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2006

Journal Article

Asparinins, asparosides, curillins, curillosides and shavatarins: structural clarification with the isolation of shatavarin V, a new steroidal saponin from the root of Asparagus racemosus

Hayes, P. Y., Jahidin, A. H., Lehmann, R., Penman, K., Kitching, W. and De Voss, J. J. (2006). Asparinins, asparosides, curillins, curillosides and shavatarins: structural clarification with the isolation of shatavarin V, a new steroidal saponin from the root of Asparagus racemosus. Tetrahedron Letters, 47 (-), 8683-8687. doi: 10.1016/j.tetlet.2006.10.030

Asparinins, asparosides, curillins, curillosides and shavatarins: structural clarification with the isolation of shatavarin V, a new steroidal saponin from the root of Asparagus racemosus

2006

Journal Article

Structural revision of shatavarins I and IV, the major components from the roots of Asparagus racemosus

Hayes, P. Y., Jahidin, A. H., Lehmann, R., Penman, K., Kitching, W. and De Voss, J. J. (2006). Structural revision of shatavarins I and IV, the major components from the roots of Asparagus racemosus. Tetrahedron Letters, 47 (39), 6965-6969. doi: 10.1016/j.tetlet.2006.07.121

Structural revision of shatavarins I and IV, the major components from the roots of Asparagus racemosus

2005

Journal Article

Cytochrome P450 enzyme-mediated degradation of Echinacea alkylamides in human liver microsomes

Matthias, A., Gillam, E. M. J., Penman, K. G., Matovic, N. J., Bone, K. M., De Voss, J. J. and Lehmann, R. P. (2005). Cytochrome P450 enzyme-mediated degradation of Echinacea alkylamides in human liver microsomes. Chemico-biological Interactions, 155 (1-2), 62-70. doi: 10.1016/j.cbi.2005.04.003

Cytochrome P450 enzyme-mediated degradation of Echinacea alkylamides in human liver microsomes

2005

Journal Article

Cyclopropyl containing fatty acids as mechanistic probes for cytochromes P450

Cryle, Max J., Ortiz de Montellano, Paul R. and De Voss, James J. (2005). Cyclopropyl containing fatty acids as mechanistic probes for cytochromes P450. Journal of Organic Chemistry, 70 (7), 2455-2469. doi: 10.1021/jo047985d

Cyclopropyl containing fatty acids as mechanistic probes for cytochromes P450

2005

Journal Article

Sodium paeoniflorin sulfonate, a process derived artefact from paeoniflorin

Hayes, P. Y. N., Lehmann, R. P., Penman, K. G., Kitching, W. and De Voss, J. J. (2005). Sodium paeoniflorin sulfonate, a process derived artefact from paeoniflorin. Tetrahedron Letters, 46 (15), 2615-2618. doi: 10.1016/j.tetlet.2005.02.082

Sodium paeoniflorin sulfonate, a process derived artefact from paeoniflorin

2005

Journal Article

Spiroacetal biosynthesis: ()-1,7-dioxaspiro[5.5]undecane in Bactrocera cacuminata and Bactrocera oleae (olive fruit fly)

Schwartz, B. D., McErlean, C. S. P., Fletcher, M. T., Mazomenos, B. E., Konstantopoulou, M. A., Kitching, W. and De Voss, J. J. (2005). Spiroacetal biosynthesis: ()-1,7-dioxaspiro[5.5]undecane in Bactrocera cacuminata and Bactrocera oleae (olive fruit fly). Organic Letters, 7 (6), 1173-1176. doi: 10.1021/ol050143w

Spiroacetal biosynthesis: ()-1,7-dioxaspiro[5.5]undecane in Bactrocera cacuminata and Bactrocera oleae (olive fruit fly)

2005

Journal Article

Calibration of the channel that determines the omega-hydroxylation regiospecificity of cytochrome P4504A1 - Catalytic oxidation of 12-halododecanoic acids

He, X., Cryle, M. J., De Voss, J. J. and de Montellano, P. R. O. (2005). Calibration of the channel that determines the omega-hydroxylation regiospecificity of cytochrome P4504A1 - Catalytic oxidation of 12-halododecanoic acids. Journal of Biological Chemistry, 280 (24), 22697-22705. doi: 10.1074/jbc.M502632200

Calibration of the channel that determines the omega-hydroxylation regiospecificity of cytochrome P4504A1 - Catalytic oxidation of 12-halododecanoic acids

2005

Journal Article

Flexible synthesis of enantiomerically pure 2,8-dialkyl-1,7-dioxaspiro[5.5]undecanes and 2,7-dialkyl-1,6-dioxaspiro[4.5]decanes from propargylic and homopropargylic alcohols

Schwartz, B. D., Hayes, P. Y. N., Kitching, W. and De Voss, J. J. (2005). Flexible synthesis of enantiomerically pure 2,8-dialkyl-1,7-dioxaspiro[5.5]undecanes and 2,7-dialkyl-1,6-dioxaspiro[4.5]decanes from propargylic and homopropargylic alcohols. Journal Of Organic Chemistry, 70 (8), 3054-3065. doi: 10.1021/jo0477547

Flexible synthesis of enantiomerically pure 2,8-dialkyl-1,7-dioxaspiro[5.5]undecanes and 2,7-dialkyl-1,6-dioxaspiro[4.5]decanes from propargylic and homopropargylic alcohols

2004

Journal Article

A precision apparatus, with solid phase micro-extraction monitoring capability, for incorporation studies of gaseous precursors into insect-derived metabolites

Fletcher, Mary T., Wood, Barry J., Schwartz, Brett D., Rahm, Fredrik, Lambert, Lynette K., Brereton, Ian M., Moore, Christopher J., De Voss, James J. and Kitching, William (2004). A precision apparatus, with solid phase micro-extraction monitoring capability, for incorporation studies of gaseous precursors into insect-derived metabolites. Arkivoc, 2004 (x), 109-117. doi: 10.3998/ark.5550190.0005.a12

A precision apparatus, with solid phase micro-extraction monitoring capability, for incorporation studies of gaseous precursors into insect-derived metabolites

2004

Journal Article

Cyclopropyl fatty acids implicate a radical but not a cation as an intermediate in P450(BM3)-catalysed hydroxylations

Cryle, Max J., Stuthe, Julia M. U., Ortiz de Montellano, Paul R. and De Voss, James J. (2004). Cyclopropyl fatty acids implicate a radical but not a cation as an intermediate in P450(BM3)-catalysed hydroxylations. Chemical Communications, 10 (5), 512-513. doi: 10.1039/b315911f

Cyclopropyl fatty acids implicate a radical but not a cation as an intermediate in P450(BM3)-catalysed hydroxylations

2004

Journal Article

Crystal structure of P450cin in a complex with its substrate, 1,8-cineole, a close structural homologue to D-camphor, the substrate for P450cam

Meharenna, Y. T., Li, H. Y., Hawkes, D. B., Pearson, A. G., De Voss, J. and Poulos, T. L. (2004). Crystal structure of P450cin in a complex with its substrate, 1,8-cineole, a close structural homologue to D-camphor, the substrate for P450cam. Biochemistry, 43 (29), 9487-9494. doi: 10.1021/bi049293p

Crystal structure of P450cin in a complex with its substrate, 1,8-cineole, a close structural homologue to D-camphor, the substrate for P450cam

2004

Journal Article

Assessment of arginine 97 and lysine 72 as determinants of substrate specificity in cytochrome P450 2C9 (CYP2C9)

Davies, C., Witham, K., Scott, J. R., Pearson, A., De Voss, J. J., Graham, S. E. and Gillam, E. M. J. (2004). Assessment of arginine 97 and lysine 72 as determinants of substrate specificity in cytochrome P450 2C9 (CYP2C9). Drug Metabolism and Disposition, 32 (4), 431-436. doi: 10.1124/dmd.32.4.431

Assessment of arginine 97 and lysine 72 as determinants of substrate specificity in cytochrome P450 2C9 (CYP2C9)

2004

Journal Article

Carbon-carbon bond cleavage by cytochrome P450Biol (CYP107H1)

Cryle, Max J. and De Voss, James J. (2004). Carbon-carbon bond cleavage by cytochrome P450Biol (CYP107H1). Chemical Communications, 2004 (1), 86-87. doi: 10.1039/b311652b

Carbon-carbon bond cleavage by cytochrome P450Biol (CYP107H1)

2004

Journal Article

Permeability studies of alkylamides and caffeic acid conjugates from echinacea using a Caco-2 cell monolayer model

Matthias, A., Blanchfield, J. T., Penman, K. G., Toth, I., Lang, C. S., De Voss, J. J. and Lehmann, R. P. (2004). Permeability studies of alkylamides and caffeic acid conjugates from echinacea using a Caco-2 cell monolayer model. Journal of Clinical Pharmacy And Therapeutics, 29 (1), 7-13. doi: 10.1046/j.1365-2710.2003.00530.x

Permeability studies of alkylamides and caffeic acid conjugates from echinacea using a Caco-2 cell monolayer model

2003

Journal Article

Insect chemistry and chirality

Hayes, Patricia Y., Fletcher, Mary T., Chow, Sharon, McGrath, Matthew J., Tu, Yong Q., Zhang, Hesheng, Hungerford, Natasha L., McErlean, Christopher S. P., Stok, Jeannette E., Moore, Christopher J., De Voss, James J. and Kitching, William (2003). Insect chemistry and chirality. Chirality, 15 (S1), S116-S127. doi: 10.1002/chir.10273

Insect chemistry and chirality

2003

Journal Article

Electrochemistry of P450cin: new insights into P450 electron transfer

Aguey-Zinsou, Kondo-François, Bernhardt, Paul V., De Voss, James J. and Slessor, Kate E. (2003). Electrochemistry of P450cin: new insights into P450 electron transfer. Chemical Communications, 3 (3), 418-419. doi: 10.1039/b211567k

Electrochemistry of P450cin: new insights into P450 electron transfer

2003

Journal Article

Reactions catalyzed by bacterial cytochromes P450

Cryle, M. J., Stok, J. E. and De Voss, J. J. (2003). Reactions catalyzed by bacterial cytochromes P450. Australian Journal of Chemistry, 56 (8), 749-762. doi: 10.1071/CH03040

Reactions catalyzed by bacterial cytochromes P450

2003

Journal Article

Products of Cytochrome P450BioI (CYP107H1)-Catalyzed Oxidation of Fatty Acids

Cryle, M. J., Matovic, N. J. and De Voss, J. J. (2003). Products of Cytochrome P450BioI (CYP107H1)-Catalyzed Oxidation of Fatty Acids. Organic Letters, 5 (18), 3341-3344. doi: 10.1021/ol035254e

Products of Cytochrome P450BioI (CYP107H1)-Catalyzed Oxidation of Fatty Acids

2002

Journal Article

[18O]-Oxygen incorporation reveals novel pathways in spiroacetal biosynthesis by Bactrocera cacuminata and B. cucumis

Fletcher, Mary T., Wood, Barry J., Brereton, Ian M., Stok, Jeanette E., De Voss, James J. and Kitching, William (2002). [18O]-Oxygen incorporation reveals novel pathways in spiroacetal biosynthesis by Bactrocera cacuminata and B. cucumis. Journal of the American Chemical Society, 124 (26), 7666-7667. doi: 10.1021/ja026215l

[18O]-Oxygen incorporation reveals novel pathways in spiroacetal biosynthesis by Bactrocera cacuminata and B. cucumis

2002

Journal Article

Medium ring ethers by ring expansion-ring contraction: Synthesis of lauthisan

Coster, M. J. and De Voss, J. J. (2002). Medium ring ethers by ring expansion-ring contraction: Synthesis of lauthisan. Organic Letters, 4 (18), 3047-3050. doi: 10.1021/ol0262946

Medium ring ethers by ring expansion-ring contraction: Synthesis of lauthisan