Matthew O. Kitching - Publications

Affiliations: 
Chemistry Durham University, Durham, England, United Kingdom 

49 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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  0.43
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  0.472
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  0.525
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  0.71
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  0.722
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  0.397
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  0.478
2013 Snieckus V, Kitching MO. Palladium-Catalyzed Synthesis of Benzo[b][1,4]oxazepines Synfacts. 9: 30-30. DOI: 10.1055/S-0032-1317878  0.465
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  0.545
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  0.389
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  0.379
2012 Snieckus V, Kitching MO. Indoloazocines via a Sequential Ugi–Gold-Catalyzed Hydroarylation Synfacts. 8: 839-839. DOI: 10.1055/S-0032-1316700  0.485
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  0.447
2012 Snieckus V, Kitching MO. Ruthenium-Catalyzed Dehydrative Benzofuran Synthesis via C–H Activation Synfacts. 8: 713-713. DOI: 10.1055/S-0032-1316516  0.508
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  0.492
2012 Snieckus V, Kitching MO. Convergent Domino Oxidation for Oxazole Synthesis Synfacts. 8: 488-488. DOI: 10.1055/S-0031-1290854  0.429
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  0.525
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  0.461
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  0.465
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  0.436
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  0.418
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  0.656
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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