研究领域
Organic Chemistry
My group’s research is split roughly evenly between natural product synthesis and synthetic methodology development. Uniting these two strands is a desire to discover new molecular transformations and gain a deeper understanding of reactivity and selectivity.
近期论文
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V A Pal'chikov, J Robertson, Russ. J. Org. Chem. 2014, 50, 1369 [Zh. Org. Khim. 2014, 50, 1384]
Efficient Procedure for the Preparation of 2-Bromo-5-ethylfuran and its Unexpected Isomerization
W P Unsworth, N Clark, T O Ronson, K Stevens, A L Thompson, S G Lamont, J Robertson, Chem. Commun. 2014, 50, 11393
Rhodium(II)-Catalysed Tandem Aziridination and Ring-opening: Stereoselective Synthesis of Functionalised Tetrahydrofurans
J Robertson and K Stevens, Nat. Prod. Rep. 2014, 31, 1721
Pyrrolizidine Alkaloids
W P Unsworth, S G Lamont, J Robertson, Tetrahedron 2014, 70, 7388
Substrate Scope and Stereocontrol in the Rh(II)-Catalysed Oxyamination of Allylic Carbamates
K Y Seah, S J Macnaughton, J W P Dallimore, J Robertson, Org. Lett. 2014, 16, 884
Synthesis of Pandamarilactone-1
B Wu, G C Feast, A L Thompson, J Robertson, J. Org. Chem. 2012, 77, 10623
Synthesis of Stereoisomers of Artemisia and Chrysanthemum Bis(acetylenic) Enol Ether Spiroacetals
K Clarke, K Tchabanenko, R Pawlowsky, E Carter, M T King, K Musa-Veloso, M Ho, A Roberts, J Robertson, T B VanItallie, R L Veech, Regul. Toxicol. Pharmacol. 2012, 63, 401
Kinetics, Safety and Tolerability of (R)-3-Hydroxybutyl (R)-3-Hydroxybutyrate in Healthy Adult Subjects
K Clarke, K Tchabanenko, R Pawlowsky, E Carter, N S Knight, A J Murray, L E Cochlin, M T King, A W Wong, A Roberts, J Robertson, R L Veech, Regul. Toxicol. Pharmacol. 2012, 63, 196
Oral 28-Day and Developmental Toxicity Studies of (R)-3-Hydroxybutyl (R)-3-Hydroxybutyrate
O Zhurakovskyi and J Robertson, Abstr. Pap. Am. Chem. Soc. 2012, 243, 578-ORGN
Pericyclic Rearrangements of Tethered Allene Azides [abstract]
S Naud, S J Macnaughton, B S Dyson, D J Woollaston, J W P Dallimore, J Robertson, Org. Biomol. Chem. 2012, 10, 3506
Conformational Preferences of Oxy‐ Substituents in Butenolide‐tetrahydropyran Spiroacetals and Butenolide‐piperidine Spiro‐N,O‐acetals
K Stevens, A J Tyrrell, S Skerratt, J Robertson, Org. Lett. 2011, 13, 5964
Synthesis of NP25302
W P Unsworth, K Stevens, S G Lamont, J Robertson, Chem. Commun. 2011, 47, 7659
Stereospecificity in the Au-Catalysed Cyclisation of Monoallylic Diols. Synthesis of (+)-Iso-altholactone
K Stevens, J Robertson, Abstr. Pap. Am. Chem. Soc. 2011, 241, 255-ORGN
Total Synthesis of the Pyrrolizidine Alkaloid Natural Product NP25302 [abstract]
J Robertson, C North, J E R Sadig, Tetrahedron 2011, 67, 5011
Asymmetric Synthesis of the C(6–18) Bis(tetrahydropyran)spiroacetal Fragment of the Lituarines
J Robertson, K Clarke, R L Veech, WO 2010/120300
Process for the Preparation of (3R)-Hydroxybutyl (3R)-hydroxybutyrate by Enzymatic Enantioselective Reduction Employing Lactobacillus brevis Alcohol Dehydrogenase
J W Levell, J P Gunning, P L Burn, J Robertson, I D W Samuel, Org. Electron. 2010, 11, 1561
A Phosphorescent Poly(dendrimer) with Increased Viscosity for Solution-Processed OLED Devices
B Wu, A Mallinger, J Robertson, Org. Lett. 2010, 12, 2818
Synthesis of Taurospongin A
S Macnaughton, J Robertson, J Dallimore, Abstr. Pap. Am. Chem. Soc. 2010, 239, 1066-ORGN
Development of an Extended Aza-Achmatowicz Cyclisation: Progress Towards the Total Synthesis of Pandamarilactone-1 [abstract]
G C Feast, J Robertson, L W Page, Abstr. Pap. Am. Chem. Soc. 2010, 239, 389-ORGN
Aziridination of Tethered Allenes [abstract]
J Robertson, G C Feast, L V White, V A Steadman, T D W Claridge, Org. Biomol. Chem. 2010, 8, 3060
Structure and Reactivity of Bicyclic Methylene Aziridines Prepared by Intramolecular Aziridination of Allenes