BF3·SiO2: an efficient reagent system for the one-pot synthesis of 1,2,4,5-tetrasubstituted imidazoles
暂无分享,去创建一个
[1] M. Sekine,et al. Facile synthesis of 2′-O-cyanoethyluridine by ring-opening reaction of 2,2′-anhydrouridine with cyanoethyl trimethylsilyl ether in the presence of BF3·Et2O , 2007 .
[2] Meng‐Yang Chang,et al. BF3–OEt2-mediated rearrangement of 4-substituted-5,5-diphenylazepan-4-ols , 2007 .
[3] S. Kantevari,et al. Potassium dodecatugstocobaltate trihydrate (K5CoW12O40·3H2O): A mild and efficient reusable catalyst for the one-pot synthesis of 1,2,4,5-tetrasubstituted imidazoles under conventional heating and microwave irradiation , 2007 .
[4] S. Kantevari,et al. Highly efficient, one-pot, solvent-free synthesis of tetrasubstituted imidazoles using HClO4–SiO2 as novel heterogeneous catalyst , 2007 .
[5] V. Bansal,et al. One-pot synthesis of highly substituted imidazoles using molecular iodine : A versatile catalyst , 2007 .
[6] F. Bamoharram,et al. Highly efficient, four-component one-pot synthesis of tetrasubstituted imidazoles using Keggin-type heteropolyacids as green and reusable catalysts , 2007 .
[7] T. Klapötke,et al. γ-Alumina-supported boron trifluoride: Catalysis, radiotracer studies and computations , 2006 .
[8] A. Karimi,et al. Solvent-free synthesis of tetrasubstituted imidazoles on silica gel/NaHSO4 support , 2006 .
[9] M. A. Iglesias-Arteaga,et al. BF3·Et2O-induced Beckmann rearrangement of 23-hydroxyiminosapogenins. A shortcut to bisnorcholanic lactones , 2006 .
[10] N. Shankaraiah,et al. Selective reduction of aromatic azides in solution/solid-phase and resin cleavage by employing BF3·OEt2/EtSH. Preparation of DC-81 , 2006 .
[11] A. Hajipour,et al. Silica Sulfuric Acid as an Efficient Heterogeneous Catalyst for the Synthesis of 1,1-Diacetates under Solvent-Free Conditions , 2005 .
[12] M. Zolfigol,et al. Al(HSO4)3 as an efficient catalyst for acetalization of carbonyl compounds under heterogeneous or solvent -free conditions , 2005 .
[13] A. Hajipour,et al. A novel method for sulfonation of aromatic rings with silica sulfuric acid , 2004 .
[14] M. Hojo,et al. Alkylation of acetals using manganate–BF3·OEt2 mixed reagent , 2004 .
[15] Manoj Kumar,et al. BF3·Et2O promoted one-pot expeditious and convenient synthesis of 2-substituted benzimidazoles and 3,1,5-benzoxadiazepines , 2004 .
[16] C. Lindsley,et al. Efficient synthesis of imidazoles from aldehydes and 1,2-diketones using microwave irradiation. , 2004, Organic letters.
[17] M. Zolfigol,et al. The use of Nafion-H® as an efficient catalyst for the direct conversion of primary and secondary trimethylsilyl ethers to their corresponding ethers under mild and heterogeneous conditions , 2003 .
[18] M. Zolfigol,et al. Silica Sulfuric Acid: An Efficient Catalyst for the Direct Conversion of Primary and Secondary Trimethylsilyl Ethers to their Corresponding Ethers under Mild and Heterogeneous Conditions , 2003 .
[19] I. Mohammadpoor‐Baltork,et al. Regeneration of carbonyl compounds by cleavage of CN bonds under mild and completely heterogeneous conditions , 2003 .
[20] M. Zolfigol,et al. The use of Nafion-H®/NaNO2 as an efficient procedure for the chemoselective N-nitrosation of secondary amines under mild and heterogeneous conditions , 2003 .
[21] Jiling. Huang,et al. Syndiospecific polymerization of styrene catalyzed in situ by alkoxyl substituted half-sandwich titanocene and BF3·Et2O , 2003 .
[22] U. Bora,et al. A novel microwave-mediated one-pot synthesis of indolizines via a three-component reaction. , 2003, Organic letters.
[23] E. Toone,et al. Regioselective reduction of 4,6-O-benzylidenes using triethylsilane and BF3·Et2O , 2000 .
[24] S. Balalaie,et al. One-pot synthesis of tetrasubstituted imidazoles catalyzed by zeolite HY and silica gel under microwave irradiation , 2000 .
[25] P. Eilbracht,et al. Tandem Reaction Sequences under Hydroformylation Conditions: New Synthetic Applications of Transition Metal Catalysis. , 1999, Chemical reviews.
[26] Michael Almstetter,et al. Discovery of New Multi Component Reactions with Combinatorial Methods , 1999 .
[27] J. Yadav,et al. An expedient and highly selective conversion of alcohols to azides using a NaN 3 /BF 3 ·Et 2 O system , 1998 .
[28] J. Sisko. A One-Pot Synthesis of 1-(2,2,6,6-tetramethyl-4-piperidinyl)-4- (4-fluorophenyl)-5-(2-amino-4-pyrimidinyl)- imidazole: A Potent Inhibitor of P38 MAP Kinase , 1998 .
[29] J. Fortunak,et al. A New Regioselective Synthesis of 1,2,5-Trisubstituted 1H-Imidazoles and Its Application to the Development of Eprosartan. , 1997, The Journal of organic chemistry.
[30] T. Fukui,et al. A Novel Synthesis of Methyl 1,5-Disubstituted Imidazole-4-carboxylates Using 3-Bromo-2-isocyanoacrylates (BICA) , 1994 .
[31] G. Büchi,et al. A two-step synthesis of imidazoles from aldehydes via 4-tosyloxazolines , 1994 .
[32] Wei Zhang,et al. Synthesis of imidazoles via hetero-Cope rearrangements , 1993 .
[33] L. A. Reiter. Synthesis of 4(5)-acyl-, 1-substituted 5-acyl-, and 1-substituted 4-acyl-1H-imidazoles from 4-aminoisoxazoles , 1987 .