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25
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33751392005
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Preparation of Polyfunctional Nitro Olefins and Nitroalkanes Using the Copper-Zinc Reagents RCu-(CN)ZnI
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Jubert, C.; Knochel, P. Preparation of Polyfunctional Nitro Olefins and Nitroalkanes Using the Copper-Zinc Reagents RCu-(CN)ZnI. J. Org. Chem. 1992, 57, 5431-5438.
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Jubert, C.1
Knochel, P.2
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26
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0030974655
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Asymmetric Syntheses and Absolute Stereochemistry of 5,6-Dihydro-α-pyrones, a New Class of Potent HIV Protease Inhibitors
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Judge, T. M.; Phillips, G.; Morris, J. K.; Lovasz, K. D.; Romines, K. R.; Luke, G. P.; Tulinsky, J.; Tustin, J. M.; Chrusciel, R. A.; Dolak, L. A.; Mizsak, S. A.; Watt, W.; Morris, J.; Vander Velde, S. L.; Strohbach, J. W.; Gammill, R. B. Asymmetric Syntheses and Absolute Stereochemistry of 5,6-Dihydro-α-pyrones, A New Class of Potent HIV Protease Inhibitors. J. Am. Chem. Soc. 1997, 119, 3627-3628. Stereoselective pilot scale syntheses have also been developed (J. Org. Chem., in press).
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(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 3627-3628
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Judge, T.M.1
Phillips, G.2
Morris, J.K.3
Lovasz, K.D.4
Romines, K.R.5
Luke, G.P.6
Tulinsky, J.7
Tustin, J.M.8
Chrusciel, R.A.9
Dolak, L.A.10
Mizsak, S.A.11
Watt, W.12
Morris, J.13
Vander Velde, S.L.14
Strohbach, J.W.15
Gammill, R.B.16
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27
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0030974655
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Stereoselective pilot scale syntheses have also been developed
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in press
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Judge, T. M.; Phillips, G.; Morris, J. K.; Lovasz, K. D.; Romines, K. R.; Luke, G. P.; Tulinsky, J.; Tustin, J. M.; Chrusciel, R. A.; Dolak, L. A.; Mizsak, S. A.; Watt, W.; Morris, J.; Vander Velde, S. L.; Strohbach, J. W.; Gammill, R. B. Asymmetric Syntheses and Absolute Stereochemistry of 5,6-Dihydro-α-pyrones, A New Class of Potent HIV Protease Inhibitors. J. Am. Chem. Soc. 1997, 119, 3627-3628. Stereoselective pilot scale syntheses have also been developed (J. Org. Chem., in press).
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J. Org. Chem.
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28
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0029941361
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Structure-Based Design of Novel HIV Protease Inhibitors: Sulfonamide-Containing 4-Hydroxyeoumarins and 4-Hydroxy-2-pyrones as Potent Non-Peptidic Inhibitors
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Thaisrivongs, S.; Janakiraman, M. N.; Chong, K.-T.; Tomich, P. K.; Dolak, L. A.; Turner, S. R.; Strohbach, J. W.; Lynn, J. C.; Horng, M.-M.; Hinshaw, R. R.; Watenpaugh, K. D. Structure-Based Design of Novel HIV Protease Inhibitors: Sulfonamide-Containing 4-Hydroxyeoumarins and 4-Hydroxy-2-pyrones as Potent Non-Peptidic Inhibitors. J. Med. Chem. 1996, 39, 2400-2410.
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Thaisrivongs, S.1
Janakiraman, M.N.2
Chong, K.-T.3
Tomich, P.K.4
Dolak, L.A.5
Turner, S.R.6
Strohbach, J.W.7
Lynn, J.C.8
Horng, M.-M.9
Hinshaw, R.R.10
Watenpaugh, K.D.11
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29
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0025641617
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Stability and Activity of Human Immunodeficiency Virus Protease: Comparison of the Natural Dimer with a Homologous, Single-Chain Tethered Dimer
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Cheng, Y.-S. E.; Yin, F. H.; Foundling, S.; Blomstrom, D.; Kettner, C. A. Stability and Activity of Human Immunodeficiency Virus Protease: Comparison of the Natural Dimer with a Homologous, Single-Chain Tethered Dimer. Proc. Natl. Acad. Sci. U.S.A. 1990, 88, 9660-9664.
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Cheng, Y.-S.E.1
Yin, F.H.2
Foundling, S.3
Blomstrom, D.4
Kettner, C.A.5
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30
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0028105957
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The HIV-1 Protease as Enzyme and Substrate: Mutagenesis of Autolysis Sites and Generation of a Stable Mutant with Retained Kinetic Properties
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Mildner, A. M.; Rothrock, D. J.; Leone, J. W.; Bannow, C. A.; Lull, J. M.; Reardon, I. M.; Sarcich, J. L.; Howe, W. J.; Tomich, C. C.; Smith, C. W.; Heinrikson, R. L.; Tomasselli, A. G. The HIV-1 Protease as Enzyme and Substrate: Mutagenesis of Autolysis Sites and Generation of a Stable Mutant with Retained Kinetic Properties. Biochemistry 1994, 33, 9405-9413.
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(1994)
Biochemistry
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Mildner, A.M.1
Rothrock, D.J.2
Leone, J.W.3
Bannow, C.A.4
Lull, J.M.5
Reardon, I.M.6
Sarcich, J.L.7
Howe, W.J.8
Tomich, C.C.9
Smith, C.W.10
Heinrikson, R.L.11
Tomasselli, A.G.12
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31
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14444286877
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note
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We thank Professor Ben M. Dunn, University of Florida, Gainesville, FL, for the aspartyl protease assay results.
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32
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0028854676
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Selection and Analysis of Human Immunodeficiency Virus Type 1 Variants with Increased Resistance to ABT-538, a Novel Protease Inhibitor
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Markowitz, M.; Mo, H.; Kempf, D. J.; Norbeck, D. W.; Bhat, T. N.; Erickson, J. W.; Ho, D. D. Selection and Analysis of Human Immunodeficiency Virus Type 1 Variants with Increased Resistance to ABT-538, a Novel Protease Inhibitor. J. Virology 1995, 69, 701-706.
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(1995)
J. Virology
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Markowitz, M.1
Mo, H.2
Kempf, D.J.3
Norbeck, D.W.4
Bhat, T.N.5
Erickson, J.W.6
Ho, D.D.7
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33
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0030895692
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Antiviral Activity of the Dihydropyrone PNU-140690, a New Nonpeptidic Human Immunodeficienty Virus Protease Inhibitor
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Poppe, S. M.; Slade, D. E.; Chong, K.-T.; Hinshaw, R. R.; Pagano, P. J.; Markowitz, M.; Ho, D. D.; Mo, H.; Gorman, R. R., III; Dueweke, T. J.; Thaisrivongs, S.; Tarpley, W. G. Antiviral Activity of the Dihydropyrone PNU-140690, a New Nonpeptidic Human Immunodeficienty Virus Protease Inhibitor. Antimicrob. Agents Chemother. 1997, 41, 1058-1063.
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(1997)
Antimicrob. Agents Chemother.
, vol.41
, pp. 1058-1063
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Poppe, S.M.1
Slade, D.E.2
Chong, K.-T.3
Hinshaw, R.R.4
Pagano, P.J.5
Markowitz, M.6
Ho, D.D.7
Mo, H.8
Gorman III, R.R.9
Dueweke, T.J.10
Thaisrivongs, S.11
Tarpley, W.G.12
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34
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14444272684
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unpublished results
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Wathen, W. M. In vitro evaluation of U-140135 and U-140690 protease inhibitors against a panel of HIV-1 clinical isolates (contracted study with SRA Technologies), unpublished results; experiments performed according to the procedure of Japour, A. J.; Mayers, D. L.; Johnson, V. A.; Kuritzkes, D. R.; Beckett, L. A.; Arduino, J.-M.; Lane, J.; Black, R. J.; Reichelderfer, P. S.; D'Aquila, R. T.; Crumpacker, C. S. Standardized Peripheral Blood Mononuclear Cell Culture Assay for Determination of Drug Susceptibilities of Clinical Human Immunodeficiency Virus Type 1 Isolates. Antimicrob. Agents Chemother. 1993, 37, 1095-1101.
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Vitro Evaluation of U-140135 and U-140690 Protease Inhibitors Against a Panel of HIV-1 Clinical Isolates (Contracted Study with SRA Technologies)
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Wathen, W.M.1
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35
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0027270541
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Standardized Peripheral Blood Mononuclear Cell Culture Assay for Determination of Drug Susceptibilities of Clinical Human Immunodeficiency Virus Type 1 Isolates
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Wathen, W. M. In vitro evaluation of U-140135 and U-140690 protease inhibitors against a panel of HIV-1 clinical isolates (contracted study with SRA Technologies), unpublished results; experiments performed according to the procedure of Japour, A. J.; Mayers, D. L.; Johnson, V. A.; Kuritzkes, D. R.; Beckett, L. A.; Arduino, J.-M.; Lane, J.; Black, R. J.; Reichelderfer, P. S.; D'Aquila, R. T.; Crumpacker, C. S. Standardized Peripheral Blood Mononuclear Cell Culture Assay for Determination of Drug Susceptibilities of Clinical Human Immunodeficiency Virus Type 1 Isolates. Antimicrob. Agents Chemother. 1993, 37, 1095-1101.
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(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 1095-1101
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Japour, A.J.1
Mayers, D.L.2
Johnson, V.A.3
Kuritzkes, D.R.4
Beckett, L.A.5
Arduino, J.-M.6
Lane, J.7
Black, R.J.8
Reichelderfer, P.S.9
D'Aquila, R.T.10
Crumpacker, C.S.11
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36
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7844245269
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Single-dose safety, tolerance, and pharmacokinetics of PNU-140690, a new HIV protease inhibitor, in healthy volunteers
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Toronto, Ontario, Sept 28-Oct 1
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Borin, M. T.; Carlson, G. F.; Wang, Y.; Brewer, J. E.; Daenzer, C. L.; Baldwin, J. R.; Li, H. Single-dose safety, tolerance, and pharmacokinetics of PNU-140690, a new HIV protease inhibitor, in healthy volunteers. 37th ICACC, Toronto, Ontario, Sept 28-Oct 1, 1997.
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(1997)
37th ICACC
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Borin, M.T.1
Carlson, G.F.2
Wang, Y.3
Brewer, J.E.4
Daenzer, C.L.5
Baldwin, J.R.6
Li, H.7
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