S. Swanson

发表

A practical drug discovery project at the undergraduate level.

J. Liddle, M. Fray, D. Coe, 2013, Drug discovery today.

Trichodiene biosynthesis and the stereochemistry of the enzymatic cyclization of farnesyl pyrophosphate

D. Cane, C. Pargellis, H. Ha, 1985 .

Quantification of Intracellular Accumulation and Retention of Lysosomotropic Macrocyclic Compounds by High-Throughput Imaging of Lysosomal Changes.

U. Norinder, S. Swanson, Vesna Munic Kos, 2019, Journal of pharmaceutical sciences.

Cyclisation of farnesyl pyrophosphate to γ-bisabolene in tissue cultures of Andrographis paniculata

C. Gilmore, H. Mackie, S. Swanson, 1982 .

α-Fluoromethyl-n-methyl-phenylsulphoximine: a new fluoromethylenation reagent

H. Finch, S. Swanson, M. Boys, 1988 .

Synthesis of Functionalized Pyridines via a Regioselective Oxazoline Promoted C-H Amidation Reaction.

J. P. Harrity, P. Procopiou, S. Swanson, 2016, Organic letters.

A mild and regioselective route to functionalized quinazolines.

J. P. Harrity, P. Procopiou, S. Swanson, 2015, Chemistry.

Switching regiocontrol in 1-aryl-substituted cyclohexadienyliron complexes in a formal total synthesis of lycoramine

G. Stephenson, S. Swanson, Elizabeth J. Sandoe, 1996 .

Studies on the stereochemical assignment of 3-acylidene 2-oxindoles.

H. Adams, A. Meijer, J. P. Harrity, 2014, Organic & biomolecular chemistry.

A convergent strategy towards febrifugine and related compounds.

J. P. Harrity, P. Procopiou, S. Swanson, 2018, Organic & biomolecular chemistry.

Oxazoline-Promoted Rh-Catalyzed C-H Amidation of Benzene Derivatives with Sulfonamides and Trifluoroacetamide. A Comparative Study.

J. P. Harrity, P. Procopiou, S. Swanson, 2016, The Journal of organic chemistry.

Transition metal mediated asymmetric synthesis, part 151 directing group competition in organoiron intermediates in the synthesis of (±)-O-methyljoubertiamine

H. Finch, D. Owen, G. Stephenson, 1993 .

Organometallic equivalents of cyclohexenone di-cation synthons for the total synthesis of O-methyljoubertiamine☆

H. Finch, D. Owen, G. Stephenson, 1991 .

Biosynthesis of γ-bisabolene in tissue cultures of Andrographispaniculata

C. Gilmore, H. Mackie, S. Swanson, 1984 .

Investigation of a Late‐Stage Derivatization Approach to Isatogens: Discovery of New Reaction Pathways

J. P. Harrity, P. Procopiou, S. Swanson, 2016 .

2-Iodoisatogens: versatile intermediates for the synthesis of nitrogen heterocycles.

J. P. Harrity, P. Procopiou, S. Swanson, 2015, Organic letters.

Aryl-substituted cyclohexadienyl complexes: Novel intermediates for an organometallic approach to and alkaloid synthesis.

H. Finch, D. Owen, G. Stephenson, 1990 .

Phenyl directing groups in the demethoxylation route to tricarbonyl(η5-cyclohexadienyl)iron(1 +) complexes

H. Finch, D. Owen, G. Stephenson, 1990 .

Transition metal mediated organic synthesis, part 11: 2-aryl substituents: new directing groups in cyclohexadienyl π-complexes

H. Finch, D. Owen, G. Stephenson, 1989 .

Transition Metal‐Mediated Organic Synthesis. Part 11. 2‐Aryl‐Substituents: New Directing Groups in Cyclohexadienyl π‐Complexes.

H. Finch, D. Owen, G. Stephenson, 1989 .

Ethyl-substituted erythromycin derivatives produced by directed metabolic engineering.

K A Reynolds, K. Reynolds, L. Katz, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Condensed heteroaryl derivatives for use as p38 kinase inhibitors in the treatment of, inter alia, rheumatoid arthritis.

P. Bamborough, R. Angell, Timothy Longstaff, 2003 .

Synthesis and inclusion properties of twelve-membered carbocyclic hosts

S. Swanson, D. Macnicol, 1977 .