Items where Author is "Snape, Timothy J."

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Dennison, Sarah Rachel orcid iconORCID: 0000-0003-4863-9607, Malik, Erum, Phoenix, David A., Snape, Timothy J., Harris, Frederick, Singh, Jaipaul orcid iconORCID: 0000-0002-3200-3949 and Morton, Leslie Hugh Glyn (2021) Linearized esculentin-2EM shows pH dependent antibacterial activity with an alkaline optimum. Molecular and Cellular Biochemistry, 476 . pp. 3729-3744. ISSN 0300-8177

Fahs, Sara, Patil-Sen, Yogita orcid iconORCID: 0000-0002-4286-8874 and Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2015) Foldamers as Anticancer Therapeutics: Targeting Protein-Protein Interactions and the Cell Membrane. ChemBioChem, 16 (13). pp. 1840-1853. ISSN 14394227

Sherer, Chris and Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2015) Heterocyclic scaffolds as promising anticancer agents against tumours of the central nervous system: Exploring the scope of indole and carbazole derivatives. European Journal of Medicinal Chemistry, 97 . pp. 552-560. ISSN 02235234

Ameen, Dana and Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2015) A Baker–Venkataraman retro-Claisen cascade delivers a novel alkyl migration process for the synthesis of amides. Tetrahedron Letters, 56 (14). pp. 1816-1819. ISSN 00404039

Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 and Warr, Tracy (2014) Approaches Toward Improving the Prognosis of Pediatric Patients With Glioma: Pursuing Mutant Drug Targets With Emerging Small Molecules. Seminars in Pediatric Neurology, 22 (1). pp. 28-34.

Lal, Samridhi and Snape, Timothy J. (2014) Towards a sustainable synthesis of aniline-derived amides using an indirect chemoenzymatic process: challenges and successes. RSC Adv., 4 (4). pp. 1609-1615. ISSN 2046-2069

Prabhu, Saurabh, Dennison, Sarah R., Lea, Bob, Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491, Nicholl, Iain D., Radecka, Iza and Harris, Frederick (2013) Anionic Antimicrobial and Anticancer Peptides from Plants. Critical Reviews in Plant Sciences, 32 (5). pp. 303-320. ISSN 0735-2689

Ameen, Dana and Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2013) Chiral 1,1-diaryl compounds as important pharmacophores. MedChemComm, 4 (6). p. 893. ISSN 2040-2503

Dennison, Sarah R., Phoenix, David A. and Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2013) Synthetic oligoureas of metaphenylenediamine mimic host defence peptides in their antimicrobial behaviour. Bioorganic & Medicinal Chemistry Letters, 23 (9). pp. 2518-2521. ISSN 0960894X

Lal, Samridhi and Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2012) Exploitation of a Candida antarctica lipase B-catalysed in situ carboxylic acid activation method for the synthesis of acetanilides. Journal of Molecular Catalysis B: Enzymatic, 83 . pp. 80-86. ISSN 13811177

Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491, Karakoula, Katherine, Rowther, Farzana and Warr, Tracy (2012) 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. RSC Advances, 2 (19). p. 7557. ISSN 2046-2069

Dennison, Sarah R., Akbar, Zaheer, Phoenix, David A. and Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2012) Interactions between suitably functionalised conformationally distinct benzanilides and phospholipid monolayers. Soft Matter, 8 (11). p. 3258. ISSN 1744-683X

Dennison, Sarah R., Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 and Phoenix, David A. (2012) Thermodynamic interactions of a cis and trans benzanilide with Escherichia coli bacterial membranes. European Biophysics Journal, 41 (8). pp. 687-693. ISSN 0175-7571

March-Cortijos, Andrea and Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2009) Towards a chemo-enzymatic method for the asymmetric synthesis of β-amino tertiary alcohols. Organic & Biomolecular Chemistry, 7 (24). pp. 5163-5165. ISSN 1477-0520

March-Cortijos, Andrea and Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2009) Towards a chemo-enzymatic method for the asymmetric synthesis of β-amino tertiary alcohols. Organic & Biomolecular Chemistry, 7 (24). p. 5163. ISSN 1477-0520

Clayden, Jonathan, Lemiègre, Loïc, Morris, Gareth A., Pickworth, Mark, Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 and Jones, Lyn (2008) Helix Persistence and Breakdown in Oligoureas of Metaphenylenediamine: Apparent Diastereotopicity as a Spectroscopic Marker of Helix Length in Solution. Journal of the American Chemical Society, 130 (45). pp. 15193-15202. ISSN 0002-7863

Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2008) A truce on the Smiles rearrangement: revisiting an old reaction—the Truce–Smiles rearrangement. Chemical Society Reviews, 37 (11). pp. 2452-2458. ISSN 0306-0012

Cortijos, Andrea March and Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2008) Enzymatic desymmetrisation of (2-hydroxymethyl-oxiranyl)-methanol in organic solvents. Tetrahedron: Asymmetry, 19 (15). pp. 1761-1763. ISSN 09574166

Betson, Mark S., Bracegirdle, Ann, Clayden, Jonathan, Helliwell, Madeleine, Lund, Andrew, Pickworth, Mark, Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 and Worrall, Christopher P. (2007) 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. Chemical Communications (7). p. 754. ISSN 1359-7345

Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2007) Recent advances in the semi-pinacol rearrangement of α-hydroxy epoxides and related compounds. Chemical Society Reviews, 36 (11). p. 1823. ISSN 0306-0012

Bailey, Kevin R., Ellis, Andrew J., Reiss, Renate, Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 and Turner, Nicholas J. (2007) A template-based mnemonic for monoamine oxidase (MAO-N) catalyzed reactions and its application to the chemo-enzymatic deracemisation of the alkaloid (±)-crispine A. Chemical Communications (35). p. 3640. ISSN 1359-7345

Snape, Timothy J. orcid iconORCID: 0000-0003-2766-4491 (2006) Application of the semi-pinacol rearrangement towards the generation of alkenyl-substituted quaternary carbon centres. Organic & Biomolecular Chemistry, 4 (22). p. 4144. ISSN 1477-0520

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