Year |
Citation |
Score |
2023 |
Doherty KE, Sandoval AL, Politano F, Witko ML, Schroeder CM, Brydon WP, Wadey GP, Ohlhorst KK, Leadbeater NE. Scale-up of Sodium Persulfate Mediated, Nitroxide Catalyzed Oxidative Functionalization Reactions. Current Organic Synthesis. PMID 37653636 DOI: 10.2174/1570179421666230831105337 |
0.411 |
|
2023 |
Schroeder CM, Politano F, Ohlhorst KK, Leadbeater NE. Acetamido-TEMPO mediated electrochemical oxidation of alcohols to aldehydes and ketones. Rsc Advances. 13: 25459-25463. PMID 37636515 DOI: 10.1039/d3ra04608g |
0.329 |
|
2022 |
León Sandoval A, Doherty KE, Wadey GP, Leadbeater NE. Solvent- and additive-free oxidative amidation of aldehydes using a recyclable oxoammonium salt. Organic & Biomolecular Chemistry. 20: 2249-2254. PMID 35230379 DOI: 10.1039/d2ob00307d |
0.834 |
|
2022 |
León Sandoval A, Politano F, Witko ML, Leadbeater NE. Preparation of nitriles from aldehydes using ammonium persulfate by means of a nitroxide-catalysed oxidative functionalisation reaction. Organic & Biomolecular Chemistry. 20: 667-671. PMID 34989384 DOI: 10.1039/d1ob02187g |
0.837 |
|
2021 |
León Sandoval A, Politano F, Witko ML, Leadbeater NE. Preparation of hexafluoroisopropyl esters by oxidative esterification of aldehydes using sodium persulfate. Organic & Biomolecular Chemistry. PMID 33734281 DOI: 10.1039/d1ob00251a |
0.824 |
|
2020 |
Nandi J, Vaughan M, Leon Sandoval A, Paolillo J, Leadbeater NE. Oxidative Amidation of Amines in Tandem with Transamidation: A Route to Amides using Visible-Light Energy. The Journal of Organic Chemistry. PMID 32539393 DOI: 10.1021/Acs.Joc.0C01222 |
0.813 |
|
2020 |
Miller SA, Sandoval AL, Leadbeater NE. Oxidation of alcohols using an oxoammonium salt bearing the nitrate anion Tetrahedron Letters. 61: 151464. DOI: 10.1016/J.Tetlet.2019.151464 |
0.612 |
|
2019 |
Politano F, Gran-Magano AK, Leadbeater NE. One-Pot Two-Step Synthesis of 2-Aryl benzimidazole -oxides Using Microwave Heating as a Tool. Molecules (Basel, Switzerland). 24. PMID 31600970 DOI: 10.3390/molecules24203639 |
0.377 |
|
2019 |
Nandi J, Leadbeater NE. Visible-light-driven catalytic oxidation of aldehydes and alcohols to nitriles by 4-acetamido-TEMPO using ammonium carbamate as a nitrogen source. Organic & Biomolecular Chemistry. PMID 31595927 DOI: 10.1039/C9Ob01918A |
0.816 |
|
2019 |
Miller SA, Nandi J, Leadbeater NE, Eddy NA. Probing the Effect of Counterions on the Oxidation of Alcohols Using Oxoammonium Salts European Journal of Organic Chemistry. 2020: 108-112. DOI: 10.1002/Ejoc.201901369 |
0.791 |
|
2018 |
Pistritto VA, Paolillo JM, Bisset KA, Leadbeater NE. Oxidation of α-trifluoromethyl and non-fluorinated alcohols via the merger of oxoammonium cations and photoredox catalysis. Organic & Biomolecular Chemistry. PMID 29900460 DOI: 10.1039/c8ob01063c |
0.342 |
|
2018 |
Leadbeater N, Nandi J, Witko M. Combining Oxoammonium Cation Mediated Oxidation and Photoredox Catalysis for the Conversion of Aldehydes into Nitriles Synlett. 29: 2185-2190. DOI: 10.1055/S-0037-1610272 |
0.835 |
|
2018 |
Miller SA, van Beek B, Hamlin TA, Bickelhaupt FM, Leadbeater NE. A methodology for the photocatalyzed radical trifluoromethylation of indoles: A combined experimental and computational study Journal of Fluorine Chemistry. 214: 94-100. DOI: 10.1016/J.Jfluchem.2018.08.005 |
0.764 |
|
2018 |
Miller SA, Bisset KA, Leadbeater NE, Eddy NA. Catalytic Oxidation of Alcohols Using a 2,2,6,6-Tetramethylpiperidine-N
-hydroxyammonium Cation European Journal of Organic Chemistry. 2019: 1413-1417. DOI: 10.1002/Ejoc.201801718 |
0.557 |
|
2017 |
Nandi J, Ovian JM, Kelly CB, Leadbeater NE. Oxidative functionalisation of alcohols and aldehydes via the merger of oxoammonium cations and photoredox catalysis. Organic & Biomolecular Chemistry. PMID 28929164 DOI: 10.1039/C7Ob02243C |
0.806 |
|
2017 |
Miller SA, Bobbitt JM, Leadbeater NE. Oxidation of terminal diols using an oxoammonium salt: a systematic study. Organic & Biomolecular Chemistry. PMID 28281712 DOI: 10.1039/C7Ob00039A |
0.633 |
|
2017 |
Ovian JM, Kelly CB, Pistritto VA, Leadbeater NE. Accessing N-Acyl Azoles via Oxoammonium Salt-Mediated Oxidative Amidation. Organic Letters. PMID 28248527 DOI: 10.1021/Acs.Orglett.7B00060 |
0.835 |
|
2016 |
Loman JJ, Carnaghan ER, Hamlin TA, Ovian JM, Kelly CB, Mercadante MA, Leadbeater NE. A combined computational and experimental investigation of the oxidative ring-opening of cyclic ethers by oxoammonium cations. Organic & Biomolecular Chemistry. PMID 27031501 DOI: 10.1039/C6Ob00347H |
0.8 |
|
2016 |
Magpusao AN, Rutledge K, Hamlin TA, Lawrence JM, Mercado BQ, Leadbeater NE, Peczuh MW. Rules of Macrocycle Topology: A [13]-Macrodilactone Case Study. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 6001-11. PMID 27001347 DOI: 10.1002/Chem.201504684 |
0.539 |
|
2016 |
Loman JJ, Pistritto VA, Kelly CB, Leadbeater NE. Oxidative Cleavage of Silyl Ethers by an Oxoammonium Salt Synlett. 27: 2372-2377. DOI: 10.1055/S-0035-1561498 |
0.688 |
|
2016 |
Balti M, Miller SA, Efrit ML, Leadbeater NE. An approach to the synthesis of 4-aryl and 5-aryl substituted thiazole-2(3H)-thiones employing flow processing Rsc Advances. 6: 72165-72169. DOI: 10.1039/C6Ra15488C |
0.52 |
|
2015 |
Hamlin TA, Leadbeater NE. Real-time Monitoring of Reactions Performed Using Continuous-flow Processing: The Preparation of 3-Acetylcoumarin as an Example. Journal of Visualized Experiments : Jove. PMID 26650190 DOI: 10.3791/52393 |
0.593 |
|
2015 |
Hamlin TA, Kelly CB, Ovian JM, Wiles RJ, Tilley LJ, Leadbeater NE. Toward a Unified Mechanism for Oxoammonium Salt-Mediated Oxidation Reactions: A Theoretical and Experimental Study Using a Hydride Transfer Model. The Journal of Organic Chemistry. 80: 8150-67. PMID 26167866 DOI: 10.1021/Acs.Joc.5B01240 |
0.814 |
|
2015 |
Kelly CB, Ovian JM, Cywar RM, Gosselin TR, Wiles RJ, Leadbeater NE. Oxidative cleavage of allyl ethers by an oxoammonium salt. Organic & Biomolecular Chemistry. 13: 4255-9. PMID 25748071 DOI: 10.1039/C5Ob00270B |
0.809 |
|
2015 |
Kelly CB, Lambert KM, Mercadante MA, Ovian JM, Bailey WF, Leadbeater NE. Access to nitriles from aldehydes mediated by an oxoammonium salt. Angewandte Chemie (International Ed. in English). 54: 4241-5. PMID 25665019 DOI: 10.1002/Anie.201412256 |
0.832 |
|
2015 |
Miller SA, Leadbeater NE. Direct, rapid, solvent-free conversion of unactivated esters to amides using lithium hydroxide as a catalyst Rsc Advances. 5: 93248-93251. DOI: 10.1039/C5Ra21394K |
0.557 |
|
2015 |
Hamlin TA, Kelly CB, Ovian JM, Wiles RJ, Tilley LJ, Leadbeater NE. Toward a Unified Mechanism for Oxoammonium Salt-Mediated Oxidation Reactions: A Theoretical and Experimental Study Using a Hydride Transfer Model Journal of Organic Chemistry. 80: 8150-8167. DOI: 10.1021/acs.joc.5b01240 |
0.814 |
|
2015 |
Kelly CB, Mercadante MA, Carnaghan ER, Doherty MJ, Fager DC, Hauck JJ, Macinnis AE, Tilley LJ, Leadbeater NE. Synthesis of Perfluoroalkyl-Substituted Vinylcyclopropanes by Way of Enhanced Neighboring Group Participation European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201500565 |
0.803 |
|
2014 |
Hamlin TA, Kelly CB, Cywar RM, Leadbeater NE. Methylenation of perfluoroalkyl ketones using a Peterson olefination approach. The Journal of Organic Chemistry. 79: 1145-55. PMID 24410210 DOI: 10.1021/Jo402577N |
0.825 |
|
2014 |
Mercadante MA, Kelly CB, Hamlin TA, Delle Chiaie KR, Drago MD, Duffy KK, Dumas MT, Fager DC, Glod BLC, Hansen KE, Hill CR, Leising RM, Lynes CL, Macinnis AE, McGohey MR, ... ... Leadbeater NE, et al. 1,3-γ-Silyl-elimination in electron-deficient cationic systems Chemical Science. 5: 3983-3994. DOI: 10.1039/C4Sc01732C |
0.795 |
|
2014 |
Stencel LM, Leadbeater NE. Application of a new interface for rapid optimisation of bio-catalysed processes: Proteolytic digestion and an enzyme-catalysed transesterification as examples New Journal of Chemistry. 38: 242-247. DOI: 10.1039/C3Nj00784G |
0.799 |
|
2014 |
Hamlin TA, Lazarus GML, Kelly CB, Leadbeater NE. A continuous-flow approach to 3,3,3-trifluoromethylpropenes: Bringing together grignard addition, peterson elimination, inline extraction, and solvent switching Organic Process Research and Development. 18: 1253-1258. DOI: 10.1021/Op500190J |
0.709 |
|
2013 |
Kelly CB, Mercadante MA, Leadbeater NE. Trifluoromethyl ketones: properties, preparation, and application. Chemical Communications (Cambridge, England). 49: 11133-48. PMID 24162741 DOI: 10.1039/C3Cc46266H |
0.783 |
|
2013 |
Hamlin TA, Leadbeater NE. Raman spectroscopy as a tool for monitoring mesoscale continuous-flow organic synthesis: Equipment interface and assessment in four medicinally-relevant reactions. Beilstein Journal of Organic Chemistry. 9: 1843-52. PMID 24062851 DOI: 10.3762/Bjoc.9.215 |
0.645 |
|
2013 |
Kelly CB, Mercadante MA, Wiles RJ, Leadbeater NE. Oxidative esterification of aldehydes using a recyclable oxoammonium salt. Organic Letters. 15: 2222-5. PMID 23614873 DOI: 10.1021/Ol400785D |
0.806 |
|
2013 |
Mercadante MA, Kelly CB, Bobbitt JM, Tilley LJ, Leadbeater NE. Synthesis of 4-acetamido-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate and 4-acetamido-(2,2,6,6-tetramethyl-piperidin-1-yl)oxyl and their use in oxidative reactions. Nature Protocols. 8: 666-76. PMID 23471111 DOI: 10.1038/Nprot.2013.028 |
0.844 |
|
2013 |
Hamlin TA, Leadbeater NE. Raman spectroscopy as a tool for monitoring mesoscale continuous-flow organic synthesis: Equipment interface and assessment in four medicinally-relevant reactions Beilstein Journal of Organic Chemistry. 9: 1843-1852. DOI: 10.3762/bjoc.9.215 |
0.6 |
|
2013 |
Rudzinski DM, Leadbeater NE. Microwave heating and conventionallyheated continuous-flow processing as tools for performing cleaner palladium-catalyzed decarboxylative couplings using oxygen as the oxidant - A proof of principle study Green Processing and Synthesis. 2: 323-328. DOI: 10.1515/gps-2013-0043 |
0.303 |
|
2013 |
Hamlin TA, Kelly CB, Leadbeater NE. Dehydrogenation of perfluoroalkyl ketones by using a recyclable oxoammonium salt European Journal of Organic Chemistry. 3658-3661. DOI: 10.1002/Ejoc.201300392 |
0.75 |
|
2013 |
Leadbeater NE, Schmink JR, Hamlin TA. Tools for Monitoring Reactions Performed Using Microwave Heating Microwaves in Organic Synthesis: Third Edition. 1: 347-376. DOI: 10.1002/9783527651313.ch8 |
0.802 |
|
2012 |
Kelly CB, Mercadante MA, Hamlin TA, Fletcher MH, Leadbeater NE. Oxidation of α-trifluoromethyl alcohols using a recyclable oxoammonium salt. The Journal of Organic Chemistry. 77: 8131-41. PMID 22931546 DOI: 10.1021/Jo301477S |
0.824 |
|
2012 |
Rudzinski DM, Kelly CB, Leadbeater NE. A Weinreb amide approach to the synthesis of trifluoromethylketones. Chemical Communications (Cambridge, England). 48: 9610-2. PMID 22911019 DOI: 10.1039/C2Cc35037H |
0.535 |
|
2012 |
Eddy NA, Kelly CB, Mercadante MA, Leadbeater NE, Fenteany G. Access to dienophilic ene-triketone synthons by oxidation of diketones with an oxoammonium salt. Organic Letters. 14: 498-501. PMID 22206582 DOI: 10.1021/Ol2030873 |
0.837 |
|
2012 |
Mercadante MA, Leadbeater NE. Development of methodologies for reactions involving gases as reagents: Microwave heating and conventionally-heated continuous-flow processing as examples Green Processing and Synthesis. 1: 499-507. DOI: 10.1515/Gps-2011-0016 |
0.777 |
|
2012 |
Mercadante MA, Kelly CB, Lee C, Leadbeater NE. Continuous flow hydrogenation using an on-demand gas delivery reactor Organic Process Research and Development. 16: 1064-1068. DOI: 10.1021/Op300019W |
0.783 |
|
2011 |
Mercadante MA, Leadbeater NE. Continuous-flow, palladium-catalysed alkoxycarbonylation reactions using a prototype reactor in which it is possible to load gas and heat simultaneously Organic and Biomolecular Chemistry. 9: 6575-6578. PMID 21850299 DOI: 10.1039/C1Ob05808H |
0.783 |
|
2011 |
Kelly CB, Lee C, Mercadante MA, Leadbeater NE. A continuous-flow approach to palladium-catalyzed alkoxycarbonylation reactions Organic Process Research and Development. 15: 717-720. DOI: 10.1021/Op200037N |
0.808 |
|
2011 |
Kelly CB, Lee CX, Leadbeater NE. Copper-catalyzed direct preparation of diaryl sulfides from aryl iodides using potassium thiocyanate as a sulfur transfer reagent Tetrahedron Letters. 52: 4587-4589. DOI: 10.1016/J.Tetlet.2011.06.107 |
0.586 |
|
2011 |
Kelly CB, Lee C, Leadbeater NE. An approach for continuous-flow processing of reactions that involve the in situ formation of organic products Tetrahedron Letters. 52: 263-265. DOI: 10.1016/J.Tetlet.2010.11.027 |
0.56 |
|
2010 |
Leadbeater NE. In situ reaction monitoring of microwave-mediated reactions using IR spectroscopy. Chemical Communications (Cambridge, England). 46: 6693-5. PMID 20717594 DOI: 10.1039/c0cc01921f |
0.333 |
|
2010 |
Leadbeater NE. In situ reaction monitoring of microwave-mediated reactions using IR spectroscopy Chemical Communications. 46: 6693-6695. DOI: 10.1039/c0cc01921f |
0.333 |
|
2010 |
Leadbeater NE. In situ reaction monitoring of microwave-mediated reactions using IR spectroscopy Chemical Communications. 46: 6693-6695. DOI: 10.1039/c0cc01921f |
0.333 |
|
2010 |
Schmink JR, Kormos CM, Devine WG, Leadbeater NE. Exploring the scope for scale-up of organic chemistry using a large batch microwave reactor Organic Process Research and Development. 14: 205-214. DOI: 10.1021/Op900287J |
0.802 |
|
2009 |
Schmink JR, Leadbeater NE. Probing "microwave effects" using Raman spectroscopy. Organic & Biomolecular Chemistry. 7: 3842-6. PMID 19707691 DOI: 10.1039/B910591C |
0.673 |
|
2009 |
Stencel LM, Kormos CM, Avery KB, Leadbeater NE. Assessment and use of two silicon carbide multi-well plates for library synthesis and proteolytic digests using microwave heating Organic and Biomolecular Chemistry. 7: 2452-2457. PMID 19462057 DOI: 10.1039/B902112D |
0.792 |
|
2009 |
Schmink JR, Leadbeater NE. Palladium-catalyzed synthesis of diarylmethanes: exploitation of carbanionic leaving groups. Organic Letters. 11: 2575-8. PMID 19456122 DOI: 10.1021/Ol900874Z |
0.727 |
|
2009 |
Schmink JR, Holcomb JL, Leadbeater NE. Testing the validity of microwave-interfaced, in situ Raman spectroscopy as a tool for kinetic studies. Organic Letters. 11: 365-8. PMID 19072323 DOI: 10.1021/Ol802594S |
0.748 |
|
2009 |
Kormos CM, Hull RM, Leadbeater NE. Microwave heating in conjunction with UV irradiation: A tool for the oxidation of 1,4-dihydropyridines to pyridines Australian Journal of Chemistry. 62: 51-57. DOI: 10.1071/Ch08414 |
0.76 |
|
2009 |
Kormos CM, Hull RM, Leadbeater NE. Microwave heating in conjunction with UV irradiation: A tool for the oxidation of 1,4-dihydropyridines to pyridines Australian Journal of Chemistry. 62: 51-57. DOI: 10.1071/CH08414 |
0.302 |
|
2009 |
Schmink JR, Leadbeater NE. Probing "microwave effects" using Raman spectroscopy Organic and Biomolecular Chemistry. 7: 3842-3846. DOI: 10.1039/b910591c |
0.669 |
|
2009 |
Iannelli M, Bergamelli F, Kormos CM, Paravisi S, Leadbeater NE. Application of a batch microwave unit for scale-up of alkoxycarbonylation reactions using a near-stoichiometric loading of carbon monoxide Organic Process Research and Development. 13: 634-637. DOI: 10.1021/Op800296D |
0.714 |
|
2009 |
Schmink JR, Leadbeater NE. Palladium-catalyzed synthesis of diarylmethanes: Exploitation of carbanionic leaving groups Organic Letters. 11: 2575-2578. DOI: 10.1021/ol900874z |
0.722 |
|
2009 |
Schmink JR, Holcomb JL, Leadbeater NE. Testing the validity of microwave-interfaced, in situ Raman spectroscopy as a tool for kinetic studies Organic Letters. 11: 365-368. DOI: 10.1021/ol802594s |
0.681 |
|
2009 |
Avery KB, Devine WG, Kormos CM, Leadbeater NE. Use of a silicon carbide multi-well plate in conjunction with microwave heating for rapid ligand synthesis, formation of palladium complexes, and catalyst screening in a Suzuki coupling Tetrahedron Letters. 50: 2851-2853. DOI: 10.1016/J.Tetlet.2009.03.140 |
0.723 |
|
2009 |
Leadbeater NE, Kormos CM. ChemInform Abstract: Microwave Heating as a Safe, Versatile Tool for Reactions Involving Gaseous Reagents Cheminform. 40. DOI: 10.1002/chin.200929241 |
0.746 |
|
2009 |
Kormos CM, Hull RM, Leadbeater NE. ChemInform Abstract: Microwave Heating in Conjunction with UV Irradiation: A Tool for the Oxidation of 1,4-Dihydropyridines to Pyridines. Cheminform. 40. DOI: 10.1002/CHIN.200927137 |
0.308 |
|
2008 |
Schmink JR, Holcomb JL, Leadbeater NE. Use of Raman spectroscopy as an in situ tool to obtain kinetic data for organic transformations. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 9943-50. PMID 18830985 DOI: 10.1002/Chem.200801158 |
0.762 |
|
2008 |
Kormos CM, Leadbeater NE. Preparation of nonsymmetrically substituted stilbenes in a one-pot two-step Heck strategy using ethene as a reagent Journal of Organic Chemistry. 73: 3854-3858. PMID 18410149 DOI: 10.1021/Jo800235C |
0.732 |
|
2008 |
Dean ML, Schmink JR, Leadbeater NE, Brückner C. Microwave-promoted insertion of Group 10 metals into free base porphyrins and chlorins: scope and limitations. Dalton Transactions (Cambridge, England : 2003). 1341-5. PMID 18305846 DOI: 10.1039/B716181F |
0.723 |
|
2008 |
Leadbeater NE, Schmink JR. Use of Raman spectroscopy as a tool for in situ monitoring of microwave-promoted reactions Nature Protocols. 3: 1-7. PMID 18193016 DOI: 10.1038/Nprot.2007.453 |
0.763 |
|
2008 |
Dean ML, Schmink JR, Leadbeater NE, Brückner C. Microwave-promoted insertion of Group 10 metals into free base porphyrins and chlorins: Scope and limitations Dalton Transactions. 1341-1345. DOI: 10.1039/b716181f |
0.689 |
|
2008 |
Bowman MD, Schmink JR, McGowan CM, Kormos CM, Leadbeater NE. Scale-up of microwave-promoted reactions to the multigram level using a sealed-vessel microwave apparatus Organic Process Research and Development. 12: 1078-1088. DOI: 10.1021/Op8001239 |
0.818 |
|
2008 |
Bowman MD, Holcomb JL, Kormos CM, Leadbeater NE, Williams VA. Approaches for scale-up of microwave-promoted reactions Organic Process Research and Development. 12: 41-57. DOI: 10.1021/Op700187W |
0.741 |
|
2008 |
Leadbeater NE, Barnard TM, Stencel LM. Batch and continuous-flow preparation of biodiesel derived from butanol and facilitated by microwave heating Energy and Fuels. 22: 2005-2008. DOI: 10.1021/Ef700748T |
0.795 |
|
2008 |
Schmink JR, Holcomb JL, Leadbeater NE. Use of Raman spectroscopy as an in situ tool to obtain kinetic data for organic transformations Chemistry - a European Journal. 14: 9943-9950. DOI: 10.1002/chem.200801158 |
0.683 |
|
2008 |
Kormos CM, Leadbeater NE. Palladium-catalyzed reactions with gaseous reagents: Carbonylation with carbon monoxide, Heck reaction with ethene Acs National Meeting Book of Abstracts. |
0.744 |
|
2008 |
Kormos CM, Leadbeater NE. Palladium-catalyzed reactions with gaseous reagents: Carbonylation with carbon monoxide, Heck reaction with ethene Acs National Meeting Book of Abstracts. |
0.337 |
|
2008 |
Stencel LM, Barnard TM, Leadbeater NE. Microwave heating for fast, easy biodiesel preparation Acs National Meeting Book of Abstracts. |
0.784 |
|
2008 |
Leadbeater NE, Stencel LM. Microwave heating as a versatile tool for preparing biodiesel Acs National Meeting Book of Abstracts. |
0.784 |
|
2007 |
Leadbeater NE, Stencel LM, Wood EC. Probing the effects of microwave irradiation on enzyme-catalysed organic transformations: The case of lipase-catalysed transesterification reactions Organic and Biomolecular Chemistry. 5: 1052-1055. PMID 17377658 DOI: 10.1039/B617544A |
0.825 |
|
2007 |
Leadbeater NE, Smith RJ, Barnard TM. Using in situ Raman monitoring as a tool for rapid optimisation and scale-up of microwave-promoted organic synthesis: esterification as an example. Organic & Biomolecular Chemistry. 5: 822-5. PMID 17315069 DOI: 10.1039/b615597a |
0.321 |
|
2007 |
Kormos CM, Leadbeater NE. Alkoxycarbonylation of aryl iodides using gaseous carbon monoxide and pre-pressurized reaction vessels in conjunction with microwave heating. Organic & Biomolecular Chemistry. 5: 65-8. PMID 17164908 DOI: 10.1039/B614025D |
0.754 |
|
2007 |
Kormos CM, Leadbeater NE. Alkoxycarbonylation reactions performed using near-stoichiometric quantities of CO Synlett. 2006-2010. DOI: 10.1055/S-2007-984883 |
0.739 |
|
2007 |
Kormos CM, Leadbeater NE. Alkoxycarbonylation reactions performed using near-stoichiometric quantities of CO Synlett. 2006-2010. DOI: 10.1055/s-2007-984883 |
0.319 |
|
2007 |
Kormos CM, Leadbeater NE. Alkoxycarbonylation of aryl iodides using gaseous carbon monoxide and pre-pressurized reaction vessels in conjunction with microwave heating Organic and Biomolecular Chemistry. 5: 65-68. DOI: 10.1039/b614025d |
0.719 |
|
2007 |
Barnard TM, Leadbeater NE, Boucher MB, Stencel LM, Wilhite BA. Continuous-flow preparation of biodiesel using microwave heating Energy and Fuels. 21: 1777-1781. DOI: 10.1021/Ef0606207 |
0.806 |
|
2007 |
Leadbeater NE, Schmink JR. Use of a scientific microwave apparatus for rapid optimization of reaction conditions in a monomode function and then substrate screening in a multimode function Tetrahedron. 63: 6764-6773. DOI: 10.1016/J.Tet.2007.04.074 |
0.749 |
|
2006 |
Leadbeater NE, Smith RJ. Real-time monitoring of microwave-promoted Suzuki coupling reactions using in situ Raman spectroscopy. Organic Letters. 8: 4589-91. PMID 16986957 DOI: 10.1021/ol061803f |
0.325 |
|
2006 |
Kormos CM, Leadbeater NE. Microwave-promoted hydroxycarbonylation in water using gaseous carbon monoxide and pre-pressurized reaction vessels Synlett. 1663-1666. DOI: 10.1055/S-2006-944216 |
0.729 |
|
2006 |
Leadbeater NE, Stencel LM. Fast, easy preparation of biodiesel using microwave heating Energy and Fuels. 20: 2281-2283. DOI: 10.1021/Ef060163U |
0.788 |
|
2006 |
Amore KM, Leadbeater NE, Miller TA, Schmink JR. Fast, easy, solvent-free, microwave-promoted Michael addition of anilines to α,β-unsaturated alkenes: synthesis of N-aryl functionalized β-amino esters and acids Tetrahedron Letters. 47: 8583-8586. DOI: 10.1016/J.Tetlet.2006.09.114 |
0.726 |
|
2006 |
Arvela RK, Leadbeater NE, Mack TL, Kormos CM. Microwave-promoted Suzuki coupling reactions with organotrifluoroborates in water using ultra-low catalyst loadings Tetrahedron Letters. 47: 217-220. DOI: 10.1016/J.Tetlet.2005.10.153 |
0.719 |
|
2006 |
Kormos CM, Leadbeater NE. Direct conversion of aryl halides to phenols using high-temperature or near-critical water and microwave heating Tetrahedron. 62: 4728-4732. DOI: 10.1016/J.Tet.2006.01.103 |
0.7 |
|
2005 |
Arvela RK, Leadbeater NE. Suzuki coupling of aryl chlorides with phenylboronic acid in water, using microwave heating with simultaneous cooling. Organic Letters. 7: 2101-4. PMID 15901144 DOI: 10.1021/ol0503384 |
0.308 |
|
2003 |
Leadbeater NE, Torenius HM, Tye H. Microwave-assisted Mannich-type three-component reactions Molecular Diversity. 7: 135-144. PMID 14870842 DOI: 10.1023/B:MODI.0000006822.51884.e6 |
0.336 |
|
2003 |
Arvela RK, Leadbeater NE. Rapid, easy cyanation of aryl bromides and chlorides using nickel salts in conjunction with microwave promotion. The Journal of Organic Chemistry. 68: 9122-5. PMID 14604393 DOI: 10.1021/jo0350561 |
0.383 |
|
2003 |
Leadbeater NE, Marco M. Transition-metal-free Suzuki-type coupling reactions: scope and limitations of the methodology. The Journal of Organic Chemistry. 68: 5660-7. PMID 12839459 DOI: 10.1021/jo034230i |
0.353 |
|
2003 |
Leadbeater NE, Marco M. Rapid and amenable suzuki coupling reaction in water using microwave and conventional heating. The Journal of Organic Chemistry. 68: 888-92. PMID 12558412 DOI: 10.1021/jo0264022 |
0.36 |
|
2002 |
Leadbeater NE, Marco M. Ligand-free palladium catalysis of the Suzuki reaction in water using microwave heating. Organic Letters. 4: 2973-6. PMID 12182602 DOI: 10.1021/ol0263907 |
0.347 |
|
2002 |
Lattanzi A, Leadbeater NE. Microencapsulated VO(acac)2: preparation and use in allylic alcohol epoxidation. Organic Letters. 4: 1519-21. PMID 11975618 DOI: 10.1021/ol0257474 |
0.348 |
|
2002 |
Grainger RS, Leadbeater NE, Masdéu Pàmies A. The tetramethylguanidine catalyzed Baylis-Hillman reaction: Effects of co-catalysts and alcohol solvents on reaction rate Catalysis Communications. 3: 449-452. DOI: 10.1016/S1566-7367(02)00178-4 |
0.328 |
|
1999 |
Leadbeater N. Enlightening organometallic chemistry: The photochemistry of Fe(CO)5 and the reaction chemistry of unsaturated iron carbonyl fragments Coordination Chemistry Reviews. 188: 35-70. DOI: 10.1016/S0010-8545(98)00217-3 |
0.348 |
|
1998 |
Hay CM, Leadbeater NE, Lewis J, Raithby PR, Burgess K. Photochemistry of Os3(CO)12 with AuPPh3Cl: synthesis and structural characterisation of (μ-AuPPh3)(μ-Cl)Os3(CO)10 New Journal of Chemistry. 22: 787-788. DOI: 10.1039/A802946F |
0.49 |
|
1995 |
Edwards AJ, Leadbeater NE, Lewis J, Raithby PR. Reaction chemistry of alkynes with the tris(acetonitrile)-ruthenium cluster [Ru3(CO)9(MeCN)3] Journal of the Chemical Society, Dalton Transactions. 3785-3787. DOI: 10.1039/Dt9950003785 |
0.399 |
|
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