SIMON E. LEWIS PUBLICATIONS
60.) “Structural investigation of sulfobetaines
and phospholipid monolayers at the air–water interface”, Elstone, N.*; Arnold,
T.; Skoda, M. W. A.; Lewis, S. E.; Li, P.; Hazell, G.; Edler, K. J.*, Phys.
Chem. Chem. Phys., 2022, 24, 22679, doi:10.1039/d2cp02695c
59.) “Azulene-based fluorescent chemosensor for
adenosine diphosphate”, López-Alled, C. M.; Park,
S. J.; Lee, D. J.; Murfin, L. C.; Kociok-Köhn, G.; Hann, J. L.; Wenk, J.*; James,
T. D.*; Kim, H. M.*; Lewis, S. E.*, Chem. Commun.,
2021, 57, 10608, doi:10.1039/d1cc04122c
58.) “Palladium-catalyzed
stereoselective domino arylation–acylation: an entry to chiral tetrahydrofluorenone scaffolds”, Dunås, P.; Paterson, A.
J.; Kociok-Köhn, G.; Rahm, M.; Lewis, S. E.*; Kann, N.*, Chem. Commun., 2021, 57, 6518, doi:10.1039/d1cc02160e
57.) “Azulene – A bright core for sensing and imaging”,
Murfin, L. C.*; Lewis, S. E., Molecules, 2021, 26, 353, doi:10.3390/molecules26020353
56.) “C4-aldehyde of guaiazulene: synthesis and
derivatisation”, Williams, G. E.; Kociok-Köhn, G.; James, T. D.; Lewis, S.
E.*, Org. Biomol. Chem., 2021, 19,
2502, doi:10.1039/d0ob02567d
55.) “Fluorescent small organic probes for biosensing”,
Tian, X.; Murfin, L. C.; Wu, L.*; Lewis, S. E.*; James, T. D.*, Chem. Sci.,
2021, 12, 3406, doi:10.1039/D0SC06928K
54.) “Colorimetric detection of Hg2+ with an
azulene-containing chemodosimeter via dithioacetal hydrolysis”, López-Alled, C. M.; Murfin, L. C.; Kociok-Köhn, G.; James, T.
D.*; Wenk, J.*; Lewis, S. E.*, Analyst, 2020, 145, 6262, doi:10.1039/d0an01404d
53.) “Azulenesulfonium and azulenebis(sulfonium)
salts: Formation by interrupted Pummerer reaction and subsequent derivatisation
by nucleophiles”, López-Alled, C. M.; Martin, F.
J. O.; Chen, K.-Y.; Kociok-Köhn, G.; James, T. D.; Wenk, J.; Lewis, S. E.*, Tetrahedron,
2020, 76, 131700, doi:10.1016/j.tet.2020.131700
52.) “Azulene functionalization by iron-mediated
addition to a cyclohexadiene scaffold”, Dunås, P.; Murfin, L. C.; Nilsson, O.
J.; Jame, N.; Lewis, S. E.*; Kann, N.*, J. Org.
Chem., 2020, 85, 13453, doi:10.1021/acs.joc.0c01412
51.) “Palladium catalyzed
stereoselective arylation of biocatalytically derived
cyclic 1,3-dienes: Chirality transfer via a Heck-type mechanism”, Paterson,
A. J.; Dunås, P.; Rahm, M.; Norrby, P.-O.; Kociok-Köhn,
G.; Lewis, S. E.*; Kann, N.*, Org. Lett., 2020, 22, 2464, doi:10.1021/acs.orglett.0c00708
50.) “(Fluoro)quinolones and quinolone resistance genes
in the aquatic environment: A river catchment perspective”, Castrignanò, E.; Kannan, A. M.; Proctor, K.; Petrie, B.; Hodgen, S.; Feil, E. J.; Lewis, S. E.; Lopardo, L.; Camacho-Muñoz,
D.; Rice, J.; Cartwright, N.; Barden, R.; Kasprzyk-Hordern, B.*, Water
Research, 2020, 182, 116015, doi:10.1016/j.watres.2020.116015
49.) “A Colorimetric
chemosensor based on a Nozoe azulene that detects fluoride in aqueous/alcoholic
media”, Murfin, L. C.; Chiang, K. X. C.; Lyall, C. L.; Williams, G. T.;
Wenk, H.*; Jenkins, T.*; James, T. D.*; Lewis, S. E.*, Frontiers in Chemistry, 2020,
doi: 10.3389/fchem.2020.00010
48.) “A simple,
azulene-based colorimetric probe for the detection of nitrite in water”, Murfin,
L. C.; López-Alled, C. M.; Sedgwick, A. C.; Wenk, J.*;
James, T. D.*; Lewis, S. E.*, Frontiers
of Chemical Science and Engineering, 2020,
doi:10.1007/s11705-019-1790-7
47.) “Sidechain
Diversification of Grandifloracin Allows Identification of Analogues with
Enhanced Anti‐Austerity Activity against Human PANC‐1 Pancreatic Cancer Cells”, Alexander, B. E.; Sun,
S.; Palframan, M. J.; Kociok‐Köhn, G.; Dibwe, D. F.; Watanabe,
S.; Caggiano, L.*; Awale, S.*; Lewis, S. E.*, ChemMedChem,
2020, 15, 125, doi:10.1002/cmdc.201900549
46.) “Azulene-Derived
Fluorescent Probe for Bioimaging: Detection of Reactive Oxygen and Nitrogen
Species by Two-Photon Microscopy”, Murfin, L. C.; Weber, M.; Park, S. J.; Kim, W.
T.; Lopez-Alled, C. M.; McMullin, C. L.;
Pradaux-Caggiano, F.; Lyall, C. L.; Kociok-Köhn,
G.; Wenk, J. H.; Bull, S. D.; Yoon, J.; Kim, H. M.*; James, T. D.*; Lewis, S.
E.*, J. Am. Chem. Soc. 2019, 141, 19389-19396. doi: 10.1021/jacs.9b09813
45.) “Selective
Iron-Mediated C- and O-Addition of Phenolic Nucleophiles to a Cyclohexadiene
Scaffold Using Renewable Precursors”, Dunås,
P.; Paterson, A. J.; Kociok-Köhn,
G.; Lewis, S. E.*; Kann, N.*, 2019, 7, 7155-7162. doi:10.1021/acssuschemeng.9b00127
44.) “Partial Cation
Substitution Reduces Iodide Ion Transport in Lead Iodide Perovskite Solar Cells”,
Ferdani, D.; Pering, S.; Ghosh, D.; Kubiak, P.; Walker, A.; Lewis, S.
E.; Johnson, A. L.; Baker, P. J.; Islam, M. S.; Cameron, P. J., Energy & Environmental Science, 2019, 12, 2264-2272. doi: 10.1039/c9ee00476a
43.) “Azulenes with
aryl substituents bearing pentafluorosulfanyl groups: synthesis, spectroscopic
and halochromic properties”, Webster, S. J.; López-Alled,
C. M.; Liang, X.; McMullin, C. L.; Kociok-Köhn, G.; Lyall, C. L.; James, T. D.;
Wenk, J.; Cameron, P. J.; Lewis, S. E.*, New
Journal of Chemistry, 2019, 43, 992-1000. doi:10.1039/C8NJ05520C
42.) “Azulene–Thiophene–Cyanoacrylic
acid dyes with donor-π-acceptor structures. Synthesis, characterisation
and evaluation in dye-sensitized solar cells”, Cowper, P*; Pockett, A.; Kociok-Köhn, G.; Cameron, P. J.; Lewis, S. E*,
Tetrahedron, 2018, 74, 2775–2786. doi:10.1016/j.tet.2018.04.043
41.) “Self-assembly
and surface behaviour of pure and mixed zwitterionic amphiphiles in a deep
eutectic solvent”, Sanchez-Fernandez, A.; Moody, G. L.; Murfin, L. C.; Arnold,T.; Jackson, A. J.; King, S. M.; Lewis, S. E.; Edler,
K. J., Soft Matter, 2018, 14, 5525-5536. doi:10.1039/c8sm00755a
40.) “Enantioselective
transformation of fluoxetine in water and its ecotoxicological relevance”, Andrés-Costa,
M. J.; Proctor, K.; Sabatini, M. T.; Gee, A. P.; Lewis, S. E.; Pico, Y.;
Kasprzyk-Hordern, B., Sci. Rep., 2017, 7, 15777. doi:10.1038/s41598-017-15585-1
39.) “Azetidinium lead
iodide for perovskite solar cells”, Pering, S. R.; Deng, W.; Troughton, J.
R.; Kubiak, P. S.; Ghosh, D.; Niemann, R. G.; Brivio, F.; Jeffrey, F. E.; Walker,
A. B.; Islam, M. S.; Watson, T. M.; Raithby, P. R.; Johnson, A. L.; Lewis, S.
E.; Cameron; P. J.*, J. Mater. Chem. A,
2017,5, 20658-20665. doi:10.1039/C7TA07545F
38.) “Biocatalytic
dearomatisation of para-fluorobenzoic acid – Access to versatile homochiral
building blocks with quaternary centres”, Nash, T. J.; Wharry, S.; Moody,
T. S.*; Lewis, S. E.*, Chimica Oggi, 2017, 35, 90–94. http://www.teknoscienze.com/tks_article/biocatalytic-dearomatisation-of-para-fluorobenzoic-acid-access-to-versatile-homochiral-building-blocks-with-quaternary-centres/
37.) “Azulene–boronate
esters: colorimetric indicators for fluoride in drinking water”, López-Alled,
C. M.; Sanchez-Fernandez, A.; Edler, K. J.; Sedgwick, A. C.; Bull, S. D.; McMullin,
C. L.; Kociok-Köhn, G.; James, T. D.*; Wenk, J.*; Lewis, S. E.*, Chem. Commun.,
2017, 53, 12580–12583. doi:10.1039/c7cc07416f
36.) “Phosphorus-substituted
azulenes accessed via direct Hafner reaction of a phosphino
cyclopentadienide”, Gee, A. P.; Cosham, S. D.; Johnson, A. L.; Lewis, S.
E.* Synlett,
2017, 973–975. doi:10.1055/s-0036-1589936
35.) “What difference does a thiophene make? Evaluation
of a 4,4’-bis(thiophene) functionalised 2,2’-bipyridyl copper(I) complex in a
dye-sensitized solar cell”, Wills, K. A.; Mandujano-Ramírez,
H. A.; Merino, G.; Oskam, G.; Cowper, P.; Jones, M. D.*; Cameron, P. J.*;
Lewis, S. E.* Dyes and Pigments, 2016,
134, 419-426. doi:10.1016/j.dyepig.2016.07.023
34.) “Asymmetric Dearomatization
Under Enzymatic Conditions”, Lewis, S. E. in Asymmetric Dearomatization Reactions (You, S.-L. ed.) Wiley-VCH, 2016, pp 279–346. doi:10.1002/9783527698479.ch12
33.) “Langmuir monolayers composed of single and double
tail sulfobetaine lipids”, Hazell, G.; Gee, A.
P.; Arnold, T.; Edler, K.*; Lewis, S. E.
J. Colloid Interface Sci., 2016, 474, 190-198. doi:10.1016/j.jcis.2016.04.020
32.) “Azulenesulfonium Salts: Accessible, Stable and Versatile Reagents for
Cross-Coupling”, Cowper, P.*; Jin, Y.; Turton, M.
D.; Kociok-Köhn, G.; Lewis, S. E.* Angew. Chem. Int. Edn., 2016, 55, 2564–2568. doi:10.1002/anie.201510666
31.) “Biotransformations
of Arenes: An Overview”, Lewis, S. E. in Arene Chemistry: Reaction
Mechanisms and Methods for Aromatic Compounds (Mortier, J. ed.) Wiley-VCH, 2015,
pp 915–937. doi:10.1002/9781118754887.ch32
30.) “Tricarbonyliron(0) complexes of
bio-derived η4 cyclohexadiene ligands: An approach to analogues
of oseltamivir”, ten
Broeke, M.; Ali Khan, M.; Kociok-Köhn, G.; Kann, N.; Lewis, S. E.* J. Organomet. Chem., 2015,
799-800, 19–29. doi:10.1016/j.jorganchem.2015.09.005
29.) “Cycloparaphenylenes and related nanohoops”,
Lewis, S. E.* Chem. Soc. Rev., 2015, 44, 2221–2304. doi:10.1039/c4cs00366g
28.) “Direct core functionalisation
of naphthalenediimides by iridium catalysed C–H borylation”, Lyall, C. L.; Shotton,
C. C.; Pérez-Salvia, M.; Pantoş, G. D.*; Lewis, S. E.* Chem. Commun.,
2014, 50, 13837–13840, doi:10.1039/c4cc06522k
27.) “C–H functionalization of sp3 centers
with aluminum: a computational and mechanistic study
of the Baddeley reaction of decalin”, Lyall,C.
L.; Sato, M.; Uosis-Martin, M.; Asghar, S. F.; Jones, M. D.; Williams, I. H.*;
Lewis, S. E.* J. Am. Chem. Soc., 2014, 136, 13745–13753, doi:10.1021/ja5062246
26.) “A new assay for rhamnolipid detection—important virulence
factors of Pseudomonas aeruginosa”, Laabei, M.;
Jamieson, W. D.; Lewis, S. E.; Diggle, S. P.; Jenkins, A. T. A.* Appl. Microbiol.
Biotech., 2014, 98, 7199–7209, doi:10.1007/s00253-014-5904-3
25.) “The Enone Motif of (+)-Grandifloracin is
Not Essential for “Anti-Austerity” Antiproliferative Activity”, Ali Khan, M.; Wood, Pauline J.;
Lamb-Guhren, N. M.; Caggiano, L.; Kociok-Köhn, G.; Tosh, D.; Lewis, S. E.* Bioorg. Med. Chem. Lett., 2014, 24, 2815–2819 doi: 10.1016/j.bmcl.2014.04.111
24.) “Applications of biocatalytic
arene ipso,ortho cis-dihydroxylation
in synthesis”, Lewis, S. E.* Chem. Commun.,
2014, 50, 2821–2830 doi:10.1039/c3cc49694e
23.) “Benzoate dioxygenase from Ralstonia eutropha B9 – unusual
regiochemistry of dihydroxylation permits rapid
access to novel chirons”, Griffen,
J. A.; Kenwright, S. J.; Abou-Shehada,
S.; Wharry, S.; Moody, T. S.*; Lewis, S. E.*
Org. Chem. Front., 2014, 1, 79–90 doi:10.1039/c3qo00057e
22.) “Investigation of a copper(I) biquinoline
complex for application in dye-sensitized solar cells”, Wills, K. A.; Mandujano-Ramírez, H. J.; Merino, G.; Mattia, D.; Hewat, T.; Robertson, N.; Oskam,
G.; Jones, M. D.; Lewis, S. E.; Cameron, P. J. RSC Advances, 2013,
3, 23361–23369 doi:10.1039/c3ra44936j
21.) “A Model System for the Synthesis of
Complanadine Alkaloids by ‘Diverted Kondrat’eva’
Oxazole–Olefin Cycloaddition”, Uosis-Martin, M.; Pantos, G.
D.; Mahon, M. F.; Lewis, S. E.* J. Org. Chem., 2013, 78,
6253–6263 doi:10.1021/jo401014n
20.) “New
Aminocyclitols with Quaternary Stereocentres via Acylnitroso Cycloaddition with
an ipso,ortho-Arene Dihydrodiol”,
Griffen, J. A.; White, J. C.; Kociok-Köhn, G.; Lloyd,
M. D.; Wells, A.; Arnot, T. C.; Lewis, S. E.* Tetrahedron, 2013, 69,
5989–5997. doi:10.1016/j.tet.2013.04.033
19.) “Aliphatic C–H Activation with Aluminium Trichloride–Acetyl
Chloride: Expanding the Scope of the Baddeley Reaction for the Functionalisation
of Saturated Hydrocarbons”, Lyall, C. L.; Uosis-Martin, M.; Lowe, J. P.;
Mahon, M. F.; Pantoş, G. D.; Lewis, S. E.* Org. Biomol.
Chem., 2013, 11,
1468–1475, doi:10.1039/c2ob26765a
18.) "Valuable
New Cyclohexadiene Building Blocks via Cationic η5 Iron Carbonyl Complexes Derived from a
Microbial Arene Oxidation Product”,
Ali Khan, M.; Mahon, M. F.; Lowe, J. P.; Stewart, A. J. W.; Lewis, S. E.* Chem.
Eur. J., 2012, 18,
13480–13493, doi:10.1002/chem.201202411p
17.) "Photooxygenation of a
Microbial Arene Oxidation Product and Regioselective Kornblum–DeLaMare Rearrangement. Total Synthesis of Zeylenols and Zeylenones”, Palframan, M. J.; Kociok-Köhn, G.; Lewis, S. E.* Chem. Eur. J., 2012, 18, 4766–4774, doi:10.1002/chem.201104035
16.) “TRPA1 Mediates Spinal Antinociception Induced by Acetaminophen
and the Cannabinoid Δ9-Tetrahydrocannabiorcol”, Andersson, D. A.;
Gentry, C.; Alenmyr, L.; Killander,
D.; Lewis, S. E.; Andersson, A.; Bucher, B.; Galzi,
J.-L.; Sterner, O.; Bevan, S.; Högestätt, E. D.;
Zygmunt, P. M. Nature Commun., 2011, 2,
551, doi:10.1038/ncomms1559
15.) “A Cobalt Complex of a Microbial Arene Oxidation
Product”, van der Waals, D.; Pugh, T.; Ali Khan, M.; Stewart, A. J. W.;
Johnson, A. L.; Lewis, S. E.* Chem.
Central J., 2011, 5, 80, doi:10.1186/1752-153X-5-80
14.) “Concise Synthesis of 1,4a-Bifunctionalised
Decalin Building Blocks by C–H Activation of Decalin”, Uosis-Martin,
M.; Mahon, M. F.; Yevglevskis, M.; Lewis, S. E.* Synlett, 2011, 2211–2213, doi: 10.1055/s-0030-1261184
13.) “Synthetic methods Part (II):
oxidation and reduction methods”, Asghar, S. F.; Lewis, S. E.* Annu. Rep. Prog. Chem., Sect. B: Org. Chem.,
2011, 107, 34–67, doi:10.1039/c1oc90012a
12.) “Total Synthesis of
(+)-Grandifloracin by Iron Complexation of a Microbial Arene Oxidation Product”,
Palframan, M. J.; Kociok-Köhn, G.; Lewis, S. E.* Org. Lett., 2011, 13, 3150–3153, doi:10.1021/ol201057r
11.) “Expanding the chiral pool: oxidation of meta-bromobenzoic
acid by R. eutrophus B9 allows access to new reaction manifolds”,
Griffen, J. A.; Le Coz, A. M.; Kociok-Köhn, G.; Ali Khan, M.; Stewart, A. J. W;
Lewis, S. E.* Org. Biomol. Chem., 2011,
9, 3920–3928, doi:10.1039/c1ob05131h
10.) “Inosaminoacids: novel inositol–amino acid hybrid structures accessed by microbial arene oxidation”, Pilgrim, S.; Kociok-Köhn, G.; Lloyd, M. D.; Lewis, S. E.* Chem. Commun., 2011, 47, 4799–4801 doi:10/1039/c1cc10643k
9.) “Accessing the antipodal series in microbial arene
oxidation: a novel diene rearrangement induced by tricarbonyliron(0)
complexation“, Ali Khan, M.; Lowe, J. P.; Johnson, A. L.; Stewart, A. J.
W.; Lewis, S. E.* Chem. Commun., 2011, 47,
215–217 doi:10.1039/c0cc01169j
8.) “Iron(0)tricarbonyl Complexes of Microbially-Derived
Cyclohexadiene Ligands Containing Quaternary Stereocenters”,
Ali Khan, M.; Mahon, M. F.; Stewart, A. J. W.; Lewis, S. E.* Organometallics, 2010, 29, 199–204. doi:10.1021/om9009069
7.) “Transannular decarboxylative Claisen rearrangement
reactions for the synthesis of sulfur-substituted vinylcyclopropanes”,
Craig, D.*; Gore, S. J.; Lansdell, M. I.; Lewis, S.
E.; Mayweg, A. V. M.; White, A. J. P. Chem. Commun., 2010, 46, 4991–4993.
6.) “Synthesis and Characterisation of Novel Alkane-α,ω-diyl bis(silyl
triflates)”, Baker, T.; Lewis, S. E.* Synth. Commun., 2010, 40,
2747–2752. doi:10.1080/00397910903318724
5.) “Crystallographic rationalization of the reactivity and
spectroscopic properties of (2R)-S-(2,5-dihydroxyphenyl)cysteine”,
Kociok-Köhn, G.; Lewis, S. E.* Acta Cryst., 2010, C66,
o187–o189. doi:10.1107/S0108270110005780
4.) “Synthetic methods: Part (ii) Oxidation and reduction
methods”, Lewis, S. E.* Annu.
Rep. Prog. Chem., Sect. B: Org. Chem., 2010, 106, 34–75. doi:10.1039/b927087f
3.) “Synthetic methods: Part (ii) Oxidation and reduction methods”,
Lewis, S. E.* Annu. Rep. Prog.
Chem., Sect. B: Org. Chem., 2009, 105, 35–74. doi:10.1039/b822050f
2.) “Decarboxylative
Claisen rearrangements of diallyl 2-sulfonylmalonates: remarkable regioselectivity
in the reaction of bifunctional substrates”, Craig, D.*; Lansdell,
M.; Lewis, S. E. Tetrahedron Lett.,
2007, 48, 7861–7864.
doi:10.1016/j.tetlet.2007.08.130
1.) “Recent advances in the chemistry of macroline,
sarpagine and ajmaline-related indole alkaloids”, Lewis, S. E.* Tetrahedron, 2006, 62, 8655–8681. doi:10.1016/j.tet.2006.06.017