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For example, amino acid phosphoramidate nucleosides: (a) Mcintee, E. J.; Wagner, C. R. Amino acid phosphoramidate nucleosides: Potential ADEPT/GDEPT substrates. Bioorg. Med. Chem. Lett. 2001, 11 (21), 2803-2805; (b) Chang, S. N.; Griesgraber, G.; Wagner, C. R. Comparison of the antiviral activity of hydrophobic amino acid phosphoramidate monoesters of 2′,3′- dideoxyadenosine (DDA) and 3′-azido-3′-deoxythymidine (AZT). Nucleosides Nucleotides 2001, 20 (8), 1571-1582; (c) Song, H.; Griesgraber, G. W.; Wagner, C. R.; Zimmerman, C. L. Pharmacokinetics of amino acid phosphoramidate monoesters of zidovudine in rats. Antimicrob. Agents Chemother. 2002, 46 (5), 1357-1363. Nucleoside with peptide or the derivative of amino acid as base segment: (d) Turner, J. J.; Filippov, D. V.; Overhand, M.; van der Marel, G. A.; van Boom, J. H. Synthesis of novel amino acid carbohydrate hybrids via Mitsunobu glycosylation of nitrobenzenesulfonamides. Tetrahedron Lett. 2001, 42 (13), 5763-5767; (e) Dewynter, G.; Aouf, N.; Regainia, Z.; Montera, J.-L. Synthesis of pseudonucleosides containing chiral sulfahydantoins as aglycone (II). Tetrahedron. 1996, 52 (3), 993-1004.
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Comparison of the antiviral activity of hydrophobic amino acid phosphoramidate monoesters of 2′,3′-dideoxyadenosine (DDA) and 3′-azido-3′-deoxythymidine (AZT)
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For example, amino acid phosphoramidate nucleosides: (a) Mcintee, E. J.; Wagner, C. R. Amino acid phosphoramidate nucleosides: Potential ADEPT/GDEPT substrates. Bioorg. Med. Chem. Lett. 2001, 11 (21), 2803-2805; (b) Chang, S. N.; Griesgraber, G.; Wagner, C. R. Comparison of the antiviral activity of hydrophobic amino acid phosphoramidate monoesters of 2′,3′- dideoxyadenosine (DDA) and 3′-azido-3′-deoxythymidine (AZT). Nucleosides Nucleotides 2001, 20 (8), 1571-1582; (c) Song, H.; Griesgraber, G. W.; Wagner, C. R.; Zimmerman, C. L. Pharmacokinetics of amino acid phosphoramidate monoesters of zidovudine in rats. Antimicrob. Agents Chemother. 2002, 46 (5), 1357-1363. Nucleoside with peptide or the derivative of amino acid as base segment: (d) Turner, J. J.; Filippov, D. V.; Overhand, M.; van der Marel, G. A.; van Boom, J. H. Synthesis of novel amino acid carbohydrate hybrids via Mitsunobu glycosylation of nitrobenzenesulfonamides. Tetrahedron Lett. 2001, 42 (13), 5763-5767; (e) Dewynter, G.; Aouf, N.; Regainia, Z.; Montera, J.-L. Synthesis of pseudonucleosides containing chiral sulfahydantoins as aglycone (II). Tetrahedron. 1996, 52 (3), 993-1004.
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Pharmacokinetics of amino acid phosphoramidate monoesters of zidovudine in rats
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For example, amino acid phosphoramidate nucleosides: (a) Mcintee, E. J.; Wagner, C. R. Amino acid phosphoramidate nucleosides: Potential ADEPT/GDEPT substrates. Bioorg. Med. Chem. Lett. 2001, 11 (21), 2803-2805; (b) Chang, S. N.; Griesgraber, G.; Wagner, C. R. Comparison of the antiviral activity of hydrophobic amino acid phosphoramidate monoesters of 2′,3′- dideoxyadenosine (DDA) and 3′-azido-3′-deoxythymidine (AZT). Nucleosides Nucleotides 2001, 20 (8), 1571-1582; (c) Song, H.; Griesgraber, G. W.; Wagner, C. R.; Zimmerman, C. L. Pharmacokinetics of amino acid phosphoramidate monoesters of zidovudine in rats. Antimicrob. Agents Chemother. 2002, 46 (5), 1357-1363. Nucleoside with peptide or the derivative of amino acid as base segment: (d) Turner, J. J.; Filippov, D. V.; Overhand, M.; van der Marel, G. A.; van Boom, J. H. Synthesis of novel amino acid carbohydrate hybrids via Mitsunobu glycosylation of nitrobenzenesulfonamides. Tetrahedron Lett. 2001, 42 (13), 5763-5767; (e) Dewynter, G.; Aouf, N.; Regainia, Z.; Montera, J.-L. Synthesis of pseudonucleosides containing chiral sulfahydantoins as aglycone (II). Tetrahedron. 1996, 52 (3), 993-1004.
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Song, H.1
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0035855256
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Synthesis of novel amino acid carbohydrate hybrids via Mitsunobu glycosylation of nitrobenzenesulfonamides
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For example, amino acid phosphoramidate nucleosides: (a) Mcintee, E. J.; Wagner, C. R. Amino acid phosphoramidate nucleosides: Potential ADEPT/GDEPT substrates. Bioorg. Med. Chem. Lett. 2001, 11 (21), 2803-2805; (b) Chang, S. N.; Griesgraber, G.; Wagner, C. R. Comparison of the antiviral activity of hydrophobic amino acid phosphoramidate monoesters of 2′,3′- dideoxyadenosine (DDA) and 3′-azido-3′-deoxythymidine (AZT). Nucleosides Nucleotides 2001, 20 (8), 1571-1582; (c) Song, H.; Griesgraber, G. W.; Wagner, C. R.; Zimmerman, C. L. Pharmacokinetics of amino acid phosphoramidate monoesters of zidovudine in rats. Antimicrob. Agents Chemother. 2002, 46 (5), 1357-1363. Nucleoside with peptide or the derivative of amino acid as base segment: (d) Turner, J. J.; Filippov, D. V.; Overhand, M.; van der Marel, G. A.; van Boom, J. H. Synthesis of novel amino acid carbohydrate hybrids via Mitsunobu glycosylation of nitrobenzenesulfonamides. Tetrahedron Lett. 2001, 42 (13), 5763-5767; (e) Dewynter, G.; Aouf, N.; Regainia, Z.; Montera, J.-L. Synthesis of pseudonucleosides containing chiral sulfahydantoins as aglycone (II). Tetrahedron. 1996, 52 (3), 993-1004.
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Synthesis of pseudonucleosides containing chiral sulfahydantoins as aglycone (II)
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For example, amino acid phosphoramidate nucleosides: (a) Mcintee, E. J.; Wagner, C. R. Amino acid phosphoramidate nucleosides: Potential ADEPT/GDEPT substrates. Bioorg. Med. Chem. Lett. 2001, 11 (21), 2803-2805; (b) Chang, S. N.; Griesgraber, G.; Wagner, C. R. Comparison of the antiviral activity of hydrophobic amino acid phosphoramidate monoesters of 2′,3′- dideoxyadenosine (DDA) and 3′-azido-3′-deoxythymidine (AZT). Nucleosides Nucleotides 2001, 20 (8), 1571-1582; (c) Song, H.; Griesgraber, G. W.; Wagner, C. R.; Zimmerman, C. L. Pharmacokinetics of amino acid phosphoramidate monoesters of zidovudine in rats. Antimicrob. Agents Chemother. 2002, 46 (5), 1357-1363. Nucleoside with peptide or the derivative of amino acid as base segment: (d) Turner, J. J.; Filippov, D. V.; Overhand, M.; van der Marel, G. A.; van Boom, J. H. Synthesis of novel amino acid carbohydrate hybrids via Mitsunobu glycosylation of nitrobenzenesulfonamides. Tetrahedron Lett. 2001, 42 (13), 5763-5767; (e) Dewynter, G.; Aouf, N.; Regainia, Z.; Montera, J.-L. Synthesis of pseudonucleosides containing chiral sulfahydantoins as aglycone (II). Tetrahedron. 1996, 52 (3), 993-1004.
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Synthesis of nucleosides XVII: Synthesis of 1-glycosyl-5-nitro imidazoles and pyrazoles
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An improved synthesis of α-AZA, α-AZP and α-AZG, the precursors to clinical markers of tissue hypoxia
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