Synthesis, Characterization and Microwave-Promoted Catalytic Activity of Novel N-phenylbenzimidazolium Salts in Heck-Mizoroki and Suzuki-Miyaura Cross-Coupling Reactions under Mild Conditions
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[1] L. Wan,et al. A Novel System for the Suzuki Cross‐Coupling Reaction Catalyzed with Light Fluorous Palladium—NHC Complex. , 2013 .
[2] Shi Tang,et al. Palladium-catalyzed cross-coupling reaction of aryl(trialkyl)silanes with aryl nitriles , 2012 .
[3] L. Wan,et al. A novel system for the Suzuki cross-coupling reaction catalysed with light fluorous palladium–NHC complex , 2012 .
[4] Amália Monge-Marcet,et al. Recyclable Hybrid Silica‐Based Catalysts Derived from Pd–NHC Complexes for Suzuki, Heck and Sonogashira Reactions , 2012 .
[5] X. Gu. TBAF-Assisted Palladium-Catalyzed Suzuki Reaction in Water Under the Ligand and Base-Free Conditions , 2012 .
[6] G. R. Rosa,et al. NCP pincer palladacycle as a phosphine-free catalyst precursor for the Heck-Mizoroki coupling of aryl halides{ , 2012 .
[7] E. Ponzio,et al. Synthesis and Characterizations of LiSICON Li2Co2(MoO4)3 with Different Amounts of Starch , 2012 .
[8] Mats Larhed,et al. Evaluation of a Nonresonant Microwave Applicator for Continuous-Flow Chemistry Applications , 2012 .
[9] V. Ananikov,et al. Toward the Ideal Catalyst: From Atomic Centers to a “Cocktail” of Catalysts , 2012 .
[10] M. Akkurt,et al. Synthesis, characterization, and microwave-promoted catalytic activity of novel benzimidazole salts bearing silicon-containing substituents in Heck-Mizoroki and Suzuki-Miyaura cross-coupling reactions under aerobic conditions , 2012, Turkish Journal of Chemistry.
[11] Lei Zhu,et al. N-Heterocyclic carbene–Pd(II) complex derived from proline for the Mizoroki–Heck reaction in water , 2011 .
[12] N. Iranpoor,et al. Carbon–carbon bond formation via homocoupling reaction of substrates with a broad diversity in water using Pd(OAc)2 and agarose hydrogel as a bioorganic ligand, support and reductant , 2011 .
[13] B. Çetinkaya,et al. Influence of CH3 Substituents in Tetrahydropyrimidin-2-ylidene: σ-Donating Properties and in situ Catalytic Activities of Precursor Salts/Pd(OAc)2 System for C—C Coupling Reactions. , 2011 .
[14] O. Büyükgüngör,et al. Synthesis of 1-substituted benzimidazole metal complexes and structural characterization of dichlorobis(1-phenyl-1 H -benzimidazole- κN 3)cobalt(II) and dichlorobis (1-phenyl-1 H -benzimidazole- κN 3)zinc(II) , 2011 .
[15] M. Tahir,et al. Synthesis, microwave‐promoted catalytic activity in Suzuki–Miyaura cross‐coupling reactions and antimicrobial properties of novel benzimidazole salts bearing trimethylsilyl group , 2011 .
[16] S. Yalcin,et al. Synthesis, characterization and microwave‐assisted catalytic activity of novel benzimidazole salts bearing piperidine and morpholine moieties in Heck cross‐coupling reactions , 2011 .
[17] B. Çetinkaya,et al. Influence of CH3 substituents on tetrahydropyrimidin-2-ylidene: σ-donating properties and in situ catalytic activities of precursor salts/Pd(OAc)2 system for C–C coupling reactions , 2011 .
[18] Á. Molnár. Efficient, selective, and recyclable palladium catalysts in carbon-carbon coupling reactions. , 2011, Chemical reviews.
[19] Chun Liu,et al. Oxygen-promoted PdCl2-catalyzed ligand-free Suzuki reaction in aqueous media. , 2011, Organic & biomolecular chemistry.
[20] D. Alonso,et al. Oxime-Derived Palladacycles as Source of Palladium Nanoparticles , 2010 .
[21] H. Lee,et al. Efficient Heck Reactions Catalyzed by Palladium(0) and -(II) Complexes Bearing N-Heterocyclic Carbene and Amide Functionalities , 2010 .
[22] Ülkü Yılmaz,et al. Synthesis and microwave-assisted catalytic activity of novel bis-benzimidazole salts bearing furfuryl and thenyl moieties in Heck and Suzuki cross-coupling reactions , 2010 .
[23] K. Dawood,et al. Heck and Suzuki cross-couplings of aryl and heteroaryl bromides in water using a new palladium(II)-complex , 2010 .
[24] Ö. Metin,et al. New route to synthesis of PVP‐stabilized palladium(0) nanoclusters and their enhanced catalytic activity in Heck and Suzuki cross‐coupling reactions , 2009 .
[25] N. Leadbeater,et al. 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 , 2009 .
[26] C. Xi,et al. cis‐Fashioned Palladium(II) Complexes of 2‐Phenylbenzimidazole Ligands: Synthesis, Characterization, and Catalytic Behavior Towards Suzuki—Miyaura Reaction. , 2009 .
[27] M. Shi,et al. Elimination of an Alkyl Group from Imidazolium Salts: Imidazole-Coordinated Dinuclear Monodentate NHC–Palladium Complexes Driven by Self-Assembly and Their Application in the Heck Reaction , 2009 .
[28] S. Özkar,et al. Synthesis and characterizations of N,N,N′,N′-tetrakis (diphenylphosphino)ethylendiamine derivatives: Use of palladium(II) complex as pre-catalyst in Suzuki coupling and Heck reactions , 2009 .
[29] Arani Chanda,et al. Organic synthesis "on water". , 2009, Chemical reviews.
[30] C. Kappe,et al. Heterogeneous versus homogeneous palladium catalysts for ligandless mizoroki-heck reactions: a comparison of batch/microwave and continuous-flow processing. , 2009, Chemistry.
[31] W. Herrmann,et al. A new palladium(II) complex of a functionalized N-heterocyclic carbene : Synthesis, characterization and application in Suzuki-Miyaura cross-coupling reactions , 2008 .
[32] S. Nolan,et al. Well-defined N-heterocyclic carbenes-palladium(II) precatalysts for cross-coupling reactions. , 2008, Accounts of chemical research.
[33] C. Kappe,et al. Microwave-assisted one-pot diboration/Suzuki cross-couplings. A rapid route to tetrasubstituted alkenes , 2008 .
[34] E. V. D. Eycken,et al. Recent Developments in Microwave-Assisted, Transition-Metal-Catalysed C-C and C-N Bond-Forming Reactions , 2008 .
[35] K. Dawood. Microwave-Assisted Suzuki—Miyaura and Heck—Mizoroki Cross-Coupling Reactions of Aryl Chlorides and Bromides in Water Using Stable Benzothiazole-Based Palladium(II) Precatalysts. , 2008 .
[36] C. Kappe,et al. Microwave-assisted synthesis in water as solvent. , 2007, Chemical reviews.
[37] M. Organ,et al. Palladium complexes of N-heterocyclic carbenes as catalysts for cross-coupling reactions--a synthetic chemist's perspective. , 2007, Angewandte Chemie.
[38] Liang Chen,et al. Organic chemistry in water. , 2006, Chemical Society reviews.
[39] N. Leadbeater,et al. The Application of Organic Bases in Microwave-Promoted Suzuki Coupling Reactions in Water. , 2006 .
[40] C. Oliver Kappe,et al. The impact of microwave synthesis on drug discovery , 2006, Nature Reviews Drug Discovery.
[41] N. A. Bumagin,et al. An improved protocol for ligandless Suzuki–Miyaura coupling in water , 2006 .
[42] Jie Tang,et al. Palladium—Benzimidazolium Salt Catalyst Systems for Suzuki Coupling: Development of a Practical and Highly Active Palladium Catalyst System for Coupling of Aromatic Halides with Arylboronic Acids. , 2006 .
[43] I. Beletskaya,et al. Non-conventional methodologies for transition-metal catalysed carbon–carbon coupling: a critical overview. Part 2: The Suzuki reaction , 2005 .
[44] A. Suzuki. Carbon-carbon bonding made easy. , 2005, Chemical communications.
[45] S. Nolan,et al. Simple (Imidazol-2-ylidene)-Pd-acetate Complexes as Effective Precatalysts for Sterically Hindered Suzuki—Miyaura Couplings. , 2005 .
[46] I. Özdemir,et al. Benzimidazolin‐2‐ylidene–palladium‐catalysed coupling reactions of aryl halides , 2005 .
[47] N. Leadbeater,et al. Suzuki coupling of aryl chlorides with phenylboronic acid in water, using microwave heating with simultaneous cooling. , 2005, Organic letters.
[48] S. Nolan,et al. Simple (imidazol-2-ylidene)-Pd-acetate complexes as effective precatalysts for sterically hindered Suzuki-Miyaura couplings. , 2005, Organic letters.
[49] C. Kappe,et al. Controlled microwave heating in modern organic synthesis. , 2004, Angewandte Chemie.
[50] N. Leadbeater,et al. Ligand-free palladium catalysis of the Suzuki reaction in water using microwave heating. , 2002, Organic letters.
[51] J. G. Vries. The Heck reaction in the production of fine chemicals , 2001 .
[52] A. Hallberg,et al. Microwave-assisted high-speed chemistry: a new technique in drug discovery. , 2001, Drug discovery today.
[53] I. Beletskaya,et al. The heck reaction as a sharpening stone of palladium catalysis. , 2000, Chemical reviews.
[54] A. Hallberg,et al. Microwave-Promoted Palladium-Catalyzed Coupling Reactions , 1996 .
[55] Norio Miyaura,et al. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds , 1995 .
[56] P. Hitchcock,et al. Carbene complexes XXIV. Preparation and characterization of two enetetramine-derived carbenerhodium(I) chloride complexes RhCl(LR))3 and [RhCl(COD)LR] and the preparation and X-ray structures of the enetetramine L2R and its salt [L2R][BF4]2 , 1995 .
[57] P. Hitchcock,et al. Regular papersCarbene complexes: XXIV2. Preparation and characterization of two enetetramine-derived carbenerhodium(I) chloride complexes RhCl(LR)3 and [RhCl(COD)LR] and the preparation and X-ray structures of the enetetramine L2R and its salt [L2R][BF4]2 , 1994 .
[58] 施敏,et al. Elimination of an Alkyl Group from Imidazolium Salts: Imidazole-Coordinated Dinuclear Monodentate NHC-Palladium Complexes Driven by Self-Assembly and Their Application in the Heck Reaction , 2009 .
[59] M. Larhed,et al. Microwave-Assisted and Metal-Catalyzed Coupling Reactions , 2006 .
[60] S. Nolan. N-heterocyclic carbenes in synthesis , 2006 .
[61] P. Hitchcock,et al. Synthesis and structures of 1,3,1′,3′-tetrabenzyl-2,2′-biimidazolidinylidenes (electron-rich alkenes), their aminal intermediates and their degradation products , 1998 .
[62] G. Higgs. NOVEL TREATMENTS FOR ASTHMA , 1997 .
[63] P. Hitchcock,et al. CARBENE COMPLEXES. XXIV: PREPARATION AND CHARACTERIZATION OF TWO ENETETRAMINE-DERIVED CARBENERHODIUM(I) CHLORIDE COMPLEXES RHCL(LR)3 AND RHCL(COD)LR L R=DCN(ME)CU(CH)4CNME-O AND THE PREPARATION AND X-RAY STRUCTURES OF THE ENET ETRAMINE L2R AND ITS SALT L2RBF42 , 1994 .
[64] M. A. Phillips. CCCXVII.—The formation of 2-substituted benziminazoles , 1928 .