoside analogues with the unnatural beta-L-configuration

Acyclic analogs of 3'-azido-3'-deoxythymidine as potential antiviral agents. Nucleoside synthesis by Michael addition

A mild method for fluorescein labeling of base-sensitive oligonucleotides on solid support

Synthesis, thermal stability and reactivity towards 9-aminoellipticine of double-stranded oligonucleotides containing a true abasic site

A new reduction process in fast-atom bombardment mass spectrometry: Transformation of an azido group into an amino group

Synthesis and biological evaluation of isomeric dinucleoside monophosphates and monomethylphosphonates of 9-.beta.-D-arabinofuranosyladenine and related analogs

Synthesis, DNA binding and biological evaluation of synthetic precursors and novel analogs of netropsin

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