| Year |
Citation |
Score |
| 2022 |
Lovelock SL, Crawshaw R, Basler S, Levy C, Baker D, Hilvert D, Green AP. The road to fully programmable protein catalysis. Nature. 606: 49-58. PMID 35650353 DOI: 10.1038/s41586-022-04456-z |
0.48 |
|
| 2021 |
Crawshaw R, Crossley AE, Johannissen L, Burke AJ, Hay S, Levy C, Baker D, Lovelock SL, Green AP. Engineering an efficient and enantioselective enzyme for the Morita-Baylis-Hillman reaction. Nature Chemistry. PMID 34916595 DOI: 10.1038/s41557-021-00833-9 |
0.309 |
|
| 2021 |
Bulmer GS, Mattey AP, Parmeggiani F, Williams R, Ledru H, Marchesi A, Seibt LS, Both P, Huang K, Galan MC, Flitsch SL, Green AP, van Munster JM. A promiscuous glycosyltransferase generates poly-β-1,4-glucan derivatives that facilitate mass spectrometry-based detection of cellulolytic enzymes. Organic & Biomolecular Chemistry. PMID 34105582 DOI: 10.1039/d1ob00971k |
0.493 |
|
| 2020 |
Ortmayer M, Fisher K, Basran J, Wolde-Michael EM, Heyes DJ, Levy C, Lovelock SL, Anderson JLR, Raven EL, Hay S, Rigby SEJ, Green AP. Rewiring the "Push-Pull" Catalytic Machinery of a Heme Enzyme Using an Expanded Genetic Code. Acs Catalysis. 10: 2735-2746. PMID 32550044 DOI: 10.1021/Acscatal.9B05129 |
0.349 |
|
| 2020 |
Zhao J, Burke AJ, Green AP. Enzymes with noncanonical amino acids. Current Opinion in Chemical Biology. 55: 136-144. PMID 32163871 DOI: 10.1016/J.Cbpa.2020.01.006 |
0.336 |
|
| 2020 |
Paggiola G, Derrien N, Moseley JD, Green A, Flitsch SL, Clark JH, McElroy CR, Hunt AJ. Application of bio-based solvents for biocatalysed synthesis of amides with Pseudomonas stutzeri lipase (PSL) Pure and Applied Chemistry. 92: 579-586. DOI: 10.1515/Pac-2019-0808 |
0.535 |
|
| 2019 |
Burke AJ, Lovelock SL, Frese A, Crawshaw R, Ortmayer M, Dunstan M, Levy C, Green AP. Design and evolution of an enzyme with a non-canonical organocatalytic mechanism. Nature. PMID 31132786 DOI: 10.1038/S41586-019-1262-8 |
0.395 |
|
| 2018 |
Turner NJ, Green A, Xu J. Chemo-enzymatic synthesis of pyrazines and pyrroles. Angewandte Chemie (International Ed. in English). PMID 30335228 DOI: 10.1002/Anie.201810555 |
0.325 |
|
| 2018 |
Hayashi T, Hilvert D, Green AP. Engineered Metalloenzymes with Non-Canonical Coordination Environments. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29786902 DOI: 10.1002/Chem.201800975 |
0.54 |
|
| 2018 |
Pott M, Hayashi T, Mori T, Mittl PRE, Green AP, Hilvert D. A Non-Canonical Proximal Heme Ligand Affords an Efficient Peroxidase in a Globin Fold. Journal of the American Chemical Society. PMID 29309143 DOI: 10.1021/Jacs.7B12621 |
0.544 |
|
| 2018 |
Hayashi T, Hilvert D, Green AP. Frontispiece: Engineered Metalloenzymes with Non‐Canonical Coordination Environments Chemistry – a European Journal. 24. DOI: 10.1002/Chem.201884661 |
0.46 |
|
| 2017 |
Green AP, Hardy S, Lee ATL, Thomas EJ. Total synthesis of 7-des-O-pivaloyl-7-O-benzylbryostatin 10. Organic & Biomolecular Chemistry. PMID 29109995 DOI: 10.1039/C7Ob02129A |
0.318 |
|
| 2017 |
Gray CJ, Schindler B, Migas LG, Picmanova M, Allouche AR, Green AP, Mandal S, Motawia MS, Sánchez-Pérez R, Bjarnholt N, Møller BL, Rijs AM, Barran PE, Compagnon I, Eyers CE, et al. Bottom-up elucidation of glycosidic bond stereochemistry. Analytical Chemistry. PMID 28350444 DOI: 10.1021/Acs.Analchem.6B04998 |
0.517 |
|
| 2016 |
Green AP, Hayashi T, Mittl PR, Hilvert D. A Chemically Programmed Proximal Ligand Enhances the Catalytic Properties of a Heme Enzyme. Journal of the American Chemical Society. PMID 27500802 DOI: 10.1021/Jacs.6B07029 |
0.557 |
|
| 2016 |
Gomm A, Lewis W, Green AP, O'Reilly E. A new generation of smart amine donors for transaminase-mediated biotransformations. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27411957 DOI: 10.1002/Chem.201603188 |
0.354 |
|
| 2016 |
Green AP, Turner NJ. Biocatalytic retrosynthesis: Redesigning synthetic routes to high-value chemicals Perspectives in Science. 9: 42-48. DOI: 10.1016/J.Pisc.2016.04.106 |
0.401 |
|
| 2014 |
Green AP, Turner NJ, O'Reilly E. Chiral amine synthesis using ω-transaminases: an amine donor that displaces equilibria and enables high-throughput screening. Angewandte Chemie (International Ed. in English). 53: 10714-7. PMID 25138082 DOI: 10.1002/Anie.201406571 |
0.347 |
|
| 2014 |
Both P, Green AP, Gray CJ, SardzÃk R, Voglmeir J, Fontana C, Austeri M, Rejzek M, Richardson D, Field RA, Widmalm G, Flitsch SL, Eyers CE. Discrimination of epimeric glycans and glycopeptides using IM-MS and its potential for carbohydrate sequencing. Nature Chemistry. 6: 65-74. PMID 24345949 DOI: 10.1038/Nchem.1817 |
0.617 |
|
| 2013 |
Ghislieri D, Green AP, Pontini M, Willies SC, Rowles I, Frank A, Grogan G, Turner NJ. Engineering an enantioselective amine oxidase for the synthesis of pharmaceutical building blocks and alkaloid natural products. Journal of the American Chemical Society. 135: 10863-9. PMID 23808566 DOI: 10.1021/Ja4051235 |
0.378 |
|
| 2013 |
Ghislieri D, Houghton D, Green AP, Willies SC, Turner NJ. Monoamine oxidase (MAO-N) catalyzed deracemization of tetrahydro-β- carbolines: Substrate dependent switch in enantioselectivity Acs Catalysis. 3: 2869-2872. DOI: 10.1021/Cs400724G |
0.363 |
|
| 2012 |
Šardzík R, Green AP, Laurent N, Both P, Fontana C, Voglmeir J, Weissenborn MJ, Haddoub R, Grassi P, Haslam SM, Widmalm G, Flitsch SL. Chemoenzymatic synthesis of O-mannosylpeptides in solution and on solid phase. Journal of the American Chemical Society. 134: 4521-4. PMID 22372538 DOI: 10.1021/Ja211861M |
0.616 |
|
| 2011 |
Green AP, Lee AT, Thomas EJ. Total synthesis of a 20-deoxybryostatin. Chemical Communications (Cambridge, England). 47: 7200-2. PMID 21614401 DOI: 10.1039/C1Cc12332G |
0.303 |
|
| 2010 |
Green AP, Hardy S, Lee ATL, Thomas EJ. Approaches to the total synthesis of biologically active natural products: Studies directed towards bryostatins Phytochemistry Reviews. 9: 501-513. DOI: 10.1007/S11101-010-9186-9 |
0.335 |
|
| 2008 |
Allen JV, Green AP, Hardy S, Heron NM, Lee ATL, Thomas EJ. On the use of the modified Julia olefination for bryostatin synthesis Tetrahedron Letters. 49: 6352-6355. DOI: 10.1016/J.Tetlet.2008.08.075 |
0.308 |
|
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