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1996 Journal Article Substrate docking algorithms and the predicition of substrate specificityDe Voss, James J. and Ortiz De Montellano, Paul R. (1996). Substrate docking algorithms and the predicition of substrate specificity. Methods in Enzymology, 272, 336-347. |
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1995 Journal Article Enhanced secretion of glycocholic acid in a specially adapted cell line is associated with overexpression of apparently novel ATP-binding cassette proteinsBrown Jr., R. S., Lomri, N., De Voss, J., Rahmaoui, C. M., Xie, M. H., Hua, T., Lidofsky, S. D. and Scharschmidt, B. F. (1995). Enhanced secretion of glycocholic acid in a specially adapted cell line is associated with overexpression of apparently novel ATP-binding cassette proteins. Proceedings of the National Academy of Sciences of the United States of America, 92 (12), 5421-5425. doi: 10.1073/pnas.92.12.5421 |
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1995 Journal Article Computer-Assisted, Structure-Based Prediction of Substrates for Cytochrome P450camDe Voss, James J. and Ortiz de Montellano, Paul R. (1995). Computer-Assisted, Structure-Based Prediction of Substrates for Cytochrome P450cam. Journal of the American Chemical Society, 117 (14), 4185-4186. doi: 10.1021/ja00119a041 |
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1994 Journal Article Nonpeptide HIV Protease Inhibitors. Differential Introduction of Alkylamino Groups into the Two Aryl Rings of HaloperidolLee, Kwan Hee, McPhee, Fiona, DeVoss, James J., Craik, Charles S. and de Montellano, Paul R. Ortiz (1994). Nonpeptide HIV Protease Inhibitors. Differential Introduction of Alkylamino Groups into the Two Aryl Rings of Haloperidol. Journal of Organic Chemistry, 59 (21), 6194-6199. doi: 10.1021/jo00100a021 |
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1994 Journal Article General Approach to the Synthesis of Specifically Deuterium-Labeled NucleosidesDe Voss, James J., Hangeland, Jon J. and Townsend, Craig A. (1994). General Approach to the Synthesis of Specifically Deuterium-Labeled Nucleosides. Journal of Organic Chemistry, 59 (10), 2715-2723. doi: 10.1021/jo00089a013 |
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1994 Journal Article In vitro characterization of nonpeptide irreversible inhibitors of HIV proteasesSalto, Rafael, Babé, Lilia M., Li, Jia, Rosé, Jason R., Yu, Zhonghua, Burlingame, Aima, De Voss, James J., Sui, Zhihua, Ortiz De Montellano, Paul and Craik, Charles S. (1994). In vitro characterization of nonpeptide irreversible inhibitors of HIV proteases. Journal of Biological Chemistry, 269 (14), 10691-10698. |
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1994 Journal Article Haloperidol-Based Irreversible Inhibitors of the HIV-1 and HIV-2 ProteasesDe Voss, James J., Sui, Zhihua, DeCamp, Dianne L., Salto, Rafael, Babé, Lilia M., Craik, Charles S. and de Montellano, Paul R. Ortiz (1994). Haloperidol-Based Irreversible Inhibitors of the HIV-1 and HIV-2 Proteases. Journal of Medicinal Chemistry, 37 (5), 665-673. doi: 10.1021/jm00031a017 |
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1994 Journal Article Synthesis of medium size rings containing oxygen and sulfur by ring expansion of halodioxolanes, dioxanes and oxathiolanesDe Voss, James J. and Sui, Zhihua (1994). Synthesis of medium size rings containing oxygen and sulfur by ring expansion of halodioxolanes, dioxanes and oxathiolanes. Tetrahedron Letters, 35 (1), 49-52. doi: 10.1016/0040-4039(94)88159-6 |
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1993 Journal Article Synthesis of haloperidol ethanedithioketal HIV-1 protease inhibitors: Magnesium chloride facilitated addition of Grignard reagentsSui, Z., De Voss, J. J., DeCamp, D. L., Li, J., Craik, C. S. and Ortiz De Montellano, P. R. (1993). Synthesis of haloperidol ethanedithioketal HIV-1 protease inhibitors: Magnesium chloride facilitated addition of Grignard reagents. Synthesis (8), 803-808. |
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1992 Journal Article Ring Expansion of Halo Dithiolanes and Dithianes: A Facile Synthesis of Medium-Ring DithiacycloalkenesSui, Zhihua, Furth, Paul S. and De Voss, James J. (1992). Ring Expansion of Halo Dithiolanes and Dithianes: A Facile Synthesis of Medium-Ring Dithiacycloalkenes. Journal of Organic Chemistry, 57 (24), 6658-6662. doi: 10.1021/jo00050a058 |
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1991 Journal Article Mercury(II)-mediated routes to some side-chain functionalised 1,7-dioxaspiro[5.5]undecanes. Applications of Luche-Barbier chemoselective addition to ketoaldehydesDevoss, JJ, Jamie, JF, Blanchfield, JT, Fletcher, MT, Oshea, MG and Kitching, W (1991). Mercury(II)-mediated routes to some side-chain functionalised 1,7-dioxaspiro[5.5]undecanes. Applications of Luche-Barbier chemoselective addition to ketoaldehydes. Tetrahedron, 47 (10-11), 1985-1996. doi: 10.1016/S0040-4020(01)96110-1 |
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1990 Journal Article Site-Specific Atom Transfer from DNA to a Bound Ligand Defines the Geometry of a DNA-Calicheamicin ϒ11 ComplexDe Voss, James J., Townsend, Craig A., Ding, Wei Dong, Morton, George O., Ellestad, George A., Zein, Nada, Tabor, Alethea B. and Schreiber, Stuart L. (1990). Site-Specific Atom Transfer from DNA to a Bound Ligand Defines the Geometry of a DNA-Calicheamicin ϒ11 Complex. Journal of the American Chemical Society, 112 (26), 9669-9670. doi: 10.1021/ja00182a053 |
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1990 Journal Article Characterization of the in vitro cyclization chemistry of calicheamicin and its relation to dna cleavageDe Voss, James J., Hangeland, Jon J. and Townsend, Craig A. (1990). Characterization of the in vitro cyclization chemistry of calicheamicin and its relation to dna cleavage. Journal of the American Chemical Society, 112 (11), 4554-4556. doi: 10.1021/ja00167a069 |
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1989 Journal Article 1‐Mesyl‐4‐[2‐(methoxycarbonyl)ethyl]‐3‐(methoxycarbonyl)methyl‐N,N‐dimethylpyrrole‐2‐carboxamideAllen, F. H., Battersby, A. R., De Voss, J. J., Doyle, M. J. and Raithby, P. R. (1989). 1‐Mesyl‐4‐[2‐(methoxycarbonyl)ethyl]‐3‐(methoxycarbonyl)methyl‐N,N‐dimethylpyrrole‐2‐carboxamide. Acta Crystallographica Section C, 45 (4), 692-694. doi: 10.1107/S0108270188012740 |
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1986 Journal Article Spiroacetals from dienones and hydroxyenones by mercury(II) cyclisationKitching, William, Lewis, Judith A., Fletcher, Mary T., De Voss, James J., Drew, Richard A.I. and Moore, Christopher J. (1986). Spiroacetals from dienones and hydroxyenones by mercury(II) cyclisation. Journal of the Chemical Society. Chemical Communications, 1986 (11), 855-856. doi: 10.1039/c39860000855 |
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1985 Journal Article The Diastereomeric 8, 9-Epoxides of Limonene (The 8, 9-Epoxy-p-menth-1-enes)Carman R.M., De Voss J.J. and Greenfield K.L. (1985). The Diastereomeric 8, 9-Epoxides of Limonene (The 8, 9-Epoxy-p-menth-1-enes). Australian Journal of Chemistry, 39 (3), 441-446. doi: 10.1071/CH9860441 |
