Publications
2022
Coupling Novel Probes with Molecular Localization Microscopy Reveals Cell Wall Homeostatic Mechanisms in <i>Staphylococcus aureus</i>
Lund, V. A., Gangotra, H., Zhao, Z., Sutton, J. A. F., Wacnik, K., DeMeester, K., . . . Foster, S. J. (2022). Coupling Novel Probes with Molecular Localization Microscopy Reveals Cell Wall Homeostatic Mechanisms in <i>Staphylococcus aureus</i>. ACS CHEMICAL BIOLOGY, 17(12), 3298-3305. doi:10.1021/acschembio.2c00741
2021
Current applications of kinetic resolution in the asymmetric synthesis of substituted pyrrolidines
Berry, S. S., & Jones, S. (2021). Current applications of kinetic resolution in the asymmetric synthesis of substituted pyrrolidines. ORGANIC & BIOMOLECULAR CHEMISTRY, 19(48), 10493-10515. doi:10.1039/d1ob01943k
2020
Spatial organization of <i>Clostridium difficile</i> S-layer biogenesis
Oatley, P., Kirk, J. A., Ma, S., Jones, S., & Fagan, R. P. (2020). Spatial organization of <i>Clostridium difficile</i> S-layer biogenesis. SCIENTIFIC REPORTS, 10(1). doi:10.1038/s41598-020-71059-x
Evaluation of the anti-inflammatory effects of synthesised tanshinone I and isotanshinone I analogues in zebrafish
Foulkes, M. J., Tolliday, F. H., Henry, K. M., Renshaw, S. A., & Jones, S. (2020). Evaluation of the anti-inflammatory effects of synthesised tanshinone I and isotanshinone I analogues in zebrafish. PLOS ONE, 15(10). doi:10.1371/journal.pone.0240231
2019
Evaluation of bifunctional chiral phosphine oxide catalysts for the asymmetric hydrosilylation of ketimines
Warner, C. J. A., Berry, S. S., & Jones, S. (2019). Evaluation of bifunctional chiral phosphine oxide catalysts for the asymmetric hydrosilylation of ketimines. TETRAHEDRON, 75(50). doi:10.1016/j.tet.2019.130733
Evaluation of the anti-inflammatory effects of synthesised tanshinone I and isotanshinone I analogues in zebrafish
Synergistic substrate and catalyst effects in the addition of trimethylsilyl cyanide to imines derived from lactic acid
Fields, A. M., & Jones, S. (2019). Synergistic substrate and catalyst effects in the addition of trimethylsilyl cyanide to imines derived from lactic acid. TETRAHEDRON, 75(25), 3413-3420. doi:10.1016/j.tet.2019.04.067
2018
Spatial organization of <i>Clostridium difficile</i> S-layer biogenesis
Molecular coordination of <i>Staphylococcus aureus</i> cell division
Lund, V. A., Wacnik, K., Turner, R. D., Cotterell, B. E., Walther, C. G., Fenn, S. J., . . . Foster, S. J. (2018). Molecular coordination of <i>Staphylococcus aureus</i> cell division. ELIFE, 7. doi:10.7554/eLife.32057
2017
Direct arterial injection of hyperpolarized <SUP>13</SUP>C-labeled substrates into rat tumors for rapid MR detection of metabolism with minimal substrate dilution
Reynolds, S., Metcalf, S., Cochrane, E. J., Collins, R. C., Jones, S., Paley, M. N. J., & Tozer, G. M. (2017). Direct arterial injection of hyperpolarized <SUP>13</SUP>C-labeled substrates into rat tumors for rapid MR detection of metabolism with minimal substrate dilution. MAGNETIC RESONANCE IN MEDICINE, 78(6), 2116-2126. doi:10.1002/mrm.26628
The Synthesis and Photophysical Analysis of a Series of 4-Nitrobenzochalcogenadiazoles for Super-Resolution Microscopy
Jenkinson, D. R., Cadby, A. J., & Jones, S. (2017). The Synthesis and Photophysical Analysis of a Series of 4-Nitrobenzochalcogenadiazoles for Super-Resolution Microscopy. CHEMISTRY-A EUROPEAN JOURNAL, 23(51), 12585-12592. doi:10.1002/chem.201702289
Expression and regulation of drug transporters in vertebrate neutrophils
Foulkes, M. J., Henry, K. M., Rougeot, J., Hooper-Greenhill, E., Loynes, C. A., Jeffrey, P., . . . Renshaw, S. A. (2017). Expression and regulation of drug transporters in vertebrate neutrophils. SCIENTIFIC REPORTS, 7. doi:10.1038/s41598-017-04785-4
Mechanistic investigations of the asymmetric hydrosilylation of ketimines with trichlorosilane reveals a dual activation model and an organocatalyst with enhanced efficiency
Li, X., Reeder, A. T., Torri, F., Adams, H., & Jones, S. (2017). Mechanistic investigations of the asymmetric hydrosilylation of ketimines with trichlorosilane reveals a dual activation model and an organocatalyst with enhanced efficiency. ORGANIC & BIOMOLECULAR CHEMISTRY, 15(11), 2422-2435. doi:10.1039/c6ob02537d
2016
Identification of benzopyrone as a common structural feature in compounds with anti-inflammatory activity in a zebrafish phenotypic screen
Robertson, A. L., Ogryzko, N. V., Henry, K. M., Loynes, C. A., Foulkes, M. J., Meloni, M. M., . . . Renshaw, S. A. (2016). Identification of benzopyrone as a common structural feature in compounds with anti-inflammatory activity in a zebrafish phenotypic screen. DISEASE MODELS & MECHANISMS, 9(6), 621-632. doi:10.1242/dmm.024935
ChemInform Abstract: Enantioselective Desymmetrization of Glutarimides Catalyzed by Oxazaborolidines Derived from cis‐1‐Amino‐indan‐2‐ol.
Kutama, I. U., & Jones, S. (2016). ChemInform Abstract: Enantioselective Desymmetrization of Glutarimides Catalyzed by Oxazaborolidines Derived from cis‐1‐Amino‐indan‐2‐ol.. ChemInform, 47(15). doi:10.1002/chin.201615147
<i>P</i>-Chiral phosphine oxide catalysed reduction of prochiral ketimines using trichlorosilane
Warner, C. J. A., Reeder, A. T., & Jones, S. (2016). <i>P</i>-Chiral phosphine oxide catalysed reduction of prochiral ketimines using trichlorosilane. TETRAHEDRON-ASYMMETRY, 27(2-3), 136-141. doi:10.1016/j.tetasy.2016.01.001
Synthesis of [3-<SUP>13</SUP>C]-2,3-dihydroxy-4-methoxybenzaldehyde
Collins, R. C., Paley, M. N., Tozer, G. M., & Jones, S. (2016). Synthesis of [3-<SUP>13</SUP>C]-2,3-dihydroxy-4-methoxybenzaldehyde. TETRAHEDRON LETTERS, 57(5), 563-565. doi:10.1016/j.tetlet.2015.12.088
2015
Enantioselective Desymmetrization of Glutarimides Catalyzed by Oxazaborolidines Derived from <i>cis</i>-1-Amino-indan-2-ol
Kutama, I. U., & Jones, S. (2015). Enantioselective Desymmetrization of Glutarimides Catalyzed by Oxazaborolidines Derived from <i>cis</i>-1-Amino-indan-2-ol. JOURNAL OF ORGANIC CHEMISTRY, 80(22), 11468-11479. doi:10.1021/acs.joc.5b02177
Evaluating hydrogen bonding control in the diastereoselective Diels-Alder reactions of 9-(2-aminoethyl)-anthracene derivatives
Bawa, R. A., Gautier, F. -M., Adams, H., Meijer, A. J. H. M., & Jones, S. (2015). Evaluating hydrogen bonding control in the diastereoselective Diels-Alder reactions of 9-(2-aminoethyl)-anthracene derivatives. ORGANIC & BIOMOLECULAR CHEMISTRY, 13(42), 10569-10577. doi:10.1039/c5ob01343g
2014
Examining the origin of selectivity in the reaction of racemic alcohols with chiral <i>N</i>-phosphoryl oxazolidinones
Crook, S., Parr, N. J., Simmons, J., & Jones, S. (2014). Examining the origin of selectivity in the reaction of racemic alcohols with chiral <i>N</i>-phosphoryl oxazolidinones. TETRAHEDRON-ASYMMETRY, 25(18-19), 1298-1308. doi:10.1016/j.tetasy.2014.08.003
ChemInform Abstract: Evaluating Dynamic Kinetic Resolution Strategies in the Asymmetric Hydrosilylation of Cyclic Ketimines.
Jones, S., & Zhao, P. (2014). ChemInform Abstract: Evaluating Dynamic Kinetic Resolution Strategies in the Asymmetric Hydrosilylation of Cyclic Ketimines.. ChemInform, 45(29). doi:10.1002/chin.201429110
Enantioselective Catalytic Desymmetrization of Maleimides by Temporary Removal of an Internal Mirror Plane and Stereoablative Over-reduction: Synthesis of (<i>R</i>)-Pyrrolam A
Marsh, B. J., Adams, H., Barker, M. D., Kutama, I. U., & Jones, S. (2014). Enantioselective Catalytic Desymmetrization of Maleimides by Temporary Removal of an Internal Mirror Plane and Stereoablative Over-reduction: Synthesis of (<i>R</i>)-Pyrrolam A. ORGANIC LETTERS, 16(14), 3780-3783. doi:10.1021/ol5016702
Bactericidal Activity of the Human Skin Fatty Acid <i>cis</i>-6-Hexadecanoic Acid on <i>Staphylococcus aureus</i>
Cartron, M. L., England, S. R., Chiriac, A. I., Josten, M., Turner, R., Rauter, Y., . . . Foster, S. J. (2014). Bactericidal Activity of the Human Skin Fatty Acid <i>cis</i>-6-Hexadecanoic Acid on <i>Staphylococcus aureus</i>. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 58(7), 3599-3609. doi:10.1128/AAC.01043-13
A Zebrafish Compound Screen Reveals Modulation of Neutrophil Reverse Migration as an Anti-Inflammatory Mechanism
Robertson, A. L., Holmes, G. R., Bojarczuk, A. N., Burgon, J., Loynes, C. A., Chimen, M., . . . Renshaw, S. A. (2014). A Zebrafish Compound Screen Reveals Modulation of Neutrophil Reverse Migration as an Anti-Inflammatory Mechanism. SCIENCE TRANSLATIONAL MEDICINE, 6(225). doi:10.1126/scitranslmed.3007672
Evaluating dynamic kinetic resolution strategies in the asymmetric hydrosilylation of cyclic ketimines
Jones, S., & Zhao, P. (2014). Evaluating dynamic kinetic resolution strategies in the asymmetric hydrosilylation of cyclic ketimines. TETRAHEDRON-ASYMMETRY, 25(3), 238-244. doi:10.1016/j.tetasy.2013.11.006
Synthesis of an azabicyclic framework towards (±)-actinophyllic acid
Mortimer, D., Whiting, M., Harrity, J. P. A., Jones, S., & Coldham, I. (2014). Synthesis of an azabicyclic framework towards (±)-actinophyllic acid. TETRAHEDRON LETTERS, 55(6), 1255-1257. doi:10.1016/j.tetlet.2014.01.019
2012
ChemInform Abstract: Synthesis of Chiral β‐Amino Acid Derivatives by Asymmetric Hydrosilylation with an Imidazole Derived Organocatalyst.
Jones, S., & Li, X. (2012). ChemInform Abstract: Synthesis of Chiral β‐Amino Acid Derivatives by Asymmetric Hydrosilylation with an Imidazole Derived Organocatalyst.. ChemInform, 43(48). doi:10.1002/chin.201248061
ChemInform Abstract: Trichlorosilane‐Mediated Asymmetric Reductions of the C=N Bond
Jones, S., & Warner, C. J. A. (2012). ChemInform Abstract: Trichlorosilane‐Mediated Asymmetric Reductions of the C=N Bond. ChemInform, 43(29). doi:10.1002/chin.201229258
Synthesis of chiral β-amino acid derivatives by asymmetric hydrosilylation with an imidazole derived organocatalyst
Jones, S., & Li, X. (2012). Synthesis of chiral β-amino acid derivatives by asymmetric hydrosilylation with an imidazole derived organocatalyst. TETRAHEDRON, 68(27-28), 5522-5532. doi:10.1016/j.tet.2012.04.084
ChemInform Abstract: Scope of the Organocatalyzed Asymmetric Reductive Amination of Ketones with Trichlorosilane.
Gautier, F., Jones, S., Li, X., & Martin, S. J. (2012). ChemInform Abstract: Scope of the Organocatalyzed Asymmetric Reductive Amination of Ketones with Trichlorosilane.. ChemInform, 43(15). doi:10.1002/chin.201215054
Trichlorosilane mediated asymmetric reductions of the C=N bond
Jones, S., & Warner, C. J. A. (2012). Trichlorosilane mediated asymmetric reductions of the C=N bond. ORGANIC & BIOMOLECULAR CHEMISTRY, 10(11), 2189-2200. doi:10.1039/c2ob06854k
Enantioselective preparation of <i>P</i>-chiral phosphine oxide organocatalysts and their application in asymmetric synthesis
Warner, C. J. A., & Jones, S. (2012). Enantioselective preparation of <i>P</i>-chiral phosphine oxide organocatalysts and their application in asymmetric synthesis. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 243. Retrieved from https://www.webofscience.com/
2011
Enantioselective Preparation of <i>P</i>-Chiral Phosphine Oxides
Adams, H., Collins, R. C., Jones, S., & Warner, C. J. A. (2011). Enantioselective Preparation of <i>P</i>-Chiral Phosphine Oxides. ORGANIC LETTERS, 13(24), 6576-6579. doi:10.1021/ol202916j
Scope of the organocatalysed asymmetric reductive amination of ketones with trichlorosilane
Gautier, F. -M., Jones, S., Li, X., & Martin, S. J. (2011). Scope of the organocatalysed asymmetric reductive amination of ketones with trichlorosilane. ORGANIC & BIOMOLECULAR CHEMISTRY, 9(22), 7860-7868. doi:10.1039/c1ob05965c
Diels-Alder reactions and transformations of 2-cyclopenten-1-one with a chiral anthracene template
Adams, H., Jones, S., Meijer, A. J. H. M., Najah, Z., Ojea-Jimenez, I., & Reeder, A. T. (2011). Diels-Alder reactions and transformations of 2-cyclopenten-1-one with a chiral anthracene template. TETRAHEDRON-ASYMMETRY, 22(16-17), 1620-1625. doi:10.1016/j.tetasy.2011.09.002
Synthesis of quaternary stereogenic centres <i>via</i> stereoselective intermolecular Friedel-Crafts reactions
Ball, J. C., Gleave, R., & Jones, S. (2011). Synthesis of quaternary stereogenic centres <i>via</i> stereoselective intermolecular Friedel-Crafts reactions. ORGANIC & BIOMOLECULAR CHEMISTRY, 9(11), 4353-4360. doi:10.1039/c1ob05129f
A tandem asymmetric synthesis approach for the efficient preparation of enantiomerically pure 9-(hydroxyethyl) anthracene
Ball, J. C., Brennan, P., Elsunaki, T. M., Jaunet, A., & Jones, S. (2011). A tandem asymmetric synthesis approach for the efficient preparation of enantiomerically pure 9-(hydroxyethyl) anthracene. TETRAHEDRON-ASYMMETRY, 22(3), 253-255. doi:10.1016/j.tetasy.2011.01.019
2010
Evaluating the use of chiral anthracene templates to access pyroglutamic acids
Hasbullah, S. A., & Jones, S. (2010). Evaluating the use of chiral anthracene templates to access pyroglutamic acids. TETRAHEDRON-ASYMMETRY, 21(21-22), 2719-2725. doi:10.1016/j.tetasy.2010.10.021
Diastereoselective Cycloadditions and Transformations of <i>N</i>-Alkyl and <i>N</i>-Aryl Maleimides with Chiral 9-Anthrylethanol Derivatives
Adams, H., Elsunaki, T. M., Ojea-Jimenez, I., Jones, S., & Meijer, A. J. H. M. (2010). Diastereoselective Cycloadditions and Transformations of <i>N</i>-Alkyl and <i>N</i>-Aryl Maleimides with Chiral 9-Anthrylethanol Derivatives. JOURNAL OF ORGANIC CHEMISTRY, 75(18), 6252-6262. doi:10.1021/jo101437b
ChemInform Abstract: Enantioselective Synthesis of Allylic Alcohols via an Oxazaborolidinium Ion Catalyzed Diels—Alder/retro‐Diels—Alder Sequence.
Jones, S., & Valette, D. (2010). ChemInform Abstract: Enantioselective Synthesis of Allylic Alcohols via an Oxazaborolidinium Ion Catalyzed Diels—Alder/retro‐Diels—Alder Sequence.. ChemInform, 41(13). doi:10.1002/chin.201013031
Phase Transformations of Glutamic Acid and Its Decomposition Products
Wu, H., Reeves-McLaren, N., Jones, S., Ristic, R. I., Fairclough, J. P. A., & West, A. R. (2010). Phase Transformations of Glutamic Acid and Its Decomposition Products. CRYSTAL GROWTH & DESIGN, 10(2), 988-994. doi:10.1021/cg901303a
ChemInform Abstract: The Dienolate Aldol Reaction of (E)‐N‐Crotonoyl C(4)‐Isopropyl SuperQuat: Asymmetric Synthesis of α‐Vinyl‐β‐hydroxycarboxylic Acid Derivatives and Conversion to α‐Ethylidene‐β‐hydroxyesters (β‐Substituted Baylis—Hillman Products).
Davies, S. G., Elend, D. L., Jones, S., Roberts, P. M., Savory, E. D., Smith, A. D., & Thomson, J. E. (2010). ChemInform Abstract: The Dienolate Aldol Reaction of (E)‐N‐Crotonoyl C(4)‐Isopropyl SuperQuat: Asymmetric Synthesis of α‐Vinyl‐β‐hydroxycarboxylic Acid Derivatives and Conversion to α‐Ethylidene‐β‐hydroxyesters (β‐Substituted Baylis—Hillman Products).. ChemInform, 41(2). doi:10.1002/chin.201002058
2009
Scope and limitations of the Minisci reaction for the synthesis of aza-heterocycles
Burgin, R. N., Jones, S., & Tarbit, B. (2009). Scope and limitations of the Minisci reaction for the synthesis of aza-heterocycles. TETRAHEDRON LETTERS, 50(49), 6772-6774. doi:10.1016/j.tetlet.2009.09.112
Enantioselective Synthesis of Allylic Alcohols via an Oxazaborolidinium Ion Catalyzed Diels-Alder/Retro-Diels-Alder Sequence
Jones, S., & Valette, D. (2009). Enantioselective Synthesis of Allylic Alcohols via an Oxazaborolidinium Ion Catalyzed Diels-Alder/Retro-Diels-Alder Sequence. ORGANIC LETTERS, 11(22), 5358-5361. doi:10.1021/ol902280d
The dienolate aldol reaction of (<i>E</i>)-<i>N</i>-crotonoyl C(4)-isopropyl SuperQuat: asymmetric synthesis of α-vinyl-β-hydroxycarboxylic acid derivatives and conversion to α-ethylidene-β-hydroxyesters (β-substituted Baylis-Hillman products)
Davies, S. G., Elend, D. L., Jones, S., Roberts, P. M., Savory, E. D., Smith, A. D., & Thomson, J. E. (2009). The dienolate aldol reaction of (<i>E</i>)-<i>N</i>-crotonoyl C(4)-isopropyl SuperQuat: asymmetric synthesis of α-vinyl-β-hydroxycarboxylic acid derivatives and conversion to α-ethylidene-β-hydroxyesters (β-substituted Baylis-Hillman products). TETRAHEDRON, 65(37), 7837-7851. doi:10.1016/j.tet.2009.07.004
ChemInform Abstract: Asymmetric Reduction of Ketimines with Trichlorosilane Employing an Imidazole Derived Organocatalyst.
Gautier, F., Jones, S., & Martin, S. J. (2009). ChemInform Abstract: Asymmetric Reduction of Ketimines with Trichlorosilane Employing an Imidazole Derived Organocatalyst.. ChemInform, 40(24). doi:10.1002/chin.200924054
Asymmetric reduction of ketimines with trichlorosilane employing an imidazole derived organocatalyst
Gautier, F. -M., Jones, S., & Martin, S. J. (2009). Asymmetric reduction of ketimines with trichlorosilane employing an imidazole derived organocatalyst. ORGANIC & BIOMOLECULAR CHEMISTRY, 7(2), 229-231. doi:10.1039/b816051a
ORGN 110-Stereoselective cycloadditions of cyclopentenone with anthracene derivatives and subsequent asymmetric transformations
Jones, S., & Najah, Z. (2009). ORGN 110-Stereoselective cycloadditions of cyclopentenone with anthracene derivatives and subsequent asymmetric transformations. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 237. Retrieved from https://www.webofscience.com/
2008
ChemInform Abstract: Kinetic Resolution of Racemic Pyrrolidine‐2,5‐diones Using Chiral Oxazaborolidine Catalysts.
Barker, M. D., Dixon, R. A., Jones, S., & Marsh, B. J. (2008). ChemInform Abstract: Kinetic Resolution of Racemic Pyrrolidine‐2,5‐diones Using Chiral Oxazaborolidine Catalysts.. ChemInform, 39(37). doi:10.1002/chin.200837104
ChemInform Abstract: Asymmetric Synthesis of Corsifuran A by an Enantioselective Oxazaborolidine Reduction.
Adams, H., Gilmore, N. J., Jones, S., Muldowney, M. P., von Reuss, S. H., & Vemula, R. (2008). ChemInform Abstract: Asymmetric Synthesis of Corsifuran A by an Enantioselective Oxazaborolidine Reduction.. ChemInform, 39(35). doi:10.1002/chin.200835195
Lysophospholipid metabolism facilitates Toll-like receptor 4 membrane translocation to regulate the inflammatory response
Jackson, S. K., Abate, W., Parton, J., Jones, S., & Harwood, J. L. (2008). Lysophospholipid metabolism facilitates Toll-like receptor 4 membrane translocation to regulate the inflammatory response. JOURNAL OF LEUKOCYTE BIOLOGY, 84(1), 86-92. doi:10.1189/jlb.0907601
Kinetic resolution of racemic pyrrolidine-2,5-diones using chiral oxazaborolidine catalysts
Barker, M. D., Dixon, R. A., Jones, S., & Marsh, B. J. (2008). Kinetic resolution of racemic pyrrolidine-2,5-diones using chiral oxazaborolidine catalysts. CHEMICAL COMMUNICATIONS, (19), 2218-2220. doi:10.1039/b800510a
Asymmetric synthesis of corsifuran a by an enantioselective oxazaborolidine reduction
Adams, H., Gilmore, N. J., Jones, S., Muldowney, M. P., von Reuss, S. H., & Vemula, R. (2008). Asymmetric synthesis of corsifuran a by an enantioselective oxazaborolidine reduction. ORGANIC LETTERS, 10(7), 1457-1460. doi:10.1021/ol800239q
ORGN 47-Synthesis and application of N-phosphoryl oxazolidinones to asymmetric phosphorylation
Jones, S., & Crook, S. (2008). ORGN 47-Synthesis and application of N-phosphoryl oxazolidinones to asymmetric phosphorylation. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 236. Retrieved from https://www.webofscience.com/
2007
Asymmetric control in Diels-Alder cycloadditions of chiral 9-aminoanthracenes by relay of stereochemical information
Adams, H., Bawa, R. A., McMillan, K. G., & Jones, S. (2007). Asymmetric control in Diels-Alder cycloadditions of chiral 9-aminoanthracenes by relay of stereochemical information. TETRAHEDRON-ASYMMETRY, 18(8), 1003-1012. doi:10.1016/j.tetasy.2007.04.012
The Crucial Role of the Nitrogen Substituent in the Desymmetrization of Cyclic meso‐Imides Using B‐Me and B‐O‐Me Oxazaborolidine Catalysts.
Barker, M. D., Dixon, R. A., Jones, S., & Marsh, B. J. (2007). The Crucial Role of the Nitrogen Substituent in the Desymmetrization of Cyclic meso‐Imides Using B‐Me and B‐O‐Me Oxazaborolidine Catalysts.. ChemInform, 38(12). doi:10.1002/chin.200712122
ORGN 579-Approaches to the asymmetric synthesis of chiral amines
Gautier, F., Jones, S., & Martin, S. (2007). ORGN 579-Approaches to the asymmetric synthesis of chiral amines. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 234. Retrieved from https://www.webofscience.com/
ORGN 638-Use of chiral anthracene templates for the synthesis of cyclohexene monoepoxide natural products
Jaunet, A., Jones, S., & Poinsard, C. (2007). ORGN 638-Use of chiral anthracene templates for the synthesis of cyclohexene monoepoxide natural products. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 234. Retrieved from https://www.webofscience.com/
ORGN 752-Construction of the quinoline ring system by application of minisci radical cyclization
Burgin, R. N., Jones, S., Smith, A., & Tarbit, B. (2007). ORGN 752-Construction of the quinoline ring system by application of minisci radical cyclization. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 234. Retrieved from https://www.webofscience.com/
2006
The crucial role of the nitrogen substituent in the desymmetrisation of cyclic meso-imides using <i>B</i>-Me and <i>B</i>-OMe oxazaborolidine catalysts
Barker, M. D., Dixon, R. A., Jones, S., & Marsh, B. J. (2006). The crucial role of the nitrogen substituent in the desymmetrisation of cyclic meso-imides using <i>B</i>-Me and <i>B</i>-OMe oxazaborolidine catalysts. TETRAHEDRON, 62(50), 11663-11669. doi:10.1016/j.tet.2006.09.051
<i>N</i>-alkyl oxazolidines as stereocontrol elements in asymmetric Diels-Alder cycloadditions of 9-substituted anthracene derivatives
Adams, H., Bawa, R. A., & Jones, S. (2006). <i>N</i>-alkyl oxazolidines as stereocontrol elements in asymmetric Diels-Alder cycloadditions of 9-substituted anthracene derivatives. ORGANIC & BIOMOLECULAR CHEMISTRY, 4(22), 4206-4213. doi:10.1039/b610055d
Synthesis of Substituted 3‐Furan‐2(5H)‐ones via an Anthracene Diels—Alder Sequence.
Jones, S., & Wilson, I. (2006). Synthesis of Substituted 3‐Furan‐2(5H)‐ones via an Anthracene Diels—Alder Sequence.. ChemInform, 37(40). doi:10.1002/chin.200640097
Highly diastereoselective Diels-Alder cycloadditions of 9<i>R</i>-(1-methoxyethyl)anthracene with <i>p</i>-benzoquinone
Adams, H., Jones, S., & Ojea-Jimenez, I. (2006). Highly diastereoselective Diels-Alder cycloadditions of 9<i>R</i>-(1-methoxyethyl)anthracene with <i>p</i>-benzoquinone. ORGANIC & BIOMOLECULAR CHEMISTRY, 4(11), 2296-2303. doi:10.1039/b603819k
Synthesis of substituted 3-furan-2(5<i>H</i>)-ones via an anthracene Diels-Alder sequence
Jones, S., & Wilson, I. (2006). Synthesis of substituted 3-furan-2(5<i>H</i>)-ones via an anthracene Diels-Alder sequence. TETRAHEDRON LETTERS, 47(26), 4377-4380. doi:10.1016/j.tetlet.2006.04.097
ORGN 121-The effect of the nitrogen substituent on enantioselectivity of the catalytic asymmetric reduction of meso-imides with chiral oxazaborolidine catalysts
Jones, S., & Marsh, B. (2006). ORGN 121-The effect of the nitrogen substituent on enantioselectivity of the catalytic asymmetric reduction of meso-imides with chiral oxazaborolidine catalysts. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 232. Retrieved from https://www.webofscience.com/
2005
Catalytic Phosphorylation Using a Bifunctional Imidazole Derived Nucleophilic Catalyst.
Jones, S., Northen, J., & Rolfe, A. (2005). Catalytic Phosphorylation Using a Bifunctional Imidazole Derived Nucleophilic Catalyst.. ChemInform, 36(50). doi:10.1002/chin.200550161
Phosphorylation of Alcohols with N‐Phosphoryl Oxazolidinones Employing Copper(II) Triflate Catalysis.
Jones, S., & Smanmoo, C. (2005). Phosphorylation of Alcohols with N‐Phosphoryl Oxazolidinones Employing Copper(II) Triflate Catalysis.. ChemInform, 36(47). doi:10.1002/chin.200547049
Stereochemical consequences of the use of chiral <i>N</i>-phosphoryl oxazolidinones in the attempted kinetic resolution of bromomagnesium alkoxides
Jones, S., & Selitsianos, D. (2005). Stereochemical consequences of the use of chiral <i>N</i>-phosphoryl oxazolidinones in the attempted kinetic resolution of bromomagnesium alkoxides. TETRAHEDRON-ASYMMETRY, 16(18), 3128-3138. doi:10.1016/j.tetasy.2005.08.025
Catalytic phosphorylation using a bifunctional imidazole derived nucleophilic catalyst
Jones, S., Northen, J., & Rolfe, A. (2005). Catalytic phosphorylation using a bifunctional imidazole derived nucleophilic catalyst. CHEMICAL COMMUNICATIONS, (30), 3832-3834. doi:10.1039/b506344b
Phosphorylation of alcohols with <i>N</i>-phosphoryl oxazolidinones employing copper(II) triflate catalysis
Jones, S., & Smanmoo, C. (2005). Phosphorylation of alcohols with <i>N</i>-phosphoryl oxazolidinones employing copper(II) triflate catalysis. ORGANIC LETTERS, 7(15), 3271-3274. doi:10.1021/ol051104n
<i>catena</i>-Poly[[[tetrakis(dimethylformamide-κ<i>O</i>)-magnesium(II)]-μ-diphenylphosphato-κ<SUP>2</SUP><i>O</i>:<i>O′</i>]trifluoromethanesulfonate]
Adams, H., Rolfe, A., & Jones, S. (2005). <i>catena</i>-Poly[[[tetrakis(dimethylformamide-κ<i>O</i>)-magnesium(II)]-μ-diphenylphosphato-κ<SUP>2</SUP><i>O</i>:<i>O′</i>]trifluoromethanesulfonate]. ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 61, M1251-M1252. doi:10.1107/S1600536805016880
Chiral nucleophilic podand catalysts for asymmetric phosphoryl transfer.
Rolfe, A., & Jones, S. (2005). Chiral nucleophilic podand catalysts for asymmetric phosphoryl transfer.. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 229 (pp. U547-U548). Retrieved from https://www.webofscience.com/
Diastereoselective Diels-Alder reactions of polyether based chiral 9-substituted anthracenes
Jones, S., & Ojea-Jimenez, I. (2005). Diastereoselective Diels-Alder reactions of polyether based chiral 9-substituted anthracenes. POLYCYCLIC AROMATIC COMPOUNDS, 25(1), 1-12. doi:10.1080/10406630490461646
2004
Synthetic Applicability and in situ Recycling of a B‐Methoxy Oxazaborolidine Catalyst Derived from cis‐1‐Amino‐indan‐2‐ol.
Gilmore, N. J., Jones, S., & Muldowney, M. P. (2004). Synthetic Applicability and in situ Recycling of a B‐Methoxy Oxazaborolidine Catalyst Derived from cis‐1‐Amino‐indan‐2‐ol.. ChemInform, 35(48). doi:10.1002/chin.200448027
Phosphine Incorporation and Exchange in Mononuclear η<sup>5</sup>‐Cyclopentadienyl Iron Carbonyl Complexes
Davies, S. G., Jones, S., & Smith, A. D. (2004). Phosphine Incorporation and Exchange in Mononuclear η<sup>5</sup>‐Cyclopentadienyl Iron Carbonyl Complexes. ChemInform, 35(43). doi:10.1002/chin.200443243
Synthetic applicability and <i>in situ</i> recycling of a <i>B</i>-methoxy oxazaborolidne catalyst derived from cis-1-amino-indan-2-ol
Gilmore, N. J., Jones, S., & Muldowney, M. P. (2004). Synthetic applicability and <i>in situ</i> recycling of a <i>B</i>-methoxy oxazaborolidne catalyst derived from cis-1-amino-indan-2-ol. ORGANIC LETTERS, 6(16), 2805-2808. doi:10.1021/ol048916o
Ring Opening Reactions of N‐Alkyl Oxazolidinones with Organolithium Reagents.
Jones, S., & Norton, H. C. (2004). Ring Opening Reactions of N‐Alkyl Oxazolidinones with Organolithium Reagents.. ChemInform, 35(25). doi:10.1002/chin.200425142
N‐Phosphoryl Oxazolidinones as Effective Phosphorylating Agents.
Jones, S., & Smanmoo, C. (2004). N‐Phosphoryl Oxazolidinones as Effective Phosphorylating Agents.. ChemInform, 35(21). doi:10.1002/chin.200421161
The Diels-Aider adduct of <i>p</i>-benzoquinone and anthracene:: 9,10-tetrahydro-9,10[1′,2′]-benzenoanthracene-1′,4′(2′<i>H</i>,3′<i>H</i>)-dione
Adams, H., Ojea-Jimenez, I., & Jones, S. (2004). The Diels-Aider adduct of <i>p</i>-benzoquinone and anthracene:: 9,10-tetrahydro-9,10[1′,2′]-benzenoanthracene-1′,4′(2′<i>H</i>,3′<i>H</i>)-dione. ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 60, O690-O691. doi:10.1107/S160053680400707X
Synthesis and Diels-Alder reactions of 9-(4-benzyloxazolin-2-yl) anthracene
Bawa, R. A., & Jones, S. (2004). Synthesis and Diels-Alder reactions of 9-(4-benzyloxazolin-2-yl) anthracene. TETRAHEDRON, 60(12), 2765-2770. doi:10.1016/j.tet.2004.01.070
Diels—Alder Reactions of Anthracene, 9‐Substituted Anthracenes and 9,10‐Disubstituted Anthracenes
Atherton, J. C. C., & Jones, S. (2004). Diels—Alder Reactions of Anthracene, 9‐Substituted Anthracenes and 9,10‐Disubstituted Anthracenes. ChemInform, 35(7). doi:10.1002/chin.200407288
<i>N</i>-Phosphoryl oxazolidinones as effective phosphorylating agents
Jones, S., & Smanmoo, C. (2004). <i>N</i>-Phosphoryl oxazolidinones as effective phosphorylating agents. TETRAHEDRON LETTERS, 45(8), 1585-1588. doi:10.1016/j.tetlet.2004.01.003
Asymmetric catalysis utilising imidazoles
Norton, H. C., & Jones, S. (2004). Asymmetric catalysis utilising imidazoles. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 227 (pp. U181). Retrieved from https://www.webofscience.com/
Asymmetric reduction with aminoindanol based oxazaborolidines
Gilmore, N. J., & Jones, S. (2004). Asymmetric reduction with aminoindanol based oxazaborolidines. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 227 (pp. U181). Retrieved from https://www.webofscience.com/
Methods for chemical asymmetric phosphoryl transfer.
Jones, S., Rolfe, A., & Wilson, I. (2004). Methods for chemical asymmetric phosphoryl transfer.. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 227 (pp. U202). Retrieved from https://www.webofscience.com/
Ring opening reactions of N-alkyl oxazolidinones with organolithium reagents
Jones, S., & Norton, H. C. (2004). Ring opening reactions of N-alkyl oxazolidinones with organolithium reagents. SYNLETT, (2), 338-340. doi:10.1055/s-2003-44972
2003
Diels-Alder reactions of anthracene, 9-substituted anthracenes and 9,10-disubstituted anthracenes
Atherton, J. C. C., & Jones, S. (2003). Diels-Alder reactions of anthracene, 9-substituted anthracenes and 9,10-disubstituted anthracenes. TETRAHEDRON, 59(46), 9039-9057. doi:10.1016/j.tet.2003.09.014
An Improved Method for Lewis Acid Catalyzed Phosphoryl Transfer with Ti(t‐BuO)<sub>4</sub>.
Jones, S., Selitsianos, D., Thompson, K. J., & Toms, S. M. (2003). An Improved Method for Lewis Acid Catalyzed Phosphoryl Transfer with Ti(t‐BuO)<sub>4</sub>.. ChemInform, 34(42). doi:10.1002/chin.200342177
Evaluating the role of solvent and borane on the enantioselectivity of the oxazaborolidine reduction of prochiral ketones using catalysts derived from cis-(1<i>R</i>,2<i>S</i>)-1-amino-indan-2-ol
Gilmore, N. J., & Jones, S. (2003). Evaluating the role of solvent and borane on the enantioselectivity of the oxazaborolidine reduction of prochiral ketones using catalysts derived from cis-(1<i>R</i>,2<i>S</i>)-1-amino-indan-2-ol. TETRAHEDRON-ASYMMETRY, 14(15), 2115-2118. doi:10.1016/S0957-4166(03)00401-4
An improved method for Lewis acid catalyzed phosphoryl transfer with Ti(<i>t</i>-BuO)<sub>4</sub>
Jones, S., Selitsianos, D., Thompson, K. J., & Toms, S. M. (2003). An improved method for Lewis acid catalyzed phosphoryl transfer with Ti(<i>t</i>-BuO)<sub>4</sub>. JOURNAL OF ORGANIC CHEMISTRY, 68(13), 5211-5216. doi:10.1021/jo034331g
A Simple and Effective Method for Phosphoryl Transfer Using TiCl<sub>4</sub> Catalysis.
Jones, S., & Selitsianos, D. (2003). A Simple and Effective Method for Phosphoryl Transfer Using TiCl<sub>4</sub> Catalysis.. ChemInform, 34(10). doi:10.1002/chin.200310173
The [2,3] Sigmatropic Rearrangement of N‐Benzyl‐O‐allylhydroxylamines.
Davies, S. G., Fox, J. F., Jones, S., Price, A. J., Sanz, M. A., Sellers, T. G. R., . . . Teixeira, F. C. (2003). The [2,3] Sigmatropic Rearrangement of N‐Benzyl‐O‐allylhydroxylamines.. ChemInform, 34(2). doi:10.1002/chin.200302072
2002
Stoichiometric asymmetric processes
Jones, S. (2002). Stoichiometric asymmetric processes. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, (1), 1-21. doi:10.1039/b009236n
Establishing cleavage conditions for an anthracene chiral auxiliary using a photochemical retro Diels-Alder reaction
Atherton, J. C. C., & Jones, S. (2002). Establishing cleavage conditions for an anthracene chiral auxiliary using a photochemical retro Diels-Alder reaction. TETRAHEDRON LETTERS, 43(50), 9097-9100. doi:10.1016/S0040-4039(02)02255-4
A simple and effective method for phosphoryl transfer using TiCl<sub>4</sub> catalysis
Jones, S., & Selitsianos, D. (2002). A simple and effective method for phosphoryl transfer using TiCl<sub>4</sub> catalysis. ORGANIC LETTERS, 4(21), 3671-3673. doi:10.1021/ol026618q
The [2,3] sigmatropic rearrangement of <i>N</i>-benzyl-<i>O</i>-allylhydroxylamines
Davies, S. G., Fox, J. F., Jones, S., Price, A. J., Sanz, M. A., Sellers, T. G. R., . . . Teixeira, F. C. (2002). The [2,3] sigmatropic rearrangement of <i>N</i>-benzyl-<i>O</i>-allylhydroxylamines. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, (15), 1757-1765. doi:10.1039/b205323n
Efficient desymmetrisation of a <i>meso</i>-imide using a chiral oxazaborolidine catalyst
Dixon, R. A., & Jones, S. (2002). Efficient desymmetrisation of a <i>meso</i>-imide using a chiral oxazaborolidine catalyst. TETRAHEDRON-ASYMMETRY, 13(10), 1115-1119. doi:10.1016/S0957-4166(02)00248-3
ChemInform Abstract: Stoichiometric Asymmetric Processes
Jones, S. (2002). ChemInform Abstract: Stoichiometric Asymmetric Processes. ChemInform, 33(19). doi:10.1002/chin.200219252
ChemInform Abstract: Diastereomeric Control of Photoinduced Diels—Alder Reactions of 1‐Anthracen‐9‐yl‐ethanol by Hydrogen‐Bonding Effects.
Atherton, J. C. C., & Jones, S. (2002). ChemInform Abstract: Diastereomeric Control of Photoinduced Diels—Alder Reactions of 1‐Anthracen‐9‐yl‐ethanol by Hydrogen‐Bonding Effects.. ChemInform, 33(7). doi:10.1002/chin.200207100
Asymmetric reduction of amides and <i>meso</i>-imides using chiral oxazaborolidine catalysts.
Jones, S., & Dixon, R. A. (2002). Asymmetric reduction of amides and <i>meso</i>-imides using chiral oxazaborolidine catalysts.. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 224 (pp. U202). Retrieved from https://www.webofscience.com/
Diastereoselective [2,3]-sigmatropic rearrangements of lithium <i>N</i>-benzyl-<i>O</i>-allylhydroxylamides bearing a stereogenic centre adjacent to the migration terminus
Bull, S. D., Davies, S. G., Domíngez, S. H., Jones, S., Price, A. J., Sellers, T. G. R., & Smith, A. D. (2002). Diastereoselective [2,3]-sigmatropic rearrangements of lithium <i>N</i>-benzyl-<i>O</i>-allylhydroxylamides bearing a stereogenic centre adjacent to the migration terminus. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, (19), 2141-2150. doi:10.1039/b207069n
Mechanistic investigations in diastereoselective Diels-Alder additions of chiral 9-anthrylethanol derivatives
Atherton, J. C. C., & Jones, S. (2002). Mechanistic investigations in diastereoselective Diels-Alder additions of chiral 9-anthrylethanol derivatives. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, (19), 2166-2173. doi:10.1039/b206523a
Photoactivated chiral auxiliaries based upon functionalised anthracene derivatives.
Jones, S. (2002). Photoactivated chiral auxiliaries based upon functionalised anthracene derivatives.. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 224 (pp. U250-U251). Retrieved from https://www.webofscience.com/
Studies towards the synthesis of the potent antibiotic agent sarcophytolide.
Jones, S., & Toms, S. M. (2002). Studies towards the synthesis of the potent antibiotic agent sarcophytolide.. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 224 (pp. U201). Retrieved from https://www.webofscience.com/
2001
ChemInform Abstract: An Improved Procedure for the Preparation of 9,10‐Dibromoanthracene.
Jones, S., & Atherton, J. C. C. (2001). ChemInform Abstract: An Improved Procedure for the Preparation of 9,10‐Dibromoanthracene.. ChemInform, 32(47). doi:10.1002/chin.200147081
Diastereomeric control of photoinduced Diels-Alder reactions of 1-anthracen-9-yl-ethanol by hydrogen-bonding effects
Atherton, J. C. C., & Jones, S. (2001). Diastereomeric control of photoinduced Diels-Alder reactions of 1-anthracen-9-yl-ethanol by hydrogen-bonding effects. TETRAHEDRON LETTERS, 42(46), 8239-8241. doi:10.1016/S0040-4039(01)01742-7
Highly diastereoselective photochemical Diels-Alder reactions: towards the development of a photoactivated chiral auxiliary
Jones, S., & Atherton, J. C. C. (2001). Highly diastereoselective photochemical Diels-Alder reactions: towards the development of a photoactivated chiral auxiliary. TETRAHEDRON-ASYMMETRY, 12(8), 1117-1119. doi:10.1016/S0957-4166(01)00203-8
An improved procedure for the preparation of 9,10-dibromoanthracene
Jones, S., & Atherton, J. C. C. (2001). An improved procedure for the preparation of 9,10-dibromoanthracene. SYNTHETIC COMMUNICATIONS, 31(12), 1799-1802. doi:10.1081/SCC-100104326
2000
Asymmetric reduction using <i>N</i>-methyl and <i>N</i>-benzyl oxazaborolidines based upon <i>cis</i>-1-amino-2-indanol:: a preliminary mechanistic study
Jones, S., & Atherton, J. C. C. (2000). Asymmetric reduction using <i>N</i>-methyl and <i>N</i>-benzyl oxazaborolidines based upon <i>cis</i>-1-amino-2-indanol:: a preliminary mechanistic study. TETRAHEDRON-ASYMMETRY, 11(22), 4543-4548. doi:10.1016/S0957-4166(00)00422-5
Dimethyl 9,10-anthracenedicarboxylate:: a centrosymmetric <i>transoid</i> molecule
Jones, S., Atherton, J. C. C., Elsegood, M. R. J., & Clegg, W. (2000). Dimethyl 9,10-anthracenedicarboxylate:: a centrosymmetric <i>transoid</i> molecule. ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 56, 881-883. doi:10.1107/S0108270100004972
ChemInform Abstract: A Highly Diastereoselective [2,3]‐Sigmatropic N,O Rearrangement.
Bull, S. D., Davies, S. G., Jones, S., Ouzman, J. V. A., Price, A. J., & Watkin, D. J. (2000). ChemInform Abstract: A Highly Diastereoselective [2,3]‐Sigmatropic N,O Rearrangement.. ChemInform, 31(6). doi:10.1002/chin.200006048
1999
ChemInform Abstract: Asymmetric Alkylations Using SuperQuat Auxiliaries — An Investigation into the Synthesis and Stability of Enolates Derived from 5,5‐Disubstituted Oxazolidin‐2‐ones.
Bull, S. D., Davies, S. G., Jones, S., & Sanganee, H. J. (1999). ChemInform Abstract: Asymmetric Alkylations Using SuperQuat Auxiliaries — An Investigation into the Synthesis and Stability of Enolates Derived from 5,5‐Disubstituted Oxazolidin‐2‐ones.. ChemInform, 30(28). doi:10.1002/chin.199928028
ChemInform Abstract: A Novel [2,3] Intramolecular Rearrangement of N‐Benzyl‐O‐allylhydroxylamines.
DAVIES, S. G., JONES, S., SANZ, M. A., TEIXEIRA, F. C., & FOX, J. F. (1999). ChemInform Abstract: A Novel [2,3] Intramolecular Rearrangement of N‐Benzyl‐O‐allylhydroxylamines.. ChemInform, 30(5). doi:10.1002/chin.199905053
A highly diastereoselective [2,3]-sigmatropic N,O rearrangement
Bull, S. D., Davies, S. G., Jones, S., Ouzman, J. V. A., Price, A. J., & Watkin, D. J. (1999). A highly diastereoselective [2,3]-sigmatropic N,O rearrangement. CHEMICAL COMMUNICATIONS, (20), 2079-2080. doi:10.1039/a905981d
Asymmetric alkylations using SuperQuat auxiliaries - an investigation into the synthesis and stability of enolates derived from 5,5-disubstituted oxazolidin-2-ones
Bull, S. D., Davies, S. G., Jones, S., & Sanganee, H. J. (1999). Asymmetric alkylations using SuperQuat auxiliaries - an investigation into the synthesis and stability of enolates derived from 5,5-disubstituted oxazolidin-2-ones. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, (4), 387-398. doi:10.1039/a809715a
Phosphine photolabilisation studies of (η<SUP>5</SUP>-C<sub>5</sub>H<sub>5</sub>)Fe(PPH<sub>3</sub>)(CO)-COR (R = Me, Ph, 2,6-C<sub>6</sub>B<sub>3</sub>F<sub>2</sub>) and (η<SUP>5</SUP>-C<sub>5</sub>Me<sub>5</sub>)Fe(PPh<sub>3</sub>)(CO)-COR (R = Me, 2,6-C<sub>6</sub>H<sub>3</sub>F<sub>2</sub>) utilising NMR, laser desorption FT ICR MS and photofragmentation voltammetry analysis
Aplin, R. T., Booth, J., Compton, R. G., Davies, S. G., Jones, S., McNally, J. P., . . . Watkins, W. C. (1999). Phosphine photolabilisation studies of (η<SUP>5</SUP>-C<sub>5</sub>H<sub>5</sub>)Fe(PPH<sub>3</sub>)(CO)-COR (R = Me, Ph, 2,6-C<sub>6</sub>B<sub>3</sub>F<sub>2</sub>) and (η<SUP>5</SUP>-C<sub>5</sub>Me<sub>5</sub>)Fe(PPh<sub>3</sub>)(CO)-COR (R = Me, 2,6-C<sub>6</sub>H<sub>3</sub>F<sub>2</sub>) utilising NMR, laser desorption FT ICR MS and photofragmentation voltammetry analysis. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, (5), 913-922. doi:10.1039/a900207c
1998
ChemInform Abstract: A Practical Procedure for the Multigram Synthesis of the SuperQuat Chiral Auxiliaries.
BULL, S. D., DAVIES, S. G., JONES, S., POLYWKA, M. E. C., PRASAD, R. S., & SANGANEE, H. J. (1998). ChemInform Abstract: A Practical Procedure for the Multigram Synthesis of the SuperQuat Chiral Auxiliaries.. ChemInform, 29(33). doi:10.1002/chin.199833166
A practical procedure for the multigram synthesis of the SuperQuat chiral auxiliaries
Bull, S. D., Davies, S. G., Jones, S., Polywka, M. E. C., Prasad, R. S., & Sanganee, H. J. (1998). A practical procedure for the multigram synthesis of the SuperQuat chiral auxiliaries. SYNLETT, (5), 519-+. Retrieved from https://www.webofscience.com/
A novel [2,3] intramolecular rearrangement of <i>N</i>-benzyl-<i>O</i>-allylhydroxylamines
Davies, S. G., Jones, S., Sanz, M. A., Teixeira, F. C., & Fox, J. F. (1998). A novel [2,3] intramolecular rearrangement of <i>N</i>-benzyl-<i>O</i>-allylhydroxylamines. CHEMICAL COMMUNICATIONS, (20), 2235-2236. doi:10.1039/a806200e
Photoinduced configurational instability at iron in the aminocarbene complexes [(η<SUP>5</SUP>-C<sub>5</sub>H<sub>5</sub>)Fe(CO)(L){=C(NHR<SUP>2</SUP>)(CH<sub>2</sub>R<SUP>1</SUP>)}]<SUP>+</SUP>BF<sub>4</sub><SUP>-</SUP>
Davies, S. G., Jones, S., Metzler, M. R., Yanada, K., & Yanada, R. (1998). Photoinduced configurational instability at iron in the aminocarbene complexes [(η<SUP>5</SUP>-C<sub>5</sub>H<sub>5</sub>)Fe(CO)(L){=C(NHR<SUP>2</SUP>)(CH<sub>2</sub>R<SUP>1</SUP>)}]<SUP>+</SUP>BF<sub>4</sub><SUP>-</SUP>. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, (5), 1147-1152. doi:10.1039/a800937f
Synthesis and characterisation of the aminocarbene complexes [(η<SUP>5</SUP>-C<sub>5</sub>H<sub>5</sub>)Fe(CO)(PPh<sub>3</sub>){=C(NHR<SUP>2</SUP>)(CH<sub>2</sub>R<SUP>1</SUP>)}]<SUP>+</SUP>BF<sub>4</sub><SUP>-</SUP> [R<SUP>1</SUP> = H, Me or Pr; R<SUP>2</SUP> = H, Me, Et, CHMe<sub>2</sub>, CH<sub>2</sub>Ph, CH(Me)Ph, CH<sub>2</sub>CH=CH<sub>2</sub> or CH<sub>2</sub>CH<sub>2</sub>OH]
Davies, S. G., Edwards, A. J., Jones, S., Metzler, M. R., Yanada, K., & Yanada, R. (1998). Synthesis and characterisation of the aminocarbene complexes [(η<SUP>5</SUP>-C<sub>5</sub>H<sub>5</sub>)Fe(CO)(PPh<sub>3</sub>){=C(NHR<SUP>2</SUP>)(CH<sub>2</sub>R<SUP>1</SUP>)}]<SUP>+</SUP>BF<sub>4</sub><SUP>-</SUP> [R<SUP>1</SUP> = H, Me or Pr; R<SUP>2</SUP> = H, Me, Et, CHMe<sub>2</sub>, CH<sub>2</sub>Ph, CH(Me)Ph, CH<sub>2</sub>CH=CH<sub>2</sub> or CH<sub>2</sub>CH<sub>2</sub>OH]. JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, (10), 1587-1594. doi:10.1039/a800927i
1997
The addition of nitric oxide to 1,5-dimethylhexa-2,4-diene; X-ray crystal structure determination of the major product, (E)-2,5-dimethyl-2,5-dinitrohex-3-ene
Kelly, D. R., Jones, S., Adigun, J. O., Koh, K. S. V., Hibbs, D. E., Hursthouse, M. B., & Jackson, S. K. (1997). The addition of nitric oxide to 1,5-dimethylhexa-2,4-diene; X-ray crystal structure determination of the major product, (E)-2,5-dimethyl-2,5-dinitrohex-3-ene. TETRAHEDRON, 53(50), 17221-17234. doi:10.1016/S0040-4020(97)10202-2
ChemInform Abstract: The Addition of Nitric Oxide to 2,5‐Dimethyl‐hexa‐2,4‐diene Gives Nitrogen Dioxide Adducts.
KELLY, D. R., JONES, S., ADIGUN, J. O., KOH, K. S. V., & JACKSON, S. K. (1997). ChemInform Abstract: The Addition of Nitric Oxide to 2,5‐Dimethyl‐hexa‐2,4‐diene Gives Nitrogen Dioxide Adducts.. ChemInform, 28(23). doi:10.1002/chin.199723082
The addition of nitric oxide to 2,5-dimethyl-hexa-2,4-diene gives nitrogen dioxide adducts
Kelly, D. R., Jones, S., Adigun, J. O., Koh, K. S. V., & Jackson, S. K. (1997). The addition of nitric oxide to 2,5-dimethyl-hexa-2,4-diene gives nitrogen dioxide adducts. TETRAHEDRON LETTERS, 38(7), 1245-1248. doi:10.1016/S0040-4039(97)00048-8
ChemInform Abstract: NMR, MS and X‐Ray Crystal Structure Determination of the Bixin Family of Apocarotenoids.
KELLY, D. R., EDWARDS, A. A., PARKINSON, J. A., OLOVSSON, G., TROTTER, J., JONES, S., . . . HIBBS, D. E. (1997). ChemInform Abstract: NMR, MS and X‐Ray Crystal Structure Determination of the Bixin Family of Apocarotenoids.. ChemInform, 28(5). doi:10.1002/chin.199705211
1996
NMR, MS and X-ray crystal structure determination of the bixin family of apocarotenoids
Kelly, D. R., Edwards, A. A., Parkinson, J. A., Olovsson, G., Trotter, J., Jones, S., . . . Hibbs, D. E. (1996). NMR, MS and X-ray crystal structure determination of the bixin family of apocarotenoids. JOURNAL OF CHEMICAL RESEARCH, (10), 446-+. Retrieved from https://www.webofscience.com/
1995
<i>N</i>,<i>N</i>′-Bis(phenylmethylene)-1,2-Ethanediamine
Jones, S., & Burgin, R. (n.d.). <i>N</i>,<i>N</i>′-Bis(phenylmethylene)-1,2-Ethanediamine. John Wiley & Sons, Ltd. doi:10.1002/047084289x.rn00792
The synthesis and biological activity of analogues of 1,7-dioxaspiro-[5.5]undecane. The pheromone of the olive fly (Bactrocera oleae)
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