| Year |
Citation |
Score |
| 2020 |
Chung EM-B, Stones MK, Latifi E, Moore C, Sutton AD, Umphrey G, Soldatov D, Schlaf M. Ruthenium triphos complexes [Ru(X(CH2PPh2)3-κ3-P)(NCCH3)3](OTf)2; X = H3C-C, N) as catalysts for the conversion of furfuryl acetate to 1,4-pentanediol and cyclopentanol in aqueous medium Canadian Journal of Chemistry. 1-14. DOI: 10.1139/Cjc-2019-0374 |
0.627 |
|
| 2020 |
Stones MK, Banz Chung EM, da Cunha IT, Sullivan RJ, Soltanipanah P, Magee M, Umphrey GJ, Moore CM, Sutton AD, Schlaf M. Conversion of Furfural Derivatives to 1,4-Pentanediol and Cyclopentanol in Aqueous Medium Catalyzed by trans-[(2,9-Dipyridyl-1,10-phenanthroline)(CH3CN)2Ru](OTf)2 Acs Catalysis. 10: 2667-2683. DOI: 10.1021/Acscatal.9B05055 |
0.702 |
|
| 2020 |
Stones MK, Sullivan RJ, Soldatov DV, Schlaf M. Synthesis and characterization of novel tetradentate ruthenium complexes of a pyridine-o-phenylenediamine based chelate ligand Inorganica Chimica Acta. 502: 119391. DOI: 10.1016/J.Ica.2019.119391 |
0.354 |
|
| 2017 |
Latifi E, Marchese AD, Hulls MCW, Soldatov DV, Schlaf M. [Ru(triphos)(CH3CN)3](OTf)2 as a homogeneous catalyst for the hydrogenation of biomass derived 2,5-hexanedione and 2,5-dimethyl-furan in aqueous acidic medium Green Chemistry. 19: 4666-4679. DOI: 10.1039/C7Gc01956D |
0.461 |
|
| 2016 |
Sullivan RJ, Kim J, Hoyt C, Silks LA, Schlaf M. Ruthenium-8-quinolinethiolate-phenylterpyridine versus ruthenium-bipyridine-phenyl-terpyridine complexes as homogeneous water and high temperature stable hydrogenation catalysts for biomass-derived substrates Polyhedron. 108: 104-114. DOI: 10.1016/J.Poly.2015.10.049 |
0.474 |
|
| 2015 |
Minard TA, Oswin CT, Waldie FDC, Howell JK, Scott BMT, Mondo DD, Sullivan RJ, Stein B, Jennings M, Schlaf M. In situ generation of water-stable and -soluble ruthenium complexes of pyridine-based chelate-ligands and their use for the hydrodeoxygenation of biomass-related substrates in aqueous acidic medium Journal of Molecular Catalysis a: Chemical. DOI: 10.1016/J.Molcata.2015.08.026 |
0.504 |
|
| 2014 |
Cristina de Resende E, Carvalho IdRG, Schlaf M, Guerreiro MC. Red Mud waste from the Bayer process as a catalyst for the desulfurization of hydrocarbon fuels Rsc Adv.. 4: 47287-47296. DOI: 10.1039/C4Ra07635D |
0.327 |
|
| 2014 |
Sullivan RJ, Latifi E, Chung BK-, Soldatov DV, Schlaf M. Hydrodeoxygenation of 2,5-Hexanedione and 2,5-Dimethylfuran by Water-, Air-, and Acid-Stable Homogeneous Ruthenium and Iridium Catalysts Acs Catalysis. 4: 4116-4128. DOI: 10.1021/Cs501202T |
0.473 |
|
| 2014 |
Karimi E, Teixeira IF, Gomez A, de Resende E, Gissane C, Leitch J, Jollet V, Aigner I, Berruti F, Briens C, Fransham P, Hoff B, Schrier N, Lago RM, Kycia SW, ... ... Schlaf M, et al. Synergistic co-processing of an acidic hardwood derived pyrolysis bio-oil with alkaline Red Mud bauxite mining waste as a sacrificial upgrading catalyst Applied Catalysis B: Environmental. 145: 187-196. DOI: 10.1016/J.Apcatb.2013.02.007 |
0.333 |
|
| 2013 |
Sutton AD, Waldie FD, Wu R, Schlaf M, Silks LA, Gordon JC. The hydrodeoxygenation of bioderived furans into alkanes. Nature Chemistry. 5: 428-32. PMID 23609095 DOI: 10.1038/Nchem.1609 |
0.647 |
|
| 2013 |
Resende ECD, Gissane C, Nicol R, Heck RJ, Guerreiro MC, Coelho JV, Oliveira LCAD, Palmisano P, Berruti F, Briens C, Schlaf M. Synergistic co-processing of Red Mud waste from the Bayer process and a crude untreated waste stream from bio-diesel production Green Chemistry. 15: 496-510. DOI: 10.1039/C2Gc36714A |
0.388 |
|
| 2013 |
Sutton AD, Waldie FD, Wu R, Schlaf M, 'Pete' Silks LA, Gordon JC. Erratum: The hydrodeoxygenation of bioderived furans into alkanes Nature Chemistry. 5: 544-544. DOI: 10.1038/Nchem.1664 |
0.605 |
|
| 2013 |
DiMondo D, Thibault ME, Britten J, Schlaf M. Comparison of the Catalytic Activity of [(η5-C5H5)Ru(2,2′-bipyridine)(L)]OTf versus [(η5-C5H5)Ru(6,6′-diamino-2,2′-bipyridine)(L)]OTf (L = labile ligand) in the Hydrogenation of Cyclohexanone. Evidence for the Presence of a Metal–Ligand Bifunctional Mechanism under Acidic Conditions Organometallics. 32: 6541-6554. DOI: 10.1021/Om400871V |
0.401 |
|
| 2012 |
Acosta-Ramirez A, Bertoli M, Gusev DG, Schlaf M. Homogeneous catalytic hydrogenation of long-chain esters by an osmium pincer complex and its potential application in the direct conversion of triglycerides into fatty alcohols Green Chemistry. 14: 1178-1188. DOI: 10.1039/C2Gc15960K |
0.421 |
|
| 2012 |
Karimi E, Teixeira IF, Ribeiro LP, Gomez A, Lago RM, Penner G, Kycia SW, Schlaf M. Ketonization and deoxygenation of alkanoic acids and conversion of levulinic acid to hydrocarbons using a Red Mud bauxite mining waste as the catalyst Catalysis Today. 190: 73-88. DOI: 10.1016/J.Cattod.2011.11.028 |
0.47 |
|
| 2011 |
Thibault ME, DiMondo DV, Jennings M, Abdelnur PV, Eberlin MN, Schlaf M. Cyclopentadienyl and pentamethylcyclopentadienyl ruthenium complexes as catalysts for the total deoxygenation of 1,2-hexanediol and glycerol Green Chemistry. 13: 357-366. DOI: 10.1039/C0Gc00255K |
0.481 |
|
| 2011 |
Di Mondo D, Ashok D, Waldie F, Schrier N, Morrison M, Schlaf M. Stainless Steel As a Catalyst for the Total Deoxygenation of Glycerol and Levulinic Acid in Aqueous Acidic Medium Acs Catalysis. 1: 355-364. DOI: 10.1021/Cs200053H |
0.4 |
|
| 2010 |
Karimi E, Briens C, Berruti F, Moloodi S, Tzanetakis T, Thomson MJ, Schlaf M. Red mud as a catalyst for the upgrading of hemp-seed pyrolysis bio-oil Energy and Fuels. 24: 6586-6600. DOI: 10.1021/Ef101154D |
0.333 |
|
| 2010 |
Karimi E, Gomez A, Kycia SW, Schlaf M. Thermal Decomposition of Acetic and Formic Acid Catalyzed by Red Mud—Implications for the Potential Use of Red Mud as a Pyrolysis Bio-Oil Upgrading Catalyst§§ Dedicated to Prof. Ulf Schuchardt on the occasion of his retirement. Energy & Fuels. 24: 2747-2757. DOI: 10.1021/Ef1000375 |
0.367 |
|
| 2009 |
Taher D, Thibault ME, Di Mondo D, Jennings M, Schlaf M. Acid-, water- and high-temperature-stable ruthenium complexes for the total catalytic deoxygenation of glycerol to propane. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 10132-43. PMID 19693757 DOI: 10.1002/Chem.200901427 |
0.464 |
|
| 2009 |
Schlaf M, Thibault ME, DiMondo D, Taher D, Karimi E, Ashok D. Bioenergy II: Group 8 Metal Complexes as Homogeneous Ionic Hydrogenation and Hydrogenolysis Catalysts for the Deoxygenation of Biomass to Petrochemicals - Opportunities, Challenges, Strategies and the Story so Far International Journal of Chemical Reactor Engineering. 7. DOI: 10.2202/1542-6580.1905 |
0.433 |
|
| 2009 |
Schlaf M, Ghosh P, Fagan P, Hauptman E, Bullock RM. Catalytic Deoxygenation of 1,2-Propanediol to Given-Propanol Advanced Synthesis & Catalysis. 351: 789-800. DOI: 10.1002/Adsc.200800685 |
0.437 |
|
| 2008 |
Bosch M, Handerson S, Schlaf M. Optimized Synthesis of Vinyl Ether Sugars and Vinyl Glycosides through Transfer Vinylation Catalyzed by (4,7‐Ph2‐phen)Pd(OOCCF3)2 Journal of Carbohydrate Chemistry. 27: 103-112. DOI: 10.1080/07328300802030852 |
0.708 |
|
| 2008 |
Youm JJY, Schlaf M, Bierenstiel M. Acceleration of bromide mediated benzoylperoxide oxidations of secondary alcohols in aqueous organic solvents Tetrahedron Letters. 49: 3199-3203. DOI: 10.1016/J.Tetlet.2008.03.098 |
0.32 |
|
| 2008 |
Bierenstiel M, Dymarska M, Jong Ed, Schlaf M. An evaluation of the Noyori system in reverse : Thermodynamic and kinetic parameters of secondary alcohol transfer dehydrogenation catalyzed by [(η6-1-iPr-4-Me-C6H4)Ru(HN-CR'R -CR'R NTs)], R'=H, Me; Ph, R =H, Me Journal of Molecular Catalysis a-Chemical. 290: 1-14. DOI: 10.1016/J.Molcata.2008.05.009 |
0.504 |
|
| 2007 |
Thibault ME, Luska KL, Schlaf M. An Improved Synthesis of 6,6′-Diamino-2,2′-bipyridine Synthesis. 2007: 791-793. DOI: 10.1055/S-2007-965905 |
0.412 |
|
| 2007 |
Dykeman RR, Luska KL, Thibault ME, Jones MD, Schlaf M, Khanfar M, Taylor NJ, Britten JF, Harrington L. Catalytic deoxygenation of terminal-diols under acidic aqueous conditions by the ruthenium complexes [(η6-arene)Ru(X)(N ∩ N)](OTf)n, X = H2O, H, η6-arene =.. Journal of Molecular Catalysis a: Chemical. 277: 233-251. DOI: 10.1016/J.Molcata.2007.08.008 |
0.39 |
|
| 2006 |
Schlaf M. Selective deoxygenation of sugar polyols to alpha,omega-diols and other oxygen content reduced materials--a new challenge to homogeneous ionic hydrogenation and hydrogenolysis catalysis. Dalton Transactions (Cambridge, England : 2003). 4645-53. PMID 17028671 DOI: 10.1039/B608007C |
0.355 |
|
| 2005 |
Chung MK, Schlaf M. Regioselectively trisilylated hexopyranosides through homogeneously catalyzed silane alcoholysis. Journal of the American Chemical Society. 127: 18085-92. PMID 16366560 DOI: 10.1021/Ja056283I |
0.78 |
|
| 2005 |
Bierenstiel M, D'Hondt PJ, Schlaf M. Investigations into the selective oxidation of vicinal diols to α-hydroxy ketones with the NaBrO3/NaHSO3 reagent: pH dependence, stoichiometry, substrates and origin of selectivity Tetrahedron. 61: 4911-4917. DOI: 10.1016/J.Tet.2005.03.056 |
0.334 |
|
| 2005 |
Xie Z, Schlaf M. Direct transformation of terminal vic-diols to primary alcohols and alkanes through hydrogenation catalyzed by [cis-Ru(6,6′-Cl2-bipy)2(OH2)2](CF3SO3)2 in acidic medium Journal of Molecular Catalysis a: Chemical. 229: 151-158. DOI: 10.1016/J.Molcata.2004.11.018 |
0.477 |
|
| 2004 |
Chung MK, Schlaf M. A catalytic synthesis of thiosilanes and silthianes: palladium nanoparticle-mediated cross-coupling of silanes with thio phenyl and thio vinyl ethers through selective carbon-sulfur bond activation. Journal of the American Chemical Society. 126: 7386-92. PMID 15186178 DOI: 10.1021/Ja049386U |
0.769 |
|
| 2004 |
Bierenstiel M, Schlaf M. δ‐Galactonolactone: Synthesis, Isolation, and Comparative Structure and Stability Analysis of an Elusive Sugar Derivative European Journal of Organic Chemistry. 2004: 1474-1481. DOI: 10.1002/Ejoc.200300761 |
0.304 |
|
| 2003 |
Bosch M, Schlaf M. Synthesis of allyl and alkyl vinyl ethers using an in situ prepared air-stable palladium catalyst. Efficient transfer vinylation of primary, secondary, and tertiary alcohols. The Journal of Organic Chemistry. 68: 5225-7. PMID 12816481 DOI: 10.1021/Jo034376H |
0.711 |
|
| 2002 |
Chung MK, Orlova G, Goddard JD, Schlaf M, Harris R, Beveridge TJ, White G, Hallett FR. Regioselective silylation of sugars through palladium nanoparticle-catalyzed silane alcoholysis. Journal of the American Chemical Society. 124: 10508-18. PMID 12197753 DOI: 10.1021/Ja026723V |
0.768 |
|
| 2002 |
Handerson S, Schlaf M. Palladium(II)-catalyzed transfer vinylation of protected monosaccharides. Organic Letters. 4: 407-9. PMID 11820891 DOI: 10.1021/Ol017104E |
0.542 |
|
| 2002 |
Chung MK, Orlova G, Goddard JD, Schlaf M, Harris R, Beveridge TJ, White G, Hallett FR. Regioselective silylation of sugars through palladium nanoparticle-catalyzed silane alcoholysis Journal of the American Chemical Society. 124: 10508-10518. DOI: 10.1021/ja026723v |
0.718 |
|
| 2001 |
Schlaf M, Ghosh P, Fagan PJ, Hauptman E, Bullock RM. Metal-Catalyzed Selective Deoxygenation of Diols to Alcohols. Angewandte Chemie (International Ed. in English). 40: 3887-3890. PMID 29712139 DOI: 10.1002/1521-3773(20011015)40:20<3887::Aid-Anie3887>3.0.Co;2-Q |
0.382 |
|
| 2001 |
Chung M, Ferguson G, Robertson V, Schlaf M. Nature of the active silane alcoholysis catalyst in the RuwClx(CO)y(PMe3)z (w, x, y, z = 1 or 2) system; Ru2(µ-Cl)2Cl2(CO)4(PMe3)2 as a new catalyst for silane alcoholysis in a polar solvent Canadian Journal of Chemistry. 79: 949-957. DOI: 10.1139/V00-193 |
0.762 |
|
| 1997 |
Schlaf M, Lough AJ, Morris RH. Synthesis and Structure of the Chiral Dihydrogen Complextrans-[Ru(η2-H2)H(R,R‘-Me-DuPHOS)2]PF6and the Dinitrogen Complextrans-[Ru(N2)H(R,R‘-Me-DuPHOS)2]PF6(R,R‘-Me-DuPHOS = 1,2-Bis((2R,5R)-2,5-dimethylphospholano)benzene) Organometallics. 16: 1253-1259. DOI: 10.1021/Om960410P |
0.311 |
|
| 1996 |
Schlaf M, Lough AJ, Morris RH. Dihydrogen Thiolate vs Hydride Thiol: Reactivity of the Series of Complexes MH(CO)(L)(PPh3)2(M = Ru, Os; L = Pyridine-2-thiolate, Quinoline-8-thiolate) with Acid. X-ray Structure Determination of [Os(CO)(μ2-Spy)(SpyH)(PPh3)]2[BF4]2 Organometallics. 15: 4423-4436. DOI: 10.1021/Om960411H |
0.304 |
|
| 1996 |
Schlaf M, Lough AJ, Maltby PA, Morris RH. Synthesis, Structure, and Properties of the Stable and Highly Acidic Dihydrogen Complextrans-[Os(η2-H2)(CH3CN)(dppe)2](BF4)2. Perspectives on the Influence of thetransLigand on the Chemistry of the Dihydrogen Ligand Organometallics. 15: 2270-2278. DOI: 10.1021/Om960113K |
0.319 |
|
| 1996 |
Maltby PA, Schlaf M, Steinbeck M, Lough AJ, Morris RH, Klooster WT, Koetzle TF, Srivastava RC. Dihydrogen with Frequency of Motion Near the1H Larmor Frequency. Solid-State Structures and Solution NMR Spectroscopy of Osmium Complexestrans-[Os(H··H)X(PPh2CH2CH2PPh2)2]+(X = Cl, Br) Journal of the American Chemical Society. 118: 5396-5407. DOI: 10.1021/Ja9529044 |
0.307 |
|
| 1995 |
Schlaf M, Morris RH. A dihydrogen complex, [Os(η2-H2)(CO)(quS)(PPh3)2]+, in equilibrium with its coordinated thiol tautomer (quS = quinoline-8-thiolate) Journal of the Chemical Society, Chemical Communications. 625-626. DOI: 10.1039/C39950000625 |
0.3 |
|
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