| Year |
Citation |
Score |
| 2021 |
Kozack CV, Tereniak SJ, Jaworski JN, Li B, Bruns DL, Knapp SMM, Landis CR, Stahl SS. Benzoquinone Cocatalyst Contributions to DAF/Pd(OAc)-Catalyzed Aerobic Allylic Acetoxylation in the Absence and Presence of a Co(salophen) Cocatalyst. Acs Catalysis. 11: 6363-6370. PMID 34422447 DOI: 10.1021/acscatal.1c01074 |
0.493 |
|
| 2020 |
Cueny ES, Sita LR, Landis CR. Quantitative Validation of the Living CoordinativeChain-Transfer Polymerization of 1‑Hexene Using ChromophoreQuench Labeling Macromolecules. 53: 5816-5825. DOI: 10.1021/Acs.Macromol.0C00552 |
0.352 |
|
| 2019 |
Wright AM, Pahls DR, Gary JB, Warner T, Williams JZ, M Knapp SM, Allen KE, Landis CR, Cundari TR, Goldberg KI. Experimental and Computational Investigation of the Aerobic Oxidation of a Late Transition Metal-Hydride. Journal of the American Chemical Society. PMID 31259542 DOI: 10.1021/Jacs.9B04706 |
0.608 |
|
| 2019 |
Jaworski JN, Kozack CV, Tereniak SJ, Knapp SMM, Landis CR, Miller JT, Stahl SS. Operando Spectroscopic and Kinetic Characterization of Aerobic Allylic C-H Acetoxylation Catalyzed by Pd(OAc)2/4,5-Diazafluoren-9-one. Journal of the American Chemical Society. PMID 31184479 DOI: 10.1021/Jacs.9B04699 |
0.678 |
|
| 2019 |
Cueny ES, Landis CR. The Hafnium-Pyridyl Amido-Catalyzed Copolymerization of Ethene and 1-Octene: How Small Amounts of Ethene Impact Catalysis Acs Catalysis. 9: 3338-3348. DOI: 10.1021/Acscatal.9B00250 |
0.436 |
|
| 2019 |
Brezny AC, Landis CR. Development of a Comprehensive Microkinetic Model for Rh(bis(diazaphospholane))-Catalyzed Hydroformylation Acs Catalysis. 9: 2501-2513. DOI: 10.1021/Acscatal.9B00173 |
0.795 |
|
| 2019 |
Cueny ES, Landis CR. Zinc-Mediated Chain Transfer from Hafnium to Aluminum in the Hafnium-Pyridyl Amido-Catalyzed Polymerization of 1-Octene Revealed by Job Plot Analysis Organometallics. 38: 926-932. DOI: 10.1021/Acs.Organomet.8B00900 |
0.315 |
|
| 2018 |
Brezny AC, Landis CR. Recent Developments in the Scope, Practicality, and Mechanistic Understanding of Enantioselective Hydroformylation. Accounts of Chemical Research. PMID 30118203 DOI: 10.1021/Acs.Accounts.8B00335 |
0.836 |
|
| 2018 |
Eshon J, Foarta F, Landis CR, Schomaker JM. α-Tetrasubstituted aldehydes through electronic and strain-controlled branch-selective stereoselective hydroformylation. The Journal of Organic Chemistry. PMID 30070109 DOI: 10.3389/Conf.Fchem.2018.01.00023 |
0.489 |
|
| 2018 |
Goldman AS, Landis CR, Sen A. Jack Halpern (1925-2018). Angewandte Chemie (International Ed. in English). PMID 29570933 DOI: 10.1002/Anie.201802390 |
0.664 |
|
| 2018 |
Schmid MH, Das AK, Landis CR, Meuwly M. Multi-State VALBOND for Atomistic Simulations of Hypervalent Molecules, Metal Complexes and Reactions. Journal of Chemical Theory and Computation. PMID 29490133 DOI: 10.1021/Acs.Jctc.7B01210 |
0.301 |
|
| 2018 |
Cueny ES, Johnson HC, Landis CR. Selective Quench-Labeling of the Hafnium-Pyridyl Amido-Catalyzed Polymerization of 1-Octene in the Presence of Trialkyl-Aluminum Chain-Transfer Reagents Acs Catalysis. 8: 11605-11614. DOI: 10.1021/Acscatal.8B03615 |
0.378 |
|
| 2018 |
Johnson HC, Cueny ES, Landis CR. Chain Transfer with Dialkyl Zinc During Hafnium–Pyridyl Amido-Catalyzed Polymerization of 1-Octene: Relative Rates, Reversibility, and Kinetic Models Acs Catalysis. 8: 4178-4188. DOI: 10.1021/Acscatal.8B00524 |
0.362 |
|
| 2017 |
Cueny ES, Johnson HC, Anding BJ, Landis CR. Mechanistic studies of hafnium-pyridyl amido catalyzed 1-octene polymerization and chain transfer using quench labeling methods. Journal of the American Chemical Society. PMID 28763618 DOI: 10.1021/Jacs.7B05729 |
0.796 |
|
| 2017 |
Eshon J, Landis CR, Schomaker JM. Regioselective Rh-Catalyzed Hydroformylation of 1,1,3-Trisubstituted Allenes Using BisDiazaPhos Ligand. The Journal of Organic Chemistry. PMID 28621533 DOI: 10.1021/Acs.Joc.7B01140 |
0.465 |
|
| 2017 |
Brezny AC, Landis CR. Unexpected CO Dependencies, Catalyst Speciation, and Single-Turnover Hydrogenolysis Studies of Hydroformylation via High Pressure NMR Spectroscopy. Journal of the American Chemical Society. PMID 28125782 DOI: 10.1021/Jacs.6B12533 |
0.828 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/Acs.Organomet.7B00475 |
0.79 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Wildt J, Brezny AC, Landis CR. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes Organometallics. 36: 3142-3151. DOI: 10.1021/acs.organomet.7b00475 |
0.33 |
|
| 2017 |
Dunn AL, Landis CR. Stopped-Flow NMR and Quantitative GPC Reveal Unexpected Complexities for the Mechanism of NHC-Catalyzed Lactide Polymerization Macromolecules. 50: 2267-2275. DOI: 10.1021/Acs.Macromol.6B02139 |
0.406 |
|
| 2016 |
Jones BR, Abrams ML, Landis CR, May SA, Campbell AN, Martinelli JR, Calvin JR. Scalable Synthesis of Enantiopure Bis-3,4-diazaphospholane Ligands for Asymmetric Catalysis. The Journal of Organic Chemistry. PMID 27787982 DOI: 10.1021/Acs.Joc.6B01915 |
0.725 |
|
| 2016 |
Foarta F, Landis CR. Condensation Oligomers with Sequence Control but without Coupling Reagents and Protecting Groups via Asymmetric Hydroformylation and Hydroacyloxylation. The Journal of Organic Chemistry. PMID 27766871 DOI: 10.1021/Acs.Joc.6B02210 |
0.44 |
|
| 2016 |
Dunn AL, Landis CR. Progress Toward Reaction Monitoring at Variable Temperatures: A New Stopped-Flow NMR Probe Design. Magnetic Resonance in Chemistry : Mrc. PMID 27718501 DOI: 10.1002/Mrc.4538 |
0.386 |
|
| 2016 |
Miles KC, Abrams ML, Landis CR, Stahl SS. KetoABNO/NOx Cocatalytic Aerobic Oxidation of Aldehydes to Carboxylic Acids and Access to α-Chiral Carboxylic Acids via Sequential Asymmetric Hydroformylation/Oxidation. Organic Letters. PMID 27410397 DOI: 10.1021/Acs.Orglett.6B01598 |
0.701 |
|
| 2016 |
Nelsen DL, Anding BJ, Sawicki JL, Christianson MD, Arriola DJ, Landis CR. Chromophore Quench-Labeling: An Approach to Quantifying Catalyst Speciation As Demonstrated for (EBI)ZrMe2/B(C6F5)3-Catalyzed Polymerization of 1-Hexene Acs Catalysis. 6: 7398-7408. DOI: 10.1021/Acscatal.6B01819 |
0.769 |
|
| 2016 |
Johnson MD, May SA, Calvin JR, Lambertus GR, Kokitkar PB, Landis CR, Jones BR, Abrams ML, Stout JR. Continuous Liquid Vapor Reactions Part 1: Design and Characterization of a Reactor for Asymmetric Hydroformylation Organic Process Research and Development. 20: 888-900. DOI: 10.1021/Acs.Oprd.5B00407 |
0.722 |
|
| 2016 |
Johnson MD, May SA, Calvin JR, Lambertus GR, Kokitkar PB, Landis CR, Jones BR, Abrams ML, Stout JR. Continuous Liquid Vapor Reactions Part 1: Design and Characterization of a Reactor for Asymmetric Hydroformylation Organic Process Research and Development. 20: 888-900. DOI: 10.1021/Acs.Oprd.5B00407 |
0.722 |
|
| 2016 |
Johnson MD, May SA, Calvin JR, Lambertus GR, Kokitkar PB, Landis CR, Jones BR, Abrams ML, Stout JR. Continuous Liquid Vapor Reactions Part 1: Design and Characterization of a Reactor for Asymmetric Hydroformylation Organic Process Research and Development. 20: 888-900. DOI: 10.1021/Acs.Oprd.5B00407 |
0.722 |
|
| 2016 |
Abrams ML, Buser JY, Calvin JR, Johnson MD, Jones BR, Lambertus G, Landis CR, Martinelli JR, May SA, McFarland AD, Stout JR. Continuous Liquid Vapor Reactions Part 2: Asymmetric Hydroformylation with Rhodium-Bisdiazaphos Catalysts in a Vertical Pipes-in-Series Reactor Organic Process Research and Development. 20: 901-910. DOI: 10.1021/Acs.Oprd.5B00406 |
0.717 |
|
| 2016 |
Abrams ML, Buser JY, Calvin JR, Johnson MD, Jones BR, Lambertus G, Landis CR, Martinelli JR, May SA, McFarland AD, Stout JR. Continuous Liquid Vapor Reactions Part 2: Asymmetric Hydroformylation with Rhodium-Bisdiazaphos Catalysts in a Vertical Pipes-in-Series Reactor Organic Process Research and Development. 20: 901-910. DOI: 10.1021/Acs.Oprd.5B00406 |
0.717 |
|
| 2016 |
Abrams ML, Buser JY, Calvin JR, Johnson MD, Jones BR, Lambertus G, Landis CR, Martinelli JR, May SA, McFarland AD, Stout JR. Continuous Liquid Vapor Reactions Part 2: Asymmetric Hydroformylation with Rhodium-Bisdiazaphos Catalysts in a Vertical Pipes-in-Series Reactor Organic Process Research and Development. 20: 901-910. DOI: 10.1021/Acs.Oprd.5B00406 |
0.717 |
|
| 2015 |
Beach NJ, Knapp SM, Landis CR. A reactor for high-throughput high-pressure nuclear magnetic resonance spectroscopy. The Review of Scientific Instruments. 86: 104101. PMID 26520969 DOI: 10.1063/1.4932676 |
0.568 |
|
| 2015 |
Nelsen ER, Brezny AC, Landis CR. Interception and Characterization of Catalyst Species in Rhodium Bis(diazaphospholane)-Catalyzed Hydroformylation of Octene, Vinyl Acetate, Allyl Cyanide, and 1-Phenyl-1,3-butadiene. Journal of the American Chemical Society. 137: 14208-19. PMID 26466510 DOI: 10.1021/Jacs.5B09858 |
0.797 |
|
| 2015 |
Liu HJ, Landis C, Raynaud C, Eisenstein O, Tilley TD. Donor-Promoted 1,2-Hydrogen Migration from Silicon to a Saturated Ruthenium Center and Access to Silaoxiranyl and Silaiminyl Complexes. Journal of the American Chemical Society. 137: 9186-94. PMID 26135519 DOI: 10.1021/Jacs.5B05571 |
0.34 |
|
| 2015 |
Landis CR. Organic chemistry. Construction and deconstruction of aldehydes by transfer hydroformylation. Science (New York, N.Y.). 347: 29-30. PMID 25554776 DOI: 10.1126/Science.Aaa2329 |
0.382 |
|
| 2014 |
Abrams ML, Foarta F, Landis CR. Asymmetric hydroformylation of Z-enamides and enol esters with rhodium-bisdiazaphos catalysts. Journal of the American Chemical Society. 136: 14583-8. PMID 25241657 DOI: 10.1021/Ja507701K |
0.761 |
|
| 2014 |
Adint TT, Landis CR. Immobilized bisdiazaphospholane catalysts for asymmetric hydroformylation. Journal of the American Chemical Society. 136: 7943-53. PMID 24742285 DOI: 10.1021/Ja501568K |
0.811 |
|
| 2014 |
Wong GW, Adint TT, Landis CR. Synthesis of (2R)‐3‐[[(1,1‐Dimethylethyl)dimethylsilyl]oxy]‐2‐methylpropanal by Rhodium‐Catalyzed Asymmetric Hydroformylation Organic Syntheses. 243-254. DOI: 10.1002/0471264229.Os089.24 |
0.764 |
|
| 2014 |
Wong GW, Landis CR. Highly enantioselective hydroformylation of alkenes by rhodium-diazaphospholane catalysts Aldrichimica Acta. 47: 29-38. |
0.645 |
|
| 2013 |
Nelsen ER, Landis CR. Interception and characterization of alkyl and acyl complexes in rhodium-catalyzed hydroformylation of styrene. Journal of the American Chemical Society. 135: 9636-9. PMID 23786304 DOI: 10.1021/Ja404799M |
0.798 |
|
| 2013 |
Adint TT, Wong GW, Landis CR. Libraries of bisdiazaphospholanes and optimization of rhodium-catalyzed enantioselective hydroformylation. The Journal of Organic Chemistry. 78: 4231-8. PMID 23581247 DOI: 10.1021/Jo400525W |
0.816 |
|
| 2013 |
Wong GW, Landis CR. Iterative asymmetric hydroformylation/Wittig olefination sequence. Angewandte Chemie (International Ed. in English). 52: 1564-7. PMID 23283707 DOI: 10.1002/Anie.201208819 |
0.57 |
|
| 2013 |
Tonks IA, Froese RD, Landis CR. Very low pressure Rh-catalyzed hydroformylation of styrene with (S,S,S-bisdiazaphos): Regioselectivity inversion and mechanistic insights Acs Catalysis. 3: 2905-2909. DOI: 10.1021/Cs400943S |
0.709 |
|
| 2012 |
Wong GW, Adint TT, Landis CR. Synthesis of (2r)-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]- 2-methylpropanal by rhodium-catalyzed asymmetric hydroformylation Organic Syntheses. 89: 243-254. DOI: 10.15227/orgsyn.089.0243 |
0.779 |
|
| 2012 |
Moscato BM, Zhu B, Landis CR. Mechanistic investigations into the behavior of a labeled zirconocene polymerization catalyst Organometallics. 31: 2097-2107. DOI: 10.1021/Om3000955 |
0.43 |
|
| 2011 |
Watkins AL, Landis CR. Regioselective rhodium-catalyzed hydroformylation of 1,3-dienes to highly enantioenriched β,γ-unsaturated aldehyes with diazaphospholane ligands. Organic Letters. 13: 164-7. PMID 21133397 DOI: 10.1021/Ol102797T |
0.736 |
|
| 2011 |
Froese RD, Landis CR, Watkins AL. Mechanistic aspects of selectivity in the hydroformylation of olefins catalyzed by rhodium bisdiazaphos complexes Acs National Meeting Book of Abstracts. |
0.647 |
|
| 2010 |
Moscato BM, Zhu B, Landis CR. GPC and ESI-MS analysis of labeled poly(1-hexene): rapid determination of initiated site counts during catalytic alkene polymerization reactions. Journal of the American Chemical Society. 132: 14352-4. PMID 20873793 DOI: 10.1021/Ja105775R |
0.368 |
|
| 2010 |
McDonald RI, Wong GW, Neupane RP, Stahl SS, Landis CR. Enantioselective hydroformylation of N-vinyl carboxamides, allyl carbamates, and allyl ethers using chiral diazaphospholane ligands. Journal of the American Chemical Society. 132: 14027-9. PMID 20845958 DOI: 10.1021/Ja106674N |
0.707 |
|
| 2010 |
Christianson MD, Tan EH, Landis CR. Stopped-flow NMR: determining the kinetics of [rac-(C2H4(1-indenyl)2)ZrMe][MeB(C6F5)3]-catalyzed polymerization of 1-hexene by direct observation. Journal of the American Chemical Society. 132: 11461-3. PMID 20672801 DOI: 10.1021/Ja105107Y |
0.781 |
|
| 2010 |
Watkins AL, Landis CR. Origin of pressure effects on regioselectivity and enantioselectivity in the rhodium-catalyzed hydroformylation of styrene with (S,S,S)-BisDiazaphos. Journal of the American Chemical Society. 132: 10306-17. PMID 20662513 DOI: 10.1021/Ja909619A |
0.673 |
|
| 2010 |
Popp BV, Morales CM, Landis CR, Stahl SS. Electronic structural comparison of the reactions of dioxygen and alkenes with nitrogen-chelated palladium(0). Inorganic Chemistry. 49: 8200-7. PMID 20604535 DOI: 10.1021/Ic100806W |
0.308 |
|
| 2010 |
Stahl S, Landis C, McDonald R, Wong G, Neupane R. Rhodium-Catalyzed Asymmetric Hydro-formylation Synfacts. 2010: 1390-1390. DOI: 10.1055/s-0030-1258892 |
0.651 |
|
| 2010 |
Stahl S, Landis C, McDonald R, Wong G, Neupane R. Rhodium-Catalyzed Asymmetric Hydro-formylation Synfacts. 2010: 1390-1390. DOI: 10.1055/s-0030-1258892 |
0.651 |
|
| 2010 |
Stahl S, Landis C, McDonald R, Wong G, Neupane R. Rhodium-Catalyzed Asymmetric Hydro-formylation Synfacts. 2010: 1390-1390. DOI: 10.1055/s-0030-1258892 |
0.651 |
|
| 2010 |
Stahl S, Landis C, McDonald R, Wong G, Neupane R. Rhodium-Catalyzed Asymmetric Hydro-formylation Synfacts. 2010: 1390-1390. DOI: 10.1055/s-0030-1258892 |
0.651 |
|
| 2009 |
Landis CR, Atesin TA, Froese RDJ, Watkins A. Origins of selectivity in Rh(bisdiazaphos)-catalyzed hydroformylation of styrene Acs National Meeting Book of Abstracts. |
0.639 |
|
| 2008 |
Watkins AL, Hashiguchi BG, Landis CR. Highly enantioselective hydroformylation of aryl alkenes with diazaphospholane ligands. Organic Letters. 10: 4553-6. PMID 18811170 DOI: 10.1021/Ol801723A |
0.814 |
|
| 2007 |
Klosin J, Landis CR. Ligands for practical rhodium-catalyzed asymmetric hydroformylation. Accounts of Chemical Research. 40: 1251-9. PMID 17997526 DOI: 10.1021/Ar7001039 |
0.394 |
|
| 2007 |
Thomas PJ, Axtell AT, Klosin J, Peng W, Rand CL, Clark TP, Landis CR, Abboud KA. Asymmetric hydroformylation of vinyl acetate: application in the synthesis of optically active isoxazolines and imidazoles. Organic Letters. 9: 2665-8. PMID 17555324 DOI: 10.1021/Ol070900L |
0.62 |
|
| 2007 |
Popp BV, Wendlandt JE, Landis CR, Stahl SS. Reaction of molecular oxygen with an NHC-coordinated Pd0 complex: computational insights and experimental implications. Angewandte Chemie (International Ed. in English). 46: 601-4. PMID 17154213 DOI: 10.1002/Anie.200603667 |
0.304 |
|
| 2007 |
Christianson MD, Landis CR. Generalized treatment of NMR spectra for rapid chemical reactions Concepts in Magnetic Resonance Part a: Bridging Education and Research. 30: 165-183. DOI: 10.1002/Cmr.A.20090 |
0.74 |
|
| 2007 |
Watkins A, Landis CR. Investigations into the mechanism of the rhodium catalyzed asymmetric hydroformylation of styrene Acs National Meeting Book of Abstracts. |
0.653 |
|
| 2006 |
Landis CR, Christianson MD. Metallocene-catalyzed alkene polymerization and the observation of Zr-allyls. Proceedings of the National Academy of Sciences of the United States of America. 103: 15349-54. PMID 17032772 DOI: 10.1073/Pnas.0602704103 |
0.801 |
|
| 2006 |
Huang H, Hughes RP, Landis CR, Rheingold AL. The simplest binary fluorocarbon as a ligand. Synthetic, spectroscopic, crystallographic, and computational studies of a molybdenum complex of terminally ligated carbon monofluoride (fluoromethylidyne). Journal of the American Chemical Society. 128: 7454-5. PMID 16756295 DOI: 10.1021/Ja062510K |
0.339 |
|
| 2006 |
Landis CR, Nelson RC, Jin W, Bowman AC. Synthesis, characterization, and transition-metal complexes of 3,4-diazaphospholanes Organometallics. 25: 1377-1391. DOI: 10.1021/Om050922G |
0.346 |
|
| 2005 |
Clark TP, Landis CR, Freed SL, Klosin J, Abboud KA. Highly active, regioselective, and enantioselective hydroformylation with Rh catalysts ligated by Bis-3,4-diazaphospholanes. Journal of the American Chemical Society. 127: 5040-2. PMID 15810837 DOI: 10.1021/Ja050148O |
0.678 |
|
| 2004 |
Popp BV, Thorman JL, Morales CM, Landis CR, Stahl SS. "Inverse-electron-demand" ligand substitution: experimental and computational insights into olefin exchange at palladium(0). Journal of the American Chemical Society. 126: 14832-42. PMID 15535709 DOI: 10.1021/Ja0459734 |
0.397 |
|
| 2004 |
Landis CR, Sillars DR, Batterton JM. Reactivity of secondary metallocene alkyls and the question of dormant sites in catalytic alkene polymerization. Journal of the American Chemical Society. 126: 8890-1. PMID 15264808 DOI: 10.1021/Ja047547O |
0.78 |
|
| 2004 |
Landis CR, Clark TP. Solid-phase synthesis of chiral 3,4-diazaphospholanes and their application to catalytic asymmetric allylic alkylation. Proceedings of the National Academy of Sciences of the United States of America. 101: 5428-32. PMID 14985503 DOI: 10.1073/Pnas.0307572100 |
0.7 |
|
| 2004 |
Clark T, Landis C. Recent developments in chiral phospholane chemistry Tetrahedron Asymmetry. 15: 2123-2137. DOI: 10.1016/J.Tetasy.2004.06.025 |
0.626 |
|
| 2003 |
Clark TP, Landis CR. Resolved chiral 3,4-diazaphospholanes and their application to catalytic asymmetric allylic alkylation. Journal of the American Chemical Society. 125: 11792-3. PMID 14505381 DOI: 10.1021/Ja036359F |
0.657 |
|
| 2003 |
Sillars DR, Landis CR. Catalytic propene polymerization: determination of propagation, termination, and epimerization kinetics by direct NMR observation of the (EBI)Zr(MeB(C6F5)3)propenyl catalyst species. Journal of the American Chemical Society. 125: 9894-5. PMID 12914431 DOI: 10.1021/Ja036393U |
0.814 |
|
| 2003 |
Clark RW, Guzei IA, Jin WC, Landis CR. A 1,2,4-diazaphospholane complex of rhodium. Acta Crystallographica. Section C, Crystal Structure Communications. 59: M144-5. PMID 12682395 DOI: 10.1107/S0108270103002142 |
0.423 |
|
| 2003 |
Landis CR, Rosaaen KA, Sillars DR. Direct observation of insertion events at rac-(C2H4(1-indenyl)2)Zr(MeB(C6F5)3)-polymeryl intermediates: distinction between continuous and intermittent propagation modes. Journal of the American Chemical Society. 125: 1710-1. PMID 12580591 DOI: 10.1021/Ja028070O |
0.753 |
|
| 2002 |
Landis CR, Rosaaen KA, Uddin J. Heavy-atom kinetic isotope effects, cocatalysts, and the propagation transition state for polymerization of 1-hexene using the rac-(C(2)H(4)(1-indenyl)(2))ZrMe(2) catalyst precursor. Journal of the American Chemical Society. 124: 12062-3. PMID 12371823 DOI: 10.1021/Ja026608K |
0.808 |
|
| 2002 |
White CB, Rosaaen KA, Landis CR. A rapid quenched-flow device for the study of homogeneous polymerization kinetics Review of Scientific Instruments. 73: 411. DOI: 10.1063/1.1431441 |
0.781 |
|
| 2002 |
Landis CR, Uddin J. Quantum mechanical modelling of alkene hydroformylation as catalyzed by xantphos-Rh complexes Dalton Transactions. 729-742. DOI: 10.1039/B108649A |
0.397 |
|
| 2001 |
Liu Z, Somsook E, White CB, Rosaaen KA, Landis CR. Kinetics of initiation, propagation, and termination for the [rac-(C(2)H(4)(1-indenyl)(2))ZrMe][MeB(C(6)F(5))(3)]-catalyzed polymerization of 1-hexene. Journal of the American Chemical Society. 123: 11193-207. PMID 11697962 DOI: 10.1021/Ja016072N |
0.792 |
|
| 2001 |
Landis CR, Jin W, Owen JS, Clark TP. Rapid Access to Diverse Arrays of Chiral 3,4-Diazaphospholanes We thank the Department of Energy, Office of Basic Energy Sciences for financial support of this work. All crystal-structure determinations were performed by Dr. Doug Powell or Dr. Ilyea Guzei. The cone-angle measurements were made with the gracious assistance of Dr. David White of the UNC-Wilmington. Angewandte Chemie (International Ed. in English). 40: 3432-3434. PMID 11592161 DOI: 10.1002/1521-3773(20010917)40:18<3432::Aid-Anie3432>3.0.Co;2-3 |
0.659 |
|
| 2001 |
Liu Z, Somsook E, Landis CR. A (2)H-labeling scheme for active-site counts in metallocene-catalyzed alkene polymerization. Journal of the American Chemical Society. 123: 2915-6. PMID 11456992 DOI: 10.1021/Ja0055918 |
0.653 |
|
| 2001 |
Feldgus S, Landis CR. Origin of enantioreversal in the rhodium-catalyzed asymmetric hydrogenation of prochiral enamides and the effect of the α-substituent Organometallics. 20: 2374-2386. DOI: 10.1021/Om010060T |
0.371 |
|
| 2000 |
Landis CR, Steven Feldgus. A Simple Model for the Origin of Enantioselection and the Anti "Lock-and-Key" Motif in Asymmetric Hydrogenation of Enamides as Catalyzed by Chiral Diphosphine Complexes of Rh(I) This work was supported by the National Science Foundation (CHE-9618497) and by the National Center for Supercomputer Applications under MCA99S017N and used the CRAY ORIGIN 2000 computer system at the NCSA. Angewandte Chemie (International Ed. in English). 39: 2863-2866. PMID 11027991 DOI: 10.1002/1521-3773(20000818)39:16<2863::Aid-Anie2863>3.0.Co;2-K |
0.386 |
|
| 2000 |
Landis CR, Sawyer RA, Somsook E. Synthesis and characterization of a chiral, aza-15-crown-5-functionalized ferrocenyldiphosphine ligand for asymmetric catalysis Organometallics. 19: 994-1001. DOI: 10.1021/Om990391U |
0.755 |
|
| 2000 |
Landis CR, Feldgus S, Uddin J, Wozniak CE, Moloy KG. Computational assessment of the effect of σ-π bonding synergy and reorganization energies on experimental trends in rhodium-phosphine bond enthalpies Organometallics. 19: 4878-4886. DOI: 10.1021/Om000544+ |
0.768 |
|
| 2000 |
Feldgus S, Landis CR. Large-scale computational modeling of [Rh(DuPHOS)]+-catalyzed hydrogenation of prochiral enamides: Reaction pathways and the origin of enantioselection Journal of the American Chemical Society. 122: 12714-12727. DOI: 10.1021/Ja0019373 |
0.426 |
|
| 1999 |
Landis CR, Hilfenhaus P, Feldgus S. Structures and reaction pathways in rhodium(I)-catalyzed hydrogenation of enamides: A model DFT study Journal of the American Chemical Society. 121: 8741-8754. DOI: 10.1021/Ja991606U |
0.802 |
|
| 1998 |
Kimmich BFM, Somsook E, Landis CR. Oxidative addition of dihydrogen to [Ir(bisphosphine)(1,5- cyclooctadiene)]BF4 complexes: Kinetic and thermodynamic selectivity Journal of the American Chemical Society. 120: 10115-10125. DOI: 10.1021/Ja981536B |
0.715 |
|
| 1998 |
Landis CR, Brauch TW. Probing the nature of H2 activation in catalytic asymmetric hydrogenation Inorganica Chimica Acta. 270: 285-297. DOI: 10.1016/S0020-1693(97)06101-X |
0.396 |
|
| 1997 |
Neyman KM, Nasluzov VA, Hahn J, Landis CR, Rösch N. Density Functional Study of N2Activation by Molybdenum(III) Complexes. Unusually Strong Relativistic Effects in 4d Metal Compounds Organometallics. 16: 995-1000. DOI: 10.1021/Om9607863 |
0.386 |
|
| 1997 |
Casey CP, Hallenbeck SL, Monty Wright J, Landis CR. Formation and spectroscopic characterization of chelated d0 yttrium(III)-alkyl-alkene complexes Journal of the American Chemical Society. 119: 9680-9690. DOI: 10.1021/Ja9632567 |
0.352 |
|
| 1997 |
Hahn J, Landis CR, Nasluzov VA, Neyman KM, Rösch N. Steric Effects on Dinitrogen Cleavage by Three-Coordinate Molybdenum(IH) Complexes: A Molecular Mechanics Study Inorganic Chemistry. 36: 3947-3951. DOI: 10.1021/Ic961466E |
0.337 |
|
| 1996 |
Landis CR, Cleveland T, Firman TK. Structure of W(CH3)6. Science (New York, N.Y.). 272: 182a. PMID 17791391 DOI: 10.1126/Science.272.5259.182A |
0.326 |
|
| 1996 |
Kimmich BFM, Landis CR, Powell DR. Synthesis and characterization of boron-containing ferrocenyl ligands for asymmetric catalysis Organometallics. 15: 4141-4146. DOI: 10.1021/Om960447+ |
0.435 |
|
| 1996 |
MacFarland DK, Landis CR. Synthesis and characterization of novel ligands designed for secondary interactions Organometallics. 15: 483-485. DOI: 10.1021/Om950819Z |
0.358 |
|
| 1995 |
Casey CP, Hallenbeck SL, Pollock DW, Landis CR. Synthesis and spectroscopic characterization of the d0 transition metal-alkyl-alkene complex Cp*2YCH2CH2C(CH3) 2CH=CH2 Journal of the American Chemical Society. 117: 9770-9771. DOI: 10.1021/Ja00143A026 |
0.314 |
|
| 1993 |
Giovannetti JS, Kelly CM, Landis CR. Molecular mechanics and NOE investigations of the solution structures of intermediates in the [Rh(chiral bisphosphine)]+-catalyzed hydrogenation of prochiral enamides Journal of the American Chemical Society. 115: 4040-4057. DOI: 10.1021/Ja00063A025 |
0.412 |
|
| 1990 |
McCulloch B, Halpern J, Thompson MR, Landis CR. Catalyst-substrate adducts in asymmetric catalytic hydrogenation. Crystal and molecular structure of rhodium [((R,R)-1,2-bis{phenyl-o-anisoylphosphino}ethane)(methyl (Z)-.beta.-propyl-.alpha.-acetamidoacrylate)] tetrafluoroborate [Rh(DIPAMP)(MPAA)]BF4 Organometallics. 9: 1392-1395. DOI: 10.1021/Om00119A006 |
0.518 |
|
| 1990 |
Schaad DR, Landis CR. Activation of amide N-H bonds by iron and ruthenium phosphine complexes Journal of the American Chemical Society. 112: 1628-1629. DOI: 10.1021/Ja00160A052 |
0.345 |
|
| 1989 |
Chan ASC, Landis CR. An improved rhodium-DIOP catalyst system for the homogeneous asymmetric hydrogenation of acetophenone Journal of Molecular Catalysis. 49: 165-173. DOI: 10.1016/0304-5102(89)80048-3 |
0.433 |
|
| 1987 |
Landis CR, Halpern J. Asymmetric hydrogenation of methyl (Z)-.alpha.-acetamidocinnamate catalyzed by [1,2-bis(phenyl-o-anisoyl)phosphino)ethane]rhodium(I): kinetics, mechanism and origin of enantioselection Journal of the American Chemical Society. 109: 1746-1754. DOI: 10.1021/Ja00240A025 |
0.515 |
|
| 1983 |
Landis CR, Halpern J. Homogeneous catalysis of arene hydrogenation by cationic rhodium arene complexes Organometallics. 2: 840-842. DOI: 10.1021/Om50001A010 |
0.525 |
|
| 1983 |
Landis CR, Halpern J. Cationic rhodium hydrogenation catalysts containing chelating diphosphine ligands: effect of chelate ring size Journal of Organometallic Chemistry. 250: 485-490. DOI: 10.1016/0022-328X(83)85071-2 |
0.613 |
|
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