Timsnape.co.uk

Exploitation of a Candida antarctica lipase B-catalyzed in situ carboxylic acid activation method for the
synthesis of acetanilides: Samridhi Lal and Timothy J. Snape,* Journal of Molecular Catalysis B: Enzymatic,
2012, In Press.
Thermodynamic interactions of a cis and trans benzanilide with Escherichia coli bacterial membranes: Sarah R.
Dennison, David A. Phoenix and Timothy J. Snape, European Biophysics Journal, 2012, doi:10.1007/s00249-
012-0835-3.
Exploiting conformationally restricted N,N’-dimethyl-N,N’-diarylureas as biologically active C=C double bond
analogues: synthesis and biological evaluation of combretastatin A-4 analogues: Timothy J. Snape,* Katherine
Karakoula, Farzana Rowther and Tracy Warr, RSC Adv., 2012, 2 (19), 7557 - 7560.
Synthesis of 1,3-disubstituted azetidines via a tandem ring-opening ring-closing procedure: Andrea March-
Cortijos, Timothy Snape* and Nicholas Turner, Synlett, 2012, 23, 1511-1515.
Interactions between suitably functionalised conformationally distinct benzanilides and phospholipid
monolayers: Sarah R. Dennison, Zaheer Akbar, David A. Phoenix and Timothy J. Snape,*Soft Matter, 2012, 8
(11), 3258 - 3264.
Exploiting conformationally restricted ureas as biologically active C=C double bond analogues against GBM
cells in vitro, TJ Snape, A Karakoula, F Rowther and TJ Warr, Neuro. Oncol., 2011, 13 (suppl 2): ii1-ii14.
Towards establishing the effects and mechanism of action of a series of indoles in an in vitro chemosensitivity
system for glioma treatment, Saurabh Prabhu, Frederick Harris, Robert Lea and Timothy J Snape, Neuro.
Oncol.,
2011, 13 (suppl 2): ii1-ii14.
Effects of Momordica charantia fruit extract with the combination of temozolamide and cisplatin in the
treatment of glioma cancer: G. Manoharan, R. W. Lea, T. J. Snape, J. Singh*, Proc. Physiol. Soc., 2010, 18,
PC22.
Roberts, Stanley Michael; Santoro, Maria Gabriella; Jadhav, Vasudev; Happe, Alan Michael; Evans, Paul;
Ross, Nicolette Christa; Snape, Timothy James, Patent Number: US 07759399, Publication Date: July 20,
2010, Crawford Healthcare Holdings Limited .
Understanding the chemical basis of drug stability and degradation: Timothy J. Snape*, Alison M. Astles and
Janice Davies, The Pharmaceutical Journal, 2010, 285, 416.
The process of drug development from the laboratory bench to the market: Timothy J. Snape* and Alison M.
Astles, The Pharmaceutical Journal, 2010, 285, 272.
The rational redesign of penicillins to help combat penicillin resistance: Timothy J. Snape* and Alison M.
Astles, The Pharmaceutical Journal, 2010, 285,162.
Take a close look at citalopram and you can predict its contraindications: Timothy J. Snape* and Alison M.
Astles, The Pharmaceutical Journal, 2010, 285, 59 - Cover Article.
Monoamine Oxidase (MAO-N) Catalysed Reactions: Application Towards the Chemo-Enzymatic
Deracemisation of the Alkaloid (±)-Crispine A: Andrew J. Ellis, Renate Reiss, Timothy J. Snape and Nicholas
J. Turner, Practical Methods for Biocatalysis and Biotransformations, 2009, John Whittall, Peter Sutton (Eds),
Wiley, Chapter 11.1.
Towards a chemo-enzymatic method for the asymmetric synthesis of β-amino tertiary alcohols: Andrea March-
Cortijos and Timothy J. Snape*, Org. Biomol. Chem., 2009, 7, 5163-5165.
Versatility of a new bioinorganic catalyst: Palladized cells of Desulfovibrio desulfuricans and application to
dehalogenation of flame retardant materials, K. Deplanche; T. J. Snape; S. Hazrati; S. Harrad; L. E. Macaskie*,
Environmental Technology, 2009, 30, 7, 681–692.
Helix Persistence and Breakdown in Oligoureas of Metaphenylenediamine: Apparent Diastereotopicity as a
Spectroscopic Marker of Helix Length in Solution: Jonathan Clayden*, Loic Lemiegre, Gareth A. Morris,
Mark Pickworth, Timothy J. Snape and Lyn H. Jones, J. Am. Chem. Soc., 2008, 130, 15193–15202.
α-Arylation of Aryl-Ketones: Expanding the Scope of the Truce-Smiles Rearrangement: Timothy J. Snape*,
Synlett, 2008, 2689-2691.
A Truce on the Smiles Rearrangement: Revisiting an Old Reaction – The Truce-Smiles Rearrangement:
Timothy J. Snape*, Chem. Soc. Rev., 2008, 11, 2452-2458.
A biogenic catalyst for hydrogenation, reduction and selective dehalogenation in non-aqueous solvents: N. J.
Creamer, K. Deplanche, T. J. Snape, I. P. Mikheenko, P. Yong, D. Samyahumbi, J. Wood, K. Pollmann, S.
Selenska-Pobell and L. E. Macaskie*, Hydrometallurgy, 2008, 94, 138-143.
Enzymatic desymmetrisation of (2-hydroxymethyl-oxiranyl)-methanol in organic solvents: Andrea March
Cortijos and Timothy J. Snape*, Tetrahedron: Asymmetry, 2008, 19, 15, 1761-1763.
Recent Advances in the Semi-Pinacol Rearrangement of α-Hydroxy Epoxides and Related Compounds:
Timothy J. Snape*, Chem. Soc. Rev., 2007, 36, 11, 1823-1842.
A Template-Based Mnemonic for Monoamine Oxidase (MAO-N) Catalyzed Reactions and its Application
Towards the Chemo-Enzymatic Deracemisation of the Alkaloid (±)-Crispine A: Kevin R. Bailey, Andrew J.
Ellis, Renate Reiss, Timothy J. Snape* and Nicholas J. Turner*, Chem. Commun., 2007, 3640-3642.
Designated a Chem. Commun. “Hot Article”
Achieving conformational control over C-C, C-N and C-O bonds in biaryls, N,N’-diarylureas and diaryl ethers:
advantages of a relay axis: Mark S. Betson, Ann Bracegirdle, Jonathan Clayden*, Madeleine Helliwell,
Andrew Lund, Mark Pickworth, Timothy J. Snape and Christopher P. Worrall, Chem. Commun., 2007, 7, 754-
756.
Application of the Semi-Pinacol Rearrangement Towards the Generation of Alkenyl-Substituted Quaternary
Carbon Centres: Timothy J. Snape*, Org. Biomol. Chem., 2006, 4, 4144-4148.
Induction of Apoptosis in Estrogen-Receptor Negative Breast Cancer Cells by Natural and Synthetic
Cyclopentenones: Role of the IKK/NF-κB Pathway: Ciucci A, Gianferretti P, Piva R, Guyot T, Snape TJ,
Roberts SM and Santoro MG*, Mol. Pharmacol., 2006, 70, 1812-1821.
Synthesis of 4-azacyclopent-2-enones and 5,5-dialkyl-4-azacyclopent-2-enones: Dauvergne J, Happe AM*,
Jadhav V, Justice D, Matos MC, McCormack PJ, Pitts MR, Roberts SM, Singh SK, Snape TJ, Whittall J,
Tetrahedron, 2004, 60, 2559-2567.
Synthesis and revision of the stereochemistry of a cyclopentenone natural product isolated from ascomycete
strain A23-98:Bickley JF, Roberts SM, Santoro AG, Snape TJ*, Tetrahedron, 2004, 60, 2569-2576.
The IκB kinase IKK is the molecular target for anti-herpetic cyclopentenones: Amici C, Belardo G, Ciucci A,
Volpi C, Guyot T, Evans P, Happe A, Snape T, Roberts S, Santoro MG*, Antiviral Research, 2003, 57, 3,
A58-A58.
Roberts Stanley Michael; Ross Nicolette Christa; Jadhav Vasudev; Evans Paul; Snape Timothy James; Happe Alan Michael; Santoro Gabriella Maria, Patent Number: AU2003224244, Publication Date: 2003-10-13, Charterhouse Therapeutics Ltd.

Source: http://www.timsnape.co.uk/Publications%20list.pdf

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