Year |
Citation |
Score |
2023 |
Walsh MP, Barclay JA, Begg CS, Xuan J, Kitching MO. Conglomerate Crystallization in the Cambridge Structural Database (2020-2021). Crystal Growth & Design. 23: 2837-2844. PMID 37038395 DOI: 10.1021/acs.cgd.3c00019 |
0.428 |
|
2022 |
Walsh MP, Barclay JA, Begg CS, Xuan J, Johnson NT, Cole JC, Kitching MO. Identifying a Hidden Conglomerate Chiral Pool in the CSD. Jacs Au. 2: 2235-2250. PMID 36311827 DOI: 10.1021/jacsau.2c00394 |
0.471 |
|
2021 |
Walsh MP, Phelps JM, Lennon ME, Yufit DS, Kitching MO. Enantioselective synthesis of ammonium cations. Nature. 597: 70-76. PMID 34471272 DOI: 10.1038/s41586-021-03735-5 |
0.524 |
|
2020 |
Deichert JA, Mizufune H, Patel JJ, Hurst TE, Maheta A, Kitching M, Ross A, Snieckus V. Expedient Pd‐Catalyzed α‐Arylation towards Dibenzoxepinones: Pivotal Manske's Ketone for the Formal Synthesis of Cularine Alkaloids European Journal of Organic Chemistry. 2020: 4693-4697. DOI: 10.1002/Ejoc.202000424 |
0.398 |
|
2019 |
Snieckus V, Patel J, Kitching M, Dalziel M, Cosman J, Kaye M. The Directed Metalation Group Dance. Regioselective Iterative Functionalization of 7-Azaindole by Controlled Annular Isomerism. Angewandte Chemie (International Ed. in English). PMID 30875442 DOI: 10.1002/Anie.201901724 |
0.398 |
|
2018 |
Snieckus V, Kitching M, Laars M, Board J, Patel J, Gan W. Directed Remote Lateral Metalation: Highly Substituted 2-Naphthols and BINOLs by in situ Directing Group Generation. Angewandte Chemie (International Ed. in English). PMID 29847003 DOI: 10.1002/Anie.201805203 |
0.512 |
|
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 |
0.706 |
|
2017 |
Kitching MO, Dixon OE, Baumann M, Baxendale IR. Flow-Assisted Synthesis: A Key Fragment of SR 142948A European Journal of Organic Chemistry. 2017: 6540-6553. DOI: 10.1002/Ejoc.201700904 |
0.322 |
|
2016 |
Gil-Ramirez G, Hoekman S, Kitching MO, Leigh DA, Vitorica-Yrezabal IJ, Zhang G. Tying a Molecular Overhand Knot of Single Handedness and Asymmetric Catalysis with the Corresponding Pseudo-D3-Symmetric Trefoil Knot. Journal of the American Chemical Society. PMID 27667319 DOI: 10.1021/Jacs.6B08421 |
0.72 |
|
2015 |
Hoekman S, Kitching MO, Leigh DA, Papmeyer M, Roke D. Goldberg Active Template Synthesis of a [2]Rotaxane Ligand for Asymmetric Transition-Metal Catalysis. Journal of the American Chemical Society. 137: 7656-9. PMID 26061430 DOI: 10.1021/Jacs.5B04726 |
0.576 |
|
2015 |
Snieckus V, Hurst T, Kitching M, da Frota L, Guimarães K, Dalziel M. Metal-Free Synthesis of Dibenzoxazepinones via a One-Pot SNAr and Smiles Rearrangement Process: Orthogonality with Copper-Catalyzed Cyclizations Synlett. 26: 1455-1460. DOI: 10.1055/S-0034-1378839 |
0.449 |
|
2015 |
Hurst TE, Kitching MO, da Frota LCRM, Guimaraes KG, Dalziel ME, Snieckus V. ChemInform Abstract: Metal-Free Synthesis of Dibenzoxazepinones via a One-Pot SNAr and Smiles Rearrangement Process: Orthogonality with Copper-Catalyzed Cyclizations. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201545193 |
0.398 |
|
2013 |
Baxendale IR, Cheung S, Kitching MO, Ley SV, Shearman JW. The synthesis of neurotensin antagonist SR 48692 for prostate cancer research. Bioorganic & Medicinal Chemistry. 21: 4378-87. PMID 23721919 DOI: 10.1016/J.Bmc.2013.04.075 |
0.446 |
|
2013 |
Battilocchio C, Deadman BJ, Nikbin N, Kitching MO, Baxendale IR, Ley SV. A machine-assisted flow synthesis of SR48692: a probe for the investigation of neurotensin receptor-1. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 7917-30. PMID 23592596 DOI: 10.1002/Chem.201300696 |
0.666 |
|
2013 |
Snieckus V, Kitching MO. Rhodium-Catalyzed Annulation Route to Heterocyclic MIDA Boronates Synfacts. 9: 261-261. DOI: 10.1055/S-0032-1318288 |
0.497 |
|
2013 |
Snieckus V, Kitching MO. N-Heterocyclic Carbene Catalyzed Synthesis of Enantioenriched Lactones Synfacts. 9: 260-260. DOI: 10.1055/S-0032-1318287 |
0.479 |
|
2013 |
Snieckus V, Kitching MO. Palladium-Catalyzed Synthesis of Benzo[b][1,4]oxazepines Synfacts. 9: 30-30. DOI: 10.1055/S-0032-1317878 |
0.466 |
|
2013 |
Snieckus V, Kitching MO. Isatoic Anhydrides via C–H Activation Synfacts. 9: 19-19. DOI: 10.1055/S-0032-1317877 |
0.335 |
|
2012 |
Kitching MO, Snieckus V. Organic chemistry: Directors extend their reach. Nature. 486: 478-9. PMID 22739310 DOI: 10.1038/486478A |
0.427 |
|
2012 |
Johansson Seechurn CC, Kitching MO, Colacot TJ, Snieckus V. Palladium-catalyzed cross-coupling: a historical contextual perspective to the 2010 Nobel Prize. Angewandte Chemie (International Ed. in English). 51: 5062-85. PMID 22573393 DOI: 10.1002/Anie.201107017 |
0.438 |
|
2012 |
Kitching MO, Hurst TE, Snieckus V. Copper-catalyzed cross-coupling interrupted by an opportunistic Smiles rearrangement: an efficient domino approach to dibenzoxazepinones. Angewandte Chemie (International Ed. in English). 51: 2925-9. PMID 22311826 DOI: 10.1002/Anie.201106786 |
0.414 |
|
2012 |
Snieckus V, Kitching MO. Rhodium-Catalyzed Synthesis of 3-Aryl Indoles from 1-Sulfonyl 1,2,3-Triazoles Synfacts. 8: 1298-1298. DOI: 10.1055/S-0032-1317658 |
0.546 |
|
2012 |
Snieckus V, Kitching MO. Palladium-Catalyzed Cyclization of Electron-Deficient Enynes Synfacts. 8: 1295-1295. DOI: 10.1055/S-0032-1317657 |
0.409 |
|
2012 |
Snieckus V, Kitching MO. Copper-Catalyzed Oxytrifluoromethylation of Alkenes to Oxygenated Heterocycles Synfacts. 8: 1069-1069. DOI: 10.1055/S-0032-1317289 |
0.39 |
|
2012 |
Snieckus V, Kitching MO. Palladium-Catalyzed Synthesis of Quinolines Synfacts. 8: 947-947. DOI: 10.1055/S-0032-1317125 |
0.542 |
|
2012 |
Snieckus V, Kitching MO. Gold-Catalyzed Cyclizations Leading to Indenoazepines and Strained Bicycles Synfacts. 8: 952-952. DOI: 10.1055/S-0032-1317124 |
0.38 |
|
2012 |
Snieckus V, Kitching MO. Indoloazocines via a Sequential Ugi–Gold-Catalyzed Hydroarylation Synfacts. 8: 839-839. DOI: 10.1055/S-0032-1316700 |
0.486 |
|
2012 |
Snieckus V, Kitching MO. Selectivity in Palladium-Catalyzed Carboesterification – Amides versus Esters Synfacts. 8: 836-836. DOI: 10.1055/S-0032-1316699 |
0.437 |
|
2012 |
Snieckus V, Kitching MO. Enantioselective Synthesis of γ-Butyro-lactones via Dynamic Kinetic Resolution Synfacts. 8: 719-719. DOI: 10.1055/S-0032-1316526 |
0.448 |
|
2012 |
Snieckus V, Kitching MO. Ruthenium-Catalyzed Dehydrative Benzofuran Synthesis via C–H Activation Synfacts. 8: 713-713. DOI: 10.1055/S-0032-1316516 |
0.509 |
|
2012 |
Snieckus V, Kitching MO, He C, Guo S, Ke J, Hao J, Xu H, Chen H, Lei A. Silver-Mediated Dual C–H/C–H Activation for the Synthesis of 3-Acyl Furans Synfacts. 8: 608-608. DOI: 10.1055/S-0031-1291078 |
0.479 |
|
2012 |
Snieckus V, Kitching MO. Synthesis of 4-Aryl-2-quinolinone by a Tandem Heck/C–H Amidation Approach Synfacts. 8: 601-601. DOI: 10.1055/S-0031-1291077 |
0.493 |
|
2012 |
Snieckus V, Kitching MO. Convergent Domino Oxidation for Oxazole Synthesis Synfacts. 8: 488-488. DOI: 10.1055/S-0031-1290854 |
0.43 |
|
2012 |
Snieckus V, Kitching MO. Synthesis of Oxindoles via Intramolecular Enantioselective α-Arylation Synfacts. 8: 483-483. DOI: 10.1055/S-0031-1290853 |
0.475 |
|
2012 |
Snieckus V, Kitching MO. A Domino Radical Smiles Rearrangement Approach to Indolin-2-ones Synfacts. 8: 375-375. DOI: 10.1055/S-0031-1290744 |
0.347 |
|
2012 |
Snieckus V, Kitching MO, Wei L, Zhang J. Synthesis of Isochromanones and Isoquinolines via Friedel–Crafts Cyclization Synfacts. 8: 371-371. DOI: 10.1055/S-0031-1290743 |
0.526 |
|
2012 |
Snieckus V, Kitching MO. Oxidative Expansion of Oxiranes and Oxetanes via Copper Catalysis Synfacts. 8: 257-257. DOI: 10.1055/S-0031-1290299 |
0.365 |
|
2012 |
Snieckus V, Kitching MO. Synthesis of Nitrated Triazoles as Potentially New Explosives Synfacts. 8: 256-256. DOI: 10.1055/S-0031-1290298 |
0.462 |
|
2012 |
Snieckus V, Kitching MO. (Pyrazolo)pyrimidines/Purines via a Three- Component Reaction Synfacts. 8: 133-133. DOI: 10.1055/S-0031-1290154 |
0.398 |
|
2012 |
Snieckus V, Kitching MO. Three-Component Synthesis of Pyrazoles Using Titanium Catalysis Synfacts. 8: 147-147. DOI: 10.1055/S-0031-1290151 |
0.466 |
|
2012 |
Snieckus V, Kitching MO. Intramolecular Heck-Type Synthesis of Piperideines and Pyridines Synfacts. 8: 25-25. DOI: 10.1055/S-0031-1289954 |
0.478 |
|
2012 |
Snieckus V, Kitching MO. Phthalimide Synthesis via Oxidative Carbonylation of Benzamides Synfacts. 8: 19-19. DOI: 10.1055/S-0031-1289953 |
0.437 |
|
2012 |
Battilocchio C, Baumann M, Baxendale IR, Biava M, Kitching MO, Ley SV, Martin RE, Ohnmacht SA, Tappin NDC. Scale-up of flow-assisted synthesis of C 2-symmetric chiral PyBox ligands Synthesis. 44: 635-647. DOI: 10.1055/S-0031-1289676 |
0.674 |
|
2012 |
Battilocchio C, Baxendale IR, Biava M, Kitching MO, Ley SV. A flow-based synthesis of 2-aminoadamantane-2-carboxylic acid Organic Process Research and Development. 16: 798-810. DOI: 10.1021/Op300084Z |
0.688 |
|
2012 |
Johansson Seechurn CCC, Kitching MO, Colacot TJ, Snieckus V. Palladiumkatalysierte Kreuzkupplungen: eine historische Perspektive im Kontext der Nobel-Preise 2010 Angewandte Chemie. 124: 5150-5174. DOI: 10.1002/Ange.201107017 |
0.369 |
|
2010 |
Tozzi F, Ley SV, Kitching MO, Baxendale IR. Enzymatic oxidative cyclisation reactions leading to dibenzoazocanes Synlett. 1919-1922. DOI: 10.1055/S-0030-1258486 |
0.419 |
|
2009 |
Myers RM, Shearman JW, Kitching MO, Ramos-Montoya A, Neal DE, Ley SV. Cancer, chemistry, and the cell: molecules that interact with the neurotensin receptors. Acs Chemical Biology. 4: 503-25. PMID 19462983 DOI: 10.1021/Cb900038E |
0.651 |
|
2008 |
Åberg G, Aigbirhio FI, Alexakis E, Al-Maharik N, Almi M, Ambacher Y, Andersson S, Athlan A, Badman G, Baldwin SA, Baumann M, Baxendale IR, Botting NP, Bragg RA, Brown JA, ... ... Kitching MO, et al. 16th International Isotope Society (UK group) Symposium Journal of Labelled Compounds and Radiopharmaceuticals. 51: 247-261. DOI: 10.1002/Jlcr.1513 |
0.326 |
|
2008 |
Aureggi V, Franckevičius V, Kitching MO, Ley SV, Longbottom DA, Oelke AJ, Sedelmeier G. (S)‐5‐Pyrrolidin‐2‐Yl‐1H‐Tetrazole Organic Syntheses. 72-87. DOI: 10.1002/0471264229.Os085.09 |
0.447 |
|
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