Andrew Marsh

Associate Professor
University of Warwick, Coventry, UK
go.warwick.ac.uk/marshgroup Associate Professor Department of Chemistry University of Warwick CV4 7AL

Publications

  • A G 4 ·K + Hydrogel Stabilized by an Anion DOI: 10.1021/ja507506c
  • Unexpected evolutionary proximity of eukaryotic and cyanobacterial enzymes responsible for biosynthesis of retinoic acid and its oxidation DOI: 10.1039/c3mb70447e
  • Use of freely available and open source tools for in silico screening in chemical biology DOI: 10.1021/ed400302u
  • A chemical genomics approach to identification of interactions between bioactive molecules and alternative reading frame proteins DOI: 10.1039/c3cc44647f
  • Nanostructures from self-assembling triazine tertiary amine n-oxide amphiphiles DOI: 10.1002/cphc.201300775
  • Oxidation of tertiary amine-derivatized surfaces to control protein adhesion DOI: 10.1021/la4003719
  • Challenges and solutions for personalizing medicines DOI: 10.1016/j.hlpt.2012.01.010
  • Nanodiamond promotes surfactant-mediated triglyceride removal from a hydrophobic surface at or below room temperature DOI: 10.1021/am300560z
  • A NEW TARGET FOR MODULATING HUMAN ARTERY FUNCTION: CALCIUM-INDEPENDENT PHOSPHOLIPASE A2B MODULATES RECEPTOR-MEDIATED CONTRACTION
  • Calcium-independent phospholipase A2-beta modulates receptor-mediated contraction in human internal mammary arteries ISSN: 0195-668X
  • EXAMINING THE INTERSECTION BETWEEN NETWORK PHARMACOLOGY AND PERSONALIZING MEDICINES
  • Using the Man9(GlcNAc)2-DC-SIGN pairing to probe specificity in photochemical immobilization DOI: 10.1039/c0mb00118j
  • Personalized medicine: The impact on chemistry DOI: 10.4155/tde.10.64
  • Apparent non-statistical binding in a ditopic receptor for guanosine DOI: 10.1039/b812969j
  • Cover Picture: Rapid Identification of a Putative Interaction between β2-Adrenoreceptor Agonists and ATF4 using a Chemical Genomics Approach (ChemMedChem 5/2008) DOI: 10.1002/cmdc.200890018
  • Rapid identification of a putative interaction between β2- adrenoreceptor agonists and ATF4 using a chemical genomics approach DOI: 10.1002/cmdc.200700317
  • A photoimmobilisation strategy that maximises exploration of chemical space in small molecule affinity selection and target discovery DOI: 10.1039/b704271j
  • Function and stability of abscisic acid acyl hydrazone conjugates by LC-MS2 of ex vivo samples DOI: 10.1021/bc070069x
  • BIOL 114 - Enantiomerically pure abscisic acid conjugates for use in chemical genomics
  • Concise enantioselective synthesis of abscisic acid and a new analogue DOI: 10.1039/b611880a
  • Novel tertiary amine oxide surfaces that resist nonspecific protein adsorption DOI: 10.1021/la060743j
  • Practical syntheses of [1,3,5]-triazine dendritic molecules on solid supports DOI: 10.1002/pola.21336
  • Polymer-supported bifunctional reagents for catalysis.
  • Synthesis and characterisation of new ditopic receptors for guanosine DOI: 10.1016/S0040-4020(03)00708-7
  • Synthesis of novel nucleo-β-amino acids and nucleobase-functionalized β-peptides EID: 2-s2.0-0141504444
  • Interfacing supramolecular and macromolecular chemistry: Metallo-supramolecular triple-helicates incorporated into polymer networks DOI: 10.1039/b210019c
  • High-loading scavenger resins for combinatorial chemistry EID: 2-s2.0-0035862691
  • Atom transfer polymerization: Use of uridine and adenosine derivatized monomers and initiators EID: 2-s2.0-0033748707
  • Copper(I) mediated radical polymerisation of uridine and adenosine monomers on a silica support EID: 2-s2.0-0034619609
  • Determination of the ionization state of 11-thioundecyl-1-phosphonic acid in self-assembled monolayers by chemical force microscopy EID: 2-s2.0-0034193534
  • Improved preparation and application of poly(ethylene glycol) vinyl sulfone EID: 2-s2.0-0034130878
  • Novel polymers from atom transfer polymerisation mediated by copper(I) Schiff base complexes EID: 2-s2.0-0033674547
  • The effect of electrolyte concentration on the chemical force titration behavior of ω-functionalized SAMs: Evidence for the formation of strong ionic hydrogen bonds EID: 2-s2.0-0034269896
  • Atom transfer polymerization: Use of uridine and adenosine derivatized monomers and initiators DOI: 10.1021/ma991438q
  • Hydrogen bond template-directed polymerisation of protected 5′-acryloylnucleosides EID: 2-s2.0-0032677659
  • Hydrogen bond template-directed polymerization of protected 5'-acryloylnucleosides EID: 2-s2.0-0032595934
  • 5 Heterocyclic chemistry EID: 2-s2.0-0343811520
  • Attenuated total reflection fourier transform infrared spectroscopic characterization of fluid lipid bilayers tethered to solid supports EID: 2-s2.0-0032003366
  • Kinetics of formation of single phospholipid bilayers on self-assembled monolayer supports, as monitored by surface plasmon resonance DOI: 10.1016/S0968-5677(97)00036-9
  • Kinetics of the unrolling of small unilamellar phospholipid vesicles onto self-assembled monolayers EID: 2-s2.0-0000679037
  • The design and synthesis of simple molecular tethers for binding biomembranes to a gold surface DOI: 10.1016/S0040-4020(97)00698-4
  • Self-complementary hydrogen bonding heterocycles designed for the enforced self-assembly into supramolecular macrocycles EID: 2-s2.0-0002074298
  • Vitamin D3 synthetic studies. Intramolecular Diels-Alder approaches to the CD-ring fragment DOI: 10.1016/0040-4020(96)00147-0
  • Mesoscopic supramolecular assembly of a 'Janus' molecule and a melamine derivative via complementary hydrogen bonds DOI: 10.1039/C39950002103
  • Janus molecules: Synthesis of double-headed heterocycles containing two identical hydrogen bonding arrays EID: 2-s2.0-0028155981
  • Vitamin-D3-Synthesestudien: enantiospezifische Synthese des CD-Ring-Fragmentes von Vitamin D3 DOI: 10.1002/ange.19931051018
  • Vitamin D3 synthetic studies: Enantiospecific synthesis of the CD ring fragment EID: 2-s2.0-33748218921
  • Intramolecular diels-alder reactions of sulphonyl-substituted trienes DOI: 10.1016/S0040-4020(01)96038-7
  • An Improved Method for the Preparation of Vinylic Sulphoxides DOI: 10.1055/s-1990-21155
  • An unexpected aromatic SN2′ substitution of a 4-bromobenzopyran DOI: 10.1039/C39890001258

Andrew's public data

I-LM-1A_HRMS
2016-09-08T09:32:40Z
I-LM-1A-HMQC
2016-09-08T09:31:09Z
I-LM-1A-HMBC
2016-09-08T09:30:57Z