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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.

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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

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