Lithium bromide catalyzed solvent free method for synthesis of 2-substituted benzimidazoles and imidazopyridines

[1]  J. S. Sandhu,et al.  LiBr: A Mild Lewis Acid Catalyst for Efficient One-Pot Synthesis of α-Amino Nitriles , 2008 .

[2]  M. A. Paesha,et al.  LiBr‐Catalyzed Simple and Efficient Synthesis of Some Novel Substituted Quinolines via Friedlander Heteroannulation Reaction , 2007 .

[3]  Huiqiang Ma,et al.  A simple and efficient method for synthesis of benzimidazoles using FeBr3 or Fe(NO3)3・9H2O as catalyst , 2007 .

[4]  K. Bahrami,et al.  A Simple and Efficient One-Pot Synthesis of 2-Substituted Benzimidazoles , 2007 .

[5]  A. Nasreen,et al.  l-Proline catalyzed selective synthesis of 2-aryl-1-arylmethyl-1H-benzimidazoles ☆ , 2007 .

[6]  B. Das,et al.  Efficient (bromodimethyl)sulfonium bromide mediated synthesis of benzimidazoles , 2007 .

[7]  Tong‐Shuang Li,et al.  A Highly Effective Sulfamic Acid/Methanol Catalytic System for the Synthesis of Benzimidazole Derivatives at Room Temperature , 2007 .

[8]  Feng Xu,et al.  Rapid One‐Pot Preparation of 2‐Substituted Benzimidazoles from Esters using Microwave Conditions , 2006 .

[9]  王玉炉,et al.  A simple KHSO4 promoted synthesis of 2-arylsubstituted benzimidazoles by oxidative condensation of aldehydes with o-phenylenediamine , 2006 .

[10]  G. Rezanejade Bardajee,et al.  Facile and Efficient One‐Pot Protocol for the Synthesis of Benzoxazole and Benzothiazole Derivatives using Molecular Iodine as Catalyst , 2006 .

[11]  A. Sudalai,et al.  NaIO4-mediated selective oxidation of alkylarenes and benzylic bromides/alcohols to carbonyl derivatives using water as solvent. , 2006, The Journal of organic chemistry.

[12]  P. Sun,et al.  The convenient synthesis of benzimidazole derivatives catalyzed by I2 in aqueous media , 2006 .

[13]  D. Shinde,et al.  BF3•OEt2 Promoted Solvent-free Synthesis of Benzimidazole Derivatives , 2006 .

[14]  D. Shinde,et al.  Zirconyl(IV) chloride-promoted synthesis of benzimidazole derivatives , 2006 .

[15]  R. Gibbs,et al.  A convenient one-pot synthesis of 2-substituted benzimidazoles , 2006 .

[16]  P. Gogoi,et al.  An efficient and one-pot synthesis of imidazolines and benzimidazoles via anaerobic oxidation of carbon–nitrogen bonds in water , 2006 .

[17]  A. Itoh,et al.  Aerobic Photooxidation of Methyl Group at Aromatic Nucleus with LiBr , 2005 .

[18]  Di Chen Synthesis of β-Benzylsulfanyl-β-trifluoromethyl-α-amino Acids Via Michael Addition in the Presence of Et3N/LiBr , 2005 .

[19]  H. Tian,et al.  An Efficient Procedure for the Synthesis of Benzimidazole Derivatives Using Yb(OTf)3 as Catalyst Under Solvent‐Free Conditions , 2004 .

[20]  T. Itoh,et al.  Synthesis of 2-Arylbenzothiazoles and Imidazoles Using Scandium Triflate as a Catalyst for Both a Ring Closing and an Oxidation Steps , 2004 .

[21]  T. Itoh,et al.  Synthesis of 2-Arylbenzothiazoles from 2-Aminobenzenethiol and Aryl Aldehydes Catalyzed by Scandium Triflate , 2004 .

[22]  C. Brain,et al.  An improved procedure for the synthesis of benzimidazoles, using palladium-catalyzed aryl-amination chemistry. , 2003, The Journal of organic chemistry.

[23]  M. Soufiaoui,et al.  Synthèse chimiosélective des benzimidazoles sur silice traitée par le chlorure du thionyle , 2003 .

[24]  A. J. Blake,et al.  Synthesis of benzimidazoles in high-temperature water , 2003 .

[25]  C. Brain,et al.  An intramolecular palladium-catalysed aryl amination reaction to produce benzimidazoles , 2002 .

[26]  Jun Lu,et al.  MICROWAVE IRRADIATION SYNTHESIS OF 2-SUBSTITUTED BENZIMIDAZOLES USING PPA AS A CATALYST UNDER SOLVENT-FREE CONDITIONS , 2002 .

[27]  L. Scott,et al.  Esomeprazole , 2012, Drugs.

[28]  S. C. Roy,et al.  An efficient chemo and regioselective oxidative nuclear bromination of activated aromatic compounds using lithium bromide and ceric ammonium nitrate , 2001 .

[29]  G. Parkinson,et al.  A new class of symmetric bisbenzimidazole-based DNA minor groove-binding agents showing antitumor activity. , 2001, Journal of medicinal chemistry.

[30]  M. Ghassemzadeh,et al.  Zeolite-induced Heterocyclization: A Superior Method of Synthesis of Condensed Imidazoles† , 2000 .

[31]  H. Al-Muhaimeed A Parallel-Group Comparison of Astemizole and Loratadine for the Treatment of Perennial Allergic Rhinitis , 1997, The Journal of international medical research.

[32]  D. Villemin,et al.  Clay Catalysis: Condensation of Orthoesters with O-Substituted Aminoaromatics into Heterocycles , 1996 .

[33]  M. Soufiaoui,et al.  Nouvelle voie de synthèse des arylimidazoles sous irradiation micro-ondes en “milieu sec” , 1995 .

[34]  S. Ōmura,et al.  Synthesis and biological activity of new 3-hydroxy-3-methylglutaryl-CoA synthase inhibitors: 2-oxetanones with a side chain mimicking the extended structure of 1233A. , 1994, Chemical & pharmaceutical bulletin.

[35]  L. Pérez-García,et al.  An Advantageous Synthesis of 2-Substituted Benzimidazoles Using Polyphosphoric Acid. 2-(Pyridyl)-1H-benzimidazoles, 1-Alkyl-(1H-benzimidazol-2-yl)pyridinium Salts, their Homologues and Vinylogues , 1992 .

[36]  E. Bouwman,et al.  Model systems for type I copper proteins: structures of copper coordination compounds with thioether and azole-containing ligands , 1990 .

[37]  M. A. Pujar,et al.  Cobalt(II), nickel(II) and copper(II) complexes of bidentate bibenzimidazoles , 1988 .

[38]  P. Nicholls,et al.  INTERACTION OF ETHOSUXIMIDE AND SODIUM VALPROATE IN MICE , 1986 .

[39]  M. Raban,et al.  Stereochemistry in trivalent nitrogen compounds. 42. N-(Arylthio)benzimidazoles. Torsional barriers and 1,3 rearrangement , 1985 .

[40]  H. Ziffer,et al.  Effect of ring size and methyl substituents on lithium bromide-catalyzed rearrangements of aryloxiranes , 1982 .

[41]  M. Montury,et al.  New Preparation of Bromoallenes , 1981 .