Year |
Citation |
Score |
2024 |
Gauthier M, Whittingham JBM, Hasija A, Tetlow DJ, Leigh DA. Skeletal Editing of Mechanically Interlocked Molecules: Nitrogen Atom Deletion from Crown Ether-Dibenzylammonium Rotaxanes. Journal of the American Chemical Society. PMID 39431981 DOI: 10.1021/jacs.4c09066 |
0.504 |
|
2023 |
Baluna AS, Dommaschk M, Groh B, Kassem S, Leigh DA, Tetlow DJ, Thomas D, Varela López L. Switched "On" Transient Fluorescence Output from a Pulsed-Fuel Molecular Ratchet. Journal of the American Chemical Society. PMID 38047919 DOI: 10.1021/jacs.3c11290 |
0.41 |
|
2023 |
Baluna AS, Galan A, Leigh DA, Smith GD, Spence JTJ, Tetlow DJ, Vitorica-Yrezabal IJ, Zhang M. In Search of Wasserman's Catenane. Journal of the American Chemical Society. PMID 37096971 DOI: 10.1021/jacs.3c01939 |
0.459 |
|
2022 |
Ren Y, Jamagne R, Tetlow DJ, Leigh DA. A tape-reading molecular ratchet. Nature. PMID 36261530 DOI: 10.1038/s41586-022-05305-9 |
0.419 |
|
2022 |
Thomas D, Tetlow DJ, Ren Y, Kassem S, Karaca U, Leigh DA. Pumping between phases with a pulsed-fuel molecular ratchet. Nature Nanotechnology. PMID 35379944 DOI: 10.1038/s41565-022-01097-1 |
0.419 |
|
2021 |
Echavarren J, Gall MAY, Haertsch A, Leigh DA, Spence JTJ, Tetlow DJ, Tian C. Sequence-Selective Decapeptide Synthesis by the Parallel Operation of Two Artificial Molecular Machines. Journal of the American Chemical Society. PMID 33764775 DOI: 10.1021/jacs.1c01234 |
0.44 |
|
2020 |
Kassem S, Lee ATL, Leigh DA, Markevicius A, Tetlow DJ, Toriumi N. Site-to-site peptide transport on a molecular platform using a small-molecule robotic arm. Chemical Science. 12: 2065-2070. PMID 34163969 DOI: 10.1039/d0sc05906d |
0.547 |
|
2019 |
Echavarren J, Gall MAY, Haertsch A, Leigh DA, Marcos V, Tetlow DJ. Active template rotaxane synthesis through the Ni-catalyzed cross-coupling of alkylzinc reagents with redox-active esters. Chemical Science. 10: 7269-7273. PMID 31588296 DOI: 10.1039/C9Sc02457C |
0.527 |
|
2018 |
Leigh D, Pirvu L, Schaufelberger F, Tetlow DJ, Zhang L. Securing a Supramolecular Architecture By Tying a Stopper Knot. Angewandte Chemie (International Ed. in English). PMID 29708636 DOI: 10.1002/Anie.201803871 |
0.46 |
|
2018 |
Leigh DA, Pirvu L, Schaufelberger F, Tetlow DJ, Zhang L. Frontispiz: Securing a Supramolecular Architecture by Tying a Stopper Knot Angewandte Chemie. 130. DOI: 10.1002/Ange.201883361 |
0.416 |
|
2017 |
Erbas-Cakmak S, Fielden SDP, Karaca U, Leigh DA, McTernan CT, Tetlow DJ, Wilson MR. Rotary and linear molecular motors driven by pulses of a chemical fuel. Science (New York, N.Y.). 358: 340-343. PMID 29051374 DOI: 10.1126/Science.Aao1377 |
0.447 |
|
2017 |
De Bo G, Gall M, Kitching MO, Kuschel S, Leigh DA, Tetlow DJ, Ward JW. Sequence-Specific Beta-Peptide Synthesis by a Rotaxane-Based Molecular Machine. Journal of the American Chemical Society. PMID 28723130 DOI: 10.1021/Jacs.7B05850 |
0.576 |
|
2016 |
Tetlow DJ, Winder SJ, Aïssa C. The synthesis and biological evaluation of a kabiramide C fragment modified with a WH2 consensus actin-binding motif as a potential disruptor of the actin cytoskeleton. Chemical Communications (Cambridge, England). 52: 807-10. PMID 26571306 DOI: 10.1039/C5Cc06081H |
0.622 |
|
2014 |
Aïssa C, Ho KY, Tetlow DJ, Pin-Nó M. Diastereoselective carbocyclization of 1,6-heptadienes triggered by rhodium-catalyzed activation of an olefinic C-H bond. Angewandte Chemie (International Ed. in English). 53: 4209-12. PMID 24634225 DOI: 10.1002/Anie.201400080 |
0.678 |
|
2014 |
Tait MB, Ottersbach PA, Tetlow DJ, Clayden J. Synthesis of 1-arylcycloalkenamines by intramolecular arylation of lithiated ureas Organic Process Research and Development. 18: 1245-1252. DOI: 10.1021/Op500173Q |
0.587 |
|
2013 |
Aïssa C, Crépin D, Tetlow DJ, Ho KY. Multiple rhodium-catalyzed cleavages of single C-C bonds. Organic Letters. 15: 1322-5. PMID 23441873 DOI: 10.1021/Ol400266G |
0.69 |
|
2013 |
Tetlow DJ, Vincent MA, Hillier IH, Clayden J. Reversible aryl migrations in metallated ureas: controlled inversion of configuration at a quaternary carbon atom. Chemical Communications (Cambridge, England). 49: 1548-50. PMID 23324729 DOI: 10.1039/C2Cc38704B |
0.593 |
|
2011 |
Clayden J, Donnard M, Lefranc J, Tetlow DJ. Quaternary centres bearing nitrogen (α-tertiary amines) as products of molecular rearrangements. Chemical Communications (Cambridge, England). 47: 4624-39. PMID 21380444 DOI: 10.1039/C1Cc00049G |
0.691 |
|
2011 |
Lefranc J, Tetlow DJ, Donnard M, Minassi A, Gálvez E, Clayden J. Geometry-selective synthesis of E or Z N-vinyl ureas (N-carbamoyl enamines). Organic Letters. 13: 296-9. PMID 21166427 DOI: 10.1021/Ol1027442 |
0.707 |
|
2011 |
Lefranc J, Tetlow DJ, Donnard M, Minassi A, Galvez E, Clayden J. ChemInform Abstract: Geometry-Selective Synthesis of (E) or (Z) N-Vinyl Ureas (N-Carbamoyl Enamines). Cheminform. 42: no-no. DOI: 10.1002/chin.201115096 |
0.684 |
|
2010 |
Tetlow DJ, Hennecke U, Raftery J, Waring MJ, Clarke DS, Clayden J. Sequential double α-arylation of N-allylureas by asymmetric deprotonation and N→C aryl migration. Organic Letters. 12: 5442-5. PMID 21062018 DOI: 10.1021/Ol102155H |
0.722 |
|
2010 |
Clayden J, Donnard M, Lefranc J, Minassi A, Tetlow DJ. Tandem beta-alkylation-alpha-arylation of amines by carbolithiation and rearrangement of N-carbamoyl enamines (vinyl ureas). Journal of the American Chemical Society. 132: 6624-5. PMID 20411935 DOI: 10.1021/Ja1007992 |
0.715 |
|
2010 |
Clayden J, Donnard M, Lefranc J, Minassi A, Tetlow DJ. N-C Aryl Transfer via Umpolung Carbolithiation ofVinyl Ureas Synfacts. 2010: 929-929. DOI: 10.1055/S-0030-1257749 |
0.548 |
|
2009 |
Clayden J, Farnaby W, Grainger DM, Hennecke U, Mancinelli M, Tetlow DJ, Hillier IH, Vincent MA. N to C aryl migration in lithiated carbamates: alpha-arylation of benzylic alcohols. Journal of the American Chemical Society. 131: 3410-1. PMID 19275248 DOI: 10.1021/Ja808959E |
0.698 |
|
2009 |
Clayden J, Farnaby W, Grainger DM, Hennecke U, Mancinelli M, Tetlow DJ, Hillier IH, Vincent MA. ChemInform Abstract: N to C Aryl Migration in Lithiated Carbamates: α-Arylation of Benzylic Alcohols. Cheminform. 40. DOI: 10.1002/CHIN.200929036 |
0.501 |
|
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