Effect of Electronic Enrichment of NHCs on the Catalytic Activity of [Pd(NHC)(acac)Cl] in Buchwald–Hartwig Coupling
暂无分享,去创建一个
[1] A. Slawin,et al. Large yet flexible N-heterocyclic carbene ligands for palladium catalysis. , 2013, Chemistry.
[2] S. Nolan,et al. A New Synthetic Route to p-Methoxy-2,6-disubstituted Anilines and their Conversion into N-Heterocyclic Carbene Precursors , 2013, Synlett.
[3] R. Rogers,et al. Trineopentylphosphine: a conformationally flexible ligand for the coupling of sterically demanding substrates in the Buchwald-Hartwig amination and Suzuki-Miyaura reaction. , 2013, The Journal of organic chemistry.
[4] A. Slawin,et al. [Pd(IPr*OMe)(acac)Cl] : tuning the N-heterocyclic carbene in catalytic C-N bond formation , 2013 .
[5] A. Slawin,et al. [Pd(IPr*)(3-Cl-pyridinyl)Cl2]: A Novel and Efficient PEPPSI Precatalyst , 2012 .
[6] M. Stradiotto,et al. Addressing challenges in palladium-catalyzed cross-coupling reactions through ligand design. , 2012, Chemistry.
[7] S. Nolan,et al. An Efficient Palladium‐NHC (NHC=N‐Heterocyclic Carbene) and Aryl Amination Pre‐Catalyst: [Pd(IPr*)(cinnamyl)Cl] , 2012 .
[8] Victor Snieckus,et al. Palladium-catalyzed cross-coupling: a historical contextual perspective to the 2010 Nobel Prize. , 2012, Angewandte Chemie.
[9] Carin C. C. Johansson Seechurn,et al. Development of Preformed Pd Catalysts for Cross-Coupling Reactions, Beyond the 2010 Nobel Prize , 2012 .
[10] A. Slawin,et al. [Pd(IPr*)(acac)Cl]: An Easily Synthesized, Bulky Precatalyst for C–N Bond Formation , 2012 .
[11] Ka Hou Hoi,et al. Amination with Pd-NHC complexes: rate and computational studies involving substituted aniline substrates. , 2012, Chemistry.
[12] S. Nolan,et al. N-Heterocyclic carbene (NHC) ligands and palladium in homogeneous cross-coupling catalysis: a perfect union. , 2011, Chemical Society reviews.
[13] J. Mata,et al. Recent Developments in the Applications of Palladium Complexes Bearing N-Heterocyclic Carbene Ligands , 2011 .
[14] Ka Hou Hoi,et al. Amination with Pd-NHC complexes: rate and computational studies on the effects of the oxidative addition partner. , 2011, Chemistry.
[15] S. Buchwald,et al. A multiligand based Pd catalyst for C-N cross-coupling reactions. , 2010, Journal of the American Chemical Society.
[16] F. Glorius,et al. The measure of all rings--N-heterocyclic carbenes. , 2010, Angewandte Chemie.
[17] S. Buchwald,et al. Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide. , 2010, Chemical science.
[18] A. Spek,et al. IPr* an easily accessible highly hindered N-heterocyclic carbene. , 2010, Dalton transactions.
[19] S. Nolan,et al. A comparative study on (NHC)Pd(acac)Cl complexes (NHC = N-heterocyclic carbene): indications for the origin of the different reactivity of saturated and unsaturated NHC in cross-coupling reactions , 2009 .
[20] J. Hartwig. Evolution of a fourth generation catalyst for the amination and thioetherification of aryl halides. , 2008, Accounts of chemical research.
[21] T. Ogata,et al. Palladium-catalyzed amination of aryl and heteroaryl tosylates at room temperature. , 2008, Journal of the American Chemical Society.
[22] S. Buchwald,et al. A highly active catalyst for Pd-catalyzed amination reactions: cross-coupling reactions using aryl mesylates and the highly selective monoarylation of primary amines using aryl chlorides. , 2008, Journal of the American Chemical Society.
[23] S. Nolan,et al. Well-defined N-heterocyclic carbenes-palladium(II) precatalysts for cross-coupling reactions. , 2008, Accounts of chemical research.
[24] C. So,et al. Palladium-catalyzed amination of aryl mesylates. , 2008, Angewandte Chemie.
[25] S. Buchwald,et al. Biaryl phosphane ligands in palladium-catalyzed amination. , 2008, Angewandte Chemie.
[26] Richard J. Fitzmaurice,et al. Development of a practical Buchwald-Hartwig amine arylation protocol using a conveniently prepared (NHC)Pd(R-allyl)Cl catalyst. , 2008, Organic & biomolecular chemistry.
[27] T. Ogata,et al. Highly reactive, general and long-lived catalysts for palladium-catalyzed amination of heteroaryl and aryl chlorides, bromides, and iodides: scope and structure-activity relationships. , 2008, Journal of the American Chemical Society.
[28] Cory Valente,et al. Pd-catalyzed aryl amination mediated by well defined, N-heterocyclic carbene (NHC)-Pd precatalysts, PEPPSI. , 2008, Chemistry.
[29] M. Organ,et al. Palladium complexes of N-heterocyclic carbenes as catalysts for cross-coupling reactions--a synthetic chemist's perspective. , 2007, Angewandte Chemie.
[30] Jianguo Mei,et al. Rapid room temperature Buchwald-Hartwig and Suzuki-Miyaura couplings of heteroaromatic compounds employing low catalyst loadings. , 2006, Chemistry.
[31] D. Dixon,et al. Bulky alkylphosphines with neopentyl substituents as ligands in the amination of aryl bromides and chlorides. , 2006, The Journal of organic chemistry.
[32] Xumu Zhang,et al. Triazole-based monophosphine ligands for palladium-catalyzed cross-coupling reactions of aryl chlorides. , 2006, The Journal of organic chemistry.
[33] Nicolas Marion,et al. (IPr)Pd(acac)Cl: an easily synthesized, efficient, and versatile precatalyst for C-N and C-C bond formation. , 2006, The Journal of organic chemistry.
[34] Jianguo Mei,et al. Modified (NHC)Pd(allyl)Cl (NHC = N-heterocyclic carbene) complexes for room-temperature Suzuki-Miyaura and Buchwald-Hartwig reactions. , 2006, Journal of the American Chemical Society.
[35] S. Nolan,et al. Synthesis of novel (NHC)Pd(acac)Cl complexes (acac=acetylacetonate) and their activity in cross-coupling reactions , 2005 .
[36] Xumu Zhang,et al. Triazole-based monophosphines for Suzuki-Miyaura coupling and amination reactions of aryl chlorides. , 2005, Organic letters.
[37] S. Buchwald,et al. Efficient pd-catalyzed amination of heteroaryl halides. , 2005, Organic letters.
[38] M. Organ,et al. Electronic nature of N-heterocyclic carbene ligands: effect on the Suzuki reaction. , 2005, Organic letters.
[39] S. Shekhar,et al. Highly reactive, general, and long-lived catalysts for coupling heteroaryl and aryl chlorides with primary nitrogen nucleophiles. , 2005, Angewandte Chemie.
[40] F. Glorius,et al. Sterically demanding, bioxazoline-derived N-heterocyclic carbene ligands with restricted flexibility for catalysis. , 2004, Journal of the American Chemical Society.
[41] F. Diederich,et al. Book review: Metal-catalyzed cross-coupling reactions. F. Diederich and P. J. Stang (eds) Wiley–VCH, Weinheim, 1998. xxi + 517 pages, £85 ISBN 3–527–29421–X , 1998 .
[42] M. Beller,et al. New ligands for a general palladium-catalyzed amination of aryl and heteroaryl chlorides. , 2004, Chemistry.
[43] F. Glorius,et al. An N-heterocyclic carbene ligand with flexible steric bulk allows Suzuki cross-coupling of sterically hindered aryl chlorides at room temperature. , 2003, Angewandte Chemie.
[44] S. Nolan,et al. Synthesis, characterization, and catalytic activity of N-heterocyclic carbene (NHC) palladacycle complexes. , 2003, Organic letters.
[45] S. Nolan,et al. Activation and Reactivity of (NHC)Pd(allyl)Cl (NHC = N-Heterocyclic Carbene) Complexes in Cross-Coupling Reactions , 2002 .
[46] S. Nolan,et al. An air-stable palladium/N-heterocyclic carbene complex and its reactivity in aryl amination. , 2002, Organic letters.
[47] S. Nolan,et al. Amination reactions of aryl halides with nitrogen-containing reagents mediated by palladium/imidazolium salt systems. , 2001, The Journal of organic chemistry.
[48] S. Stauffer,et al. High turnover number and rapid, room-temperature amination of chloroarenes using saturated carbene ligands. , 2000, Organic letters.
[49] S. Nolan,et al. Efficient Cross-Coupling of Aryl Chlorides with Aryl Grignard Reagents (Kumada Reaction) Mediated by a Palladium/Imidazolium Chloride System , 1999 .
[50] S. Nolan,et al. General and efficient catalytic amination of aryl chlorides using a palladium/bulky nucleophilic carbene system , 1999 .
[51] S. Buchwald,et al. A Simple Catalytic Method for the Conversion of Aryl Bromides to Arylamines , 1995 .
[52] J. Hartwig,et al. Palladium-catalyzed synthesis of arylamines from aryl halides. Mechanistic studies lead to coupling in the absence of tin reagents , 1995 .
[53] M. Kosugi,,et al. PALLADIUM-CATALYZED AROMATIC AMINATION OF ARYL BROMIDES WITH N,N-DI-ETHYLAMINO-TRIBUTYLTIN , 1983 .
[54] S. Buchwald,et al. Practical Palladium Catalysts for C-N and C-O Bond Formation , 2002 .