| Year |
Citation |
Score |
| 2019 |
Liu Z, Turyanska L, Zamberlan F, Pacifico S, Bradshaw TD, Moro F, Fay MW, Williams H, Thomas NR. Synthesis of folic acid functionalized gold nanoclusters for targeting folate receptor-positive cells. Nanotechnology. PMID 31509807 DOI: 10.1088/1361-6528/Ab437C |
0.321 |
|
| 2018 |
Strickland M, Tudorica V, Řezáč M, Thomas NR, Goodacre SL. Conservation of a pH-sensitive structure in the C-terminal region of spider silk extends across the entire silk gene family. Heredity. PMID 29445119 DOI: 10.1038/S41437-018-0050-9 |
0.301 |
|
| 2016 |
Harvey D, Bardelang P, Goodacre SL, Cockayne A, Thomas NR. Antibiotic Spider Silk: Site-Specific Functionalization of Recombinant Spider Silk Using "Click" Chemistry. Advanced Materials (Deerfield Beach, Fla.). PMID 28028885 DOI: 10.1002/Adma.201604245 |
0.319 |
|
| 2010 |
Roth S, Drewe WC, Thomas NR. A concise and scalable route to L-azidohomoalanine. Nature Protocols. 5: 1967-73. PMID 21127494 DOI: 10.1038/Nprot.2010.164 |
0.306 |
|
| 2010 |
Partha SK, Sadeghi-Khomami A, Slowski K, Kotake T, Thomas NR, Jakeman DL, Sanders DA. Chemoenzymatic synthesis, inhibition studies, and X-ray crystallographic analysis of the phosphono analog of UDP-Galp as an inhibitor and mechanistic probe for UDP-galactopyranose mutase. Journal of Molecular Biology. 403: 578-90. PMID 20850454 DOI: 10.1016/J.Jmb.2010.08.053 |
0.322 |
|
| 2010 |
Roth S, Thomas NR. A concise route to L-azidoamino acids: L-azidoalanine, L-azidohomo-alanine and L-azidonorvaline Synlett. 607-609. DOI: 10.1055/S-0029-1218391 |
0.333 |
|
| 2009 |
Townsend AP, Roth S, Williams HE, Stylianou E, Thomas NR. New S-adenosyl-L-methionine analogues: synthesis and reactivity studies. Organic Letters. 11: 2976-9. PMID 19552444 DOI: 10.1021/Ol9009859 |
0.311 |
|
| 2009 |
Beaton SA, Huestis MP, Sadeghi-Khomami A, Thomas NR, Jakeman DL. Enzyme-catalyzed synthesis of isosteric phosphono-analogues of sugar nucleotides. Chemical Communications (Cambridge, England). 238-40. PMID 19099081 DOI: 10.1039/B808078J |
0.308 |
|
| 2009 |
Bardelang P, Vankemmelbeke M, Zhang Y, Jarvis H, Antoniadou E, Rochette S, Thomas NR, Penfold CN, James R. Design of a polypeptide FRET substrate that facilitates study of the antimicrobial protease lysostaphin. The Biochemical Journal. 418: 615-24. PMID 19032148 DOI: 10.1042/Bj20081765 |
0.33 |
|
| 2009 |
Benaissi K, Poliakoff M, Thomas NR. Dynamic kinetic resolution of rac-1-phenylethanol in supercritical carbon dioxide Green Chemistry. 11: 617-621. DOI: 10.1039/B822349A |
0.325 |
|
| 2007 |
Kouvatsos N, Thurston V, Ball K, Oldham NJ, Thomas NR, Searle MS. Bile acid interactions with rabbit ileal lipid binding protein and an engineered helixless variant reveal novel ligand binding properties of a versatile beta-clam shell protein scaffold. Journal of Molecular Biology. 371: 1365-77. PMID 17618650 DOI: 10.1016/J.Jmb.2007.06.024 |
0.303 |
|
| 2006 |
Sadeghi-Khomami A, Thomas NR, Wilson C. (±)-exo-2-Hydroxy-5-oxo-4,8-dioxatricyclo[4.2.1.0 3,7]nonane-9-exo-carboxylic acid Acta Crystallographica Section E: Structure Reports Online. 62: o3759-o3761. DOI: 10.1107/S1600536806030649 |
0.303 |
|
| 1997 |
De BB, Thomas NR. Optimisation of the retroracemisation procedure for α-amino acids using (S)-2-[(N-alkylprolyl)amino]benzophenones, recyclable chiral axiliaries Tetrahedron Asymmetry. 8: 2687-2691. DOI: 10.1016/S0957-4166(97)00331-5 |
0.369 |
|
| 1994 |
Stewart JD, Roberts VA, Thomas NR, Getzoff ED, Benkovic SJ. Site-directed mutagenesis of a catalytic antibody: an arginine and a histidine residue play key roles. Biochemistry. 33: 1994-2003. PMID 8117656 DOI: 10.1021/Bi00174A004 |
0.308 |
|
| 1993 |
Thomas NR, Rose JE, Gani D. Decarboxylation of 2-aminomalonic acid by serine hydroxymethyltransferase is, in fact, a stereospecific process J.Chem.Soc.Perkin Trans.1. 2933-2937. DOI: 10.1039/P19930002933 |
0.61 |
|
| 1993 |
Thomas NR, Schirch V, Gani D. Stereochemical course of the decarboxylation of 2-amino-2-methylmalonic acid by serine hydroxymethyltransferase J.Chem.Soc.Perkin Trans.1. 2925-2931. DOI: 10.1039/P19930002925 |
0.631 |
|
| 1993 |
Archer CH, Thomas NR, Gani D. Syntheses of (2S,3R)- and (2S,3R)[3-2h]- 3-methylaspartic acid: slow substrates for a syn-elimination reaction catalysed by methylaspartase. Tetrahedron: Asymmetry. 4: 1141-1152. DOI: 10.1016/S0957-4166(00)80221-9 |
0.598 |
|
| 1993 |
Thomas NR, Schirch V, Gani D. Stereochemical course of the decarboxylation of 2-amino-2-methylmalonic acid by serine hydroxymethyltransferase J.Chem.Soc.Perkin Trans.1. 2925-2931. |
0.574 |
|
| 1993 |
Thomas NR, Rose JE, Gani D. Decarboxylation of 2-aminomalonic acid by serine hydroxymethyltransferase is, in fact, a stereospecific process J.Chem.Soc.Perkin Trans.1. 2933-2937. |
0.559 |
|
| 1991 |
Smith DM, Thomas NR, Gani D. A comparison of pyridoxal 5'-phosphate dependent decarboxylase and transaminase enzymes at a molecular level. Experientia. 47: 1104-18. PMID 1765122 DOI: 10.1007/Bf01918374 |
0.597 |
|
| 1991 |
Thomas NR, Rose JE, Gani D. Decarboxylation of 2-aminomalonic acid catalysed by serine hydroxymethyltransferase is, in fact, a stereospecific process Journal of the Chemical Society, Chemical Communications. 908-909. DOI: 10.1039/C39910000908 |
0.607 |
|
| 1991 |
Thomas NR, Gani D. Synthesis of (2R)- and (2S)- [1-13C]-2-amino-2-methylmalonic acid: Chiral substrates for serine hydroxymethyltransferase Tetrahedron. 47: 497-506. DOI: 10.1016/S0040-4020(01)90505-8 |
0.619 |
|
| 1990 |
Thomas NR, Schirch V, Gani D. Synthesis of (2R)- and (2S)-[1-13C]-2-amino-2-methylmalonic acid, probes for the serine hydroxymethyltransferase reaction: Stereospecific decarboxylation of the 2-pro-R carboxy group with the retention of configuration Journal of the Chemical Society, Chemical Communications. 400-402. DOI: 10.1039/C39900000400 |
0.609 |
|
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