Capture of reactive monophosphine-ligated palladium(0) intermediates by mass spectrometry.
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Edward C Sherer | Qinghao Chen | Roy Helmy | Christopher J Welch | C. Welch | E. Sherer | Qiuling Zheng | R. Helmy | Yong Liu | Qiuling Zheng | Yong Liu | Meihong Hu | Hao Chen | Qinghao Chen | Hao Chen | Meihong Hu
[1] J. White,et al. Synthesis, structure and gas-phase reactivity of a silver hydride complex [Ag3{(PPh2)2CH2}3(μ3-H)(μ3-Cl)]BF4. , 2013, Angewandte Chemie.
[2] J. Loo,et al. Direct ionization of large proteins and protein complexes by desorption electrospray ionization-mass spectrometry. , 2011, Analytical chemistry.
[3] Shiyong Wu,et al. The study of protein conformation in solution via direct sampling by desorption electrospray ionization mass spectrometry , 2010, Journal of the American Society for Mass Spectrometry.
[4] M. Beller,et al. Molecularly defined palladium(0) monophosphine complexes as catalysts for efficient cross-coupling of aryl chlorides and phenylboronic acid1 , 2000 .
[5] D. Feichtinger,et al. ZIEGLER-NATTA-LIKE OLEFIN OLIGOMERIZATION BY ALKYLZIRCONOCENE CATIONS IN AN ELECTROSPRAY IONIZATION TANDEM MASS SPECTROMETER , 1998 .
[6] J. Hartwig,et al. Effect of ligand steric properties and halide identity on the mechanism for oxidative addition of haloarenes to trialkylphosphine Pd(0) complexes. , 2009, Journal of the American Chemical Society.
[7] R. Zare,et al. Transient Ru-methyl formate intermediates generated with bifunctional transfer hydrogenation catalysts , 2012, Proceedings of the National Academy of Sciences.
[8] M. García‐Melchor,et al. Computational perspective on Pd-catalyzed C-C cross-coupling reaction mechanisms. , 2013, Accounts of chemical research.
[9] R. Zare,et al. Identification of fleeting electrochemical reaction intermediates using desorption electrospray ionization mass spectrometry. , 2015, Journal of the American Chemical Society.
[10] S. Buchwald,et al. N-Substituted 2-Aminobiphenylpalladium Methanesulfonate Precatalysts and Their Use in C–C and C–N Cross-Couplings , 2014, The Journal of organic chemistry.
[11] D. Plattner,et al. Direct Proof for OMnv (salen) Complexes , 1997 .
[12] B. Stoltz,et al. Gas-phase synthesis of charged copper and silver Fischer carbenes from diazomalonates: mechanistic and conformational considerations in metal-mediated wolff rearrangements. , 2003, Journal of the American Chemical Society.
[13] Allis S. Chien,et al. Detecting reaction intermediates in liquids on the millisecond time scale using desorption electrospray ionization. , 2011, Angewandte Chemie.
[14] S. Buchwald,et al. A new class of easily activated palladium precatalysts for facile C-N cross-coupling reactions and the low temperature oxidative addition of aryl chlorides. , 2008, Journal of the American Chemical Society.
[15] F. Schoenebeck,et al. Experiment and computation: a combined approach to study the reactivity of palladium complexes in oxidation states 0 to IV. , 2014, Chemical Society reviews.
[16] M. Rodgers,et al. Cation-pi interactions: structures and energetics of complexation of Na+ and K+ with the aromatic amino acids, phenylalanine, tyrosine, and tryptophan. , 2004, Journal of the American Chemical Society.
[17] K. Houk,et al. Ligand-controlled regioselectivity in palladium-catalyzed cross coupling reactions. , 2010, Journal of the American Chemical Society.
[18] D. A. Dougherty,et al. Cation-π Interactions in Chemistry and Biology: A New View of Benzene, Phe, Tyr, and Trp , 1996, Science.
[19] S. Buchwald,et al. Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands. , 2013, Organic letters.
[20] J. S. McIndoe,et al. Practical approaches to the ESI-MS analysis of catalytic reactions. , 2014, Journal of mass spectrometry : JMS.
[21] C. Amatore,et al. Identification of the Effective Palladium(0) Catalytic Species Generated in Situ from Mixtures of Pd(dba)2 and Bidentate Phosphine Ligands. Determination of Their Rates and Mechanism in Oxidative Addition , 1997 .
[22] M. Martinelli,et al. New catalysts for Suzuki-Miyaura coupling reactions of heteroatom-substituted heteroaryl chlorides. , 2007, The Journal of organic chemistry.
[23] P. Espinet,et al. Snapshots of a Stille reaction , 2001 .
[24] R. Cooks,et al. Mass Spectrometry Sampling Under Ambient Conditions with Desorption Electrospray Ionization , 2004, Science.
[25] V. Ananikov,et al. Pd2(dba)3 as a Precursor of Soluble Metal Complexes and Nanoparticles: Determination of Palladium Active Species for Catalysis and Synthesis , 2012 .
[26] Cory Valente,et al. Pd-catalyzed aryl amination mediated by well defined, N-heterocyclic carbene (NHC)-Pd precatalysts, PEPPSI. , 2008, Chemistry.
[27] M. Eberlin,et al. Probing the mechanism of the Heck reaction with arene diazonium salts by electrospray mass and tandem mass spectrometry. , 2004, Angewandte Chemie.
[28] S. Buchwald,et al. Biaryl phosphane ligands in palladium-catalyzed amination. , 2008, Angewandte Chemie.
[29] S. Messaoudi,et al. 2-Aminobiphenyl Palladacycles: The “Most Powerful” Precatalysts in C–C and C–Heteroatom Cross-Couplings , 2015 .
[30] Carin C. C. Johansson Seechurn,et al. Development of Preformed Pd Catalysts for Cross-Coupling Reactions, Beyond the 2010 Nobel Prize , 2012 .
[31] R. Vilar,et al. Monoligated palladium species as catalysts in cross-coupling reactions. , 2005, Angewandte Chemie.
[32] I. Beletskaya,et al. Palladacycles in catalysis – a critical survey , 2004 .
[33] R. O'hair,et al. Gas-phase synthesis and reactivity of the lithium acetate enolate anion, -CH2CO2Li. , 2009, Angewandte Chemie.
[34] M. Martinelli,et al. New air-stable catalysts for general and efficient suzuki-miyaura cross-coupling reactions of heteroaryl chlorides. , 2006, Organic letters.
[35] Stephen R. Wilson,et al. ESI-MS detection of ionic intermediates in phosphine-mediated reactions , 1993 .
[36] Pietro Vidossich,et al. Palladium monophosphine Pd(PPh3): is it really accessible in solution? , 2014, Chemical communications.
[37] S. Buchwald,et al. Design and Preparation of New Palladium Precatalysts for C-C and C-N Cross-Coupling Reactions. , 2012, Chemical science.
[38] S. Buchwald,et al. A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids. , 2010, Journal of the American Chemical Society.
[39] Gregori Ujaque,et al. A DFT Study of the Full Catalytic Cycle of the Suzuki−Miyaura Cross-Coupling on a Model System , 2006 .
[40] K. Ding,et al. Insight into the mechanism of the asymmetric ring-opening aminolysis of 4,4-dimethyl-3,5,8-trioxabicyclo[5.1.0]octane catalyzed by titanium/BINOLate/water system: evidence for the Ti(BINOLate)2-bearing active catalyst entities and the role of water. , 2008, Journal of the American Chemical Society.
[41] Krista L Vikse,et al. Oxidative Additions of Aryl Halides to Palladium Proceed through the Monoligated Complex , 2013 .
[42] S. Buchwald,et al. Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands. , 2008, Accounts of chemical research.
[43] J. Verkade,et al. Scope and limitations of Pd2(dba)3/P(i-BuNCH2CH2)3N-catalyzed Buchwald-Hartwig amination reactions of aryl chlorides. , 2004, The Journal of organic chemistry.
[44] D. A. Dougherty,et al. The Cationminus signpi Interaction. , 1997, Chemical reviews.
[45] J. Hartwig. Carbon–heteroatom bond formation catalysed by organometallic complexes , 2008, Nature.
[46] J. Harvey,et al. Computed ligand effects on the oxidative addition of phenyl halides to phosphine supported palladium(0) catalysts. , 2014, Dalton transactions.