Efficient method for ring opening of epoxides with amines by NaY zeolite under solvent-free conditions

[1]  Toshio Suzuki,et al.  The first example of samarium diiodide-promoted intramolecular ketone-ester coupling of ketones tethering acyloxyalkyl side chains producing 2-hydroxy cyclic hemiacetals , 2006 .

[2]  A. Kamal,et al.  Copper(II) tetrafluoroborate-catalyzed ring-opening of epoxides by amines , 2005 .

[3]  A. Navarro,et al.  Opening of epoxides with aromatic amines promoted by indium tribromide: a mild and efficient method for the synthesis of β-amino alcohols , 2004 .

[4]  A. Chakraborti,et al.  An efficient synthesis of 2-amino alcohols by silica gel catalysed opening of epoxide rings by amines. , 2004, Organic & biomolecular chemistry.

[5]  Thierry Ollevier,et al.  Bismuth triflate-catalyzed mild and efficient epoxide opening by aromatic amines under aqueous conditions , 2004 .

[6]  A. Chakraborti,et al.  ZrCl4 as a new and efficient catalyst for the opening of epoxide rings by amines , 2003 .

[7]  A. I. Kozlov,et al.  Catalytic aminolysis of epoxide by alumina prepared from amine-protected Al precursor , 2003 .

[8]  J. Reedijk,et al.  Zinc-catalyzed aminolysis of epoxides , 2003 .

[9]  T. Akiyama,et al.  Brønsted Acid-Mediated Synthesis of α-Amino Phosphonates under Solvent-Free Conditions , 2003 .

[10]  H. Togo,et al.  Environmentally-Friendly Wohl-Ziegler Bromination: Ionic-Liquid Reaction and Solvent-Free Reaction , 2003 .

[11]  J. Yadav,et al.  [Bmim]BF4 ionic liquid: a novel reaction medium for the synthesis of β-amino alcohols , 2003 .

[12]  Thierry Ollevier,et al.  An efficient method for the ring opening of epoxides with aromatic amines catalyzed by bismuth trichloride , 2002 .

[13]  J. Desmurs,et al.  Regioselective ring opening of epoxides by nucleophiles mediated by lithium bistrifluoromethanesulfonimide , 2002 .

[14]  M. D. Pujol,et al.  Mild cleavage of aliphatic epoxides with substituted anilines on alumina , 2002 .

[15]  K. Nagaiah,et al.  Bi3+ CATALYZED REGIOSELECTIVE RING OPENING OF EPOXIDES WITH AROMATIC AMINES , 2002 .

[16]  M. Curini,et al.  Zirconium Sulfophenyl Phosphonate as a Heterogeneous Catalyst in the Preparation of β‐Amino Alcohols from Epoxides , 2001 .

[17]  V. Kesavan,et al.  Facile ring opening of oxiranes with aromatic amines in fluoro alcohols , 2000, The Journal of organic chemistry.

[18]  M. Clerici.  Zeolites for fine chemicals production , 2000 .

[19]  S. Bergmeier.  The Synthesis of Vicinal Amino Alcohols , 2000 .

[20]  J. Clark,et al.  Solid acids and their use as environmentally friendly catalysts in organic synthesis , 2000 .

[21]  S. Chandrasekhar,et al.  TaCl5-Catalyzed Cleavage of Epoxides with Aromatic Amines , 2000 .

[22]  K. Akamanchi,et al.  Diisopropoxyaluminium Trifluoroacetate: A New Promoter for Aminolysis of Epoxides , 2000 .

[23]  F. Ito,et al.  The preparation of β-substituted amines from mixtures of epoxide opening products via a common aziridinium ion intermediate , 1999 .

[24]  E. Corey,et al.  re- and si-Face-Selective Nitroaldol Reactions Catalyzed by a Rigid Chiral Quaternary Ammonium Salt: A Highly Stereoselective Synthesis of the HIV Protease Inhibitor Amprenavir (Vertex 478). , 1999, Angewandte Chemie.

[25]  Y. Hase,et al.  Catalytic Asymmetric Aminolysis of 3,5,8-Trioxabicyclo[5.1.0]octane Providing an Optically Pure 2-Amino-1,3,4-butanetriol Equivalent. , 1999, The Journal of organic chemistry.

[26]  G. Sekar,et al.  An Efficient Method for Cleavage of Epoxides with Aromatic Amines. , 1999, The Journal of organic chemistry.

[27]  M. R. Saidi,et al.  Microwave-assisted Aminolysis of Epoxides under Solvent-free Conditions Catalyzed by Montmorillonite Clay†: , 1999 .

[28]  A. Hoveyda,et al.  Zr-Catalyzed Kinetic Resolution of Allylic Ethers and Mo-Catalyzed Chromene Formation in Synthesis. Enantioselective Total Synthesis of the Antihypertensive Agent (S,R,R,R)-Nebivolol , 1998 .

[29]  P. Andersson,et al.  (1S,3R,4R)-2-Azanorbornylmethanol, an Efficient Ligand for Ruthenium-Catalyzed Asymmetric Transfer Hydrogenation of Ketones. , 1998, The Journal of organic chemistry.

[30]  A. Ganesan,et al.  Solution-phase synthesis of a -amino alcohol combinatorial library , 1997 .

[31]  Shi-hui Wu,et al.  A Regio-and Stereoselective Synthesis of β-Amino Alcohols , 1997 .

[32]  D. M. Hodgson,et al.  Enantioselective desymmetrisation of achiral epoxides , 1996 .

[33]  F. Leroy,et al.  Lithium trifluoromethanesulfonate-catalysed aminolysis of oxiranes , 1996 .

[34]  A. Riera,et al.  Ready access to stereodefined β-hydroxy-γ-amino acids. Enantioselective synthesis of fully protected cyclohexylstatine , 1996 .

[35]  D. Ager,et al.  1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis. , 1996, Chemical reviews.

[36]  Guigen Li,et al.  Catalytic Asymmetric Aminohydroxylation (AA) of Olefins , 1996 .

[37]  P. D. Weghe,et al.  RING OPENING REACTIONS OF EPOXIDES CATALYZED BY SAMARIUM IODIDES , 1995 .

[38]  M. Teraguchi,et al.  High-Pressure Promoted and Silica Gel Catalyzed Aminolysis of Epoxides with Glycine Esters , 1994 .

[39]  M. Pineschi,et al.  Lanthanide(III) trifluoromethanesulfonates as extraordinarily effective new catalysts for the aminolysis of 1,2-epoxides , 1994 .

[40]  Yoshinori Yamamoto,et al.  Ytterbium Triflate and High Pressure-Mediated Ring Opening of Epoxides with Amines. , 1994 .

[41]  Yoshinori Yamamoto,et al.  Regio- and stereo-selective ring opening of epoxides with amide cuprate reagents , 1993 .

[42]  R. M. Hanson.  The synthetic methodology of nonracemic glycidol and related 2,3-epoxy alcohols , 1991 .

[43]  Paolo Crotti,et al.  Metal salts as new catalysts for mild and efficient aminolysis of oxiranes , 1990 .

[44]  J. Iqbal,et al.  An unusual chemoselectivity in cobalt(II) chloride catalysed cleavage of oxiranes with anilines: A highly regioselective synthesis of β-amino alcohols , 1990 .

[45]  Yoshinori Yamamoto,et al.  Aminolead compounds as a new reagent for regioselective ring opening of epoxides , 1989 .

[46]  A. Baba,et al.  Tetraphenylstibonium triflate as a regio- and chemoselective catalyst in the reaction of oxiranes with amines , 1989 .

[47]  M. Carre,et al.  A convenient preparation of β-amino alcohols from epoxides and halomagnesium alkylamides , 1985 .

[48]  A. Papini,et al.  REGIOSPECIFIC CONVERSION OF OXIRANES, OXETANES, AND LACTONES INTO DIFUNCTIONAL NITROGEN COMPOUNDS VIA AMINOSILANES AND AMINOSTANNANES , 1984 .

[49]  J. Kirtane,et al.  Recent advances in the preparation and synthetic applications of oxiranes , 1983 .

[50]  L. Overman,et al.  Facile aminolysis of epoxides with diethylaluminum amides , 1981 .

[51]  J. Baldwin,et al.  Mode of nucleophilic addition to epichlorohydrin and related species: chiral aryloxymethyloxiranes , 1979 .

[52]  D. Z. Rogers,et al.  Organic reactions at alumina surfaces. Mild and selective opening of epoxides by alcohols, thiols, benzeneselenol, amines, and acetic acid , 1977 .

[53]  J. A. Deyrup,et al.  1,2,3-oxathiazolidines. Heterocyclic system , 1969 .

[54]  M. Freifelder,et al.  Effect of Nuclear Substitution on the Reaction of Aromatic Amines with Ethylene Oxide , 1961 .

[55]  R. S. Murphey,et al.  Secondary and tertiary amino ketones and alcohols derived from desoxybenzoin and 1,2-diphenylethanol; ring-chain tautomerism of the alpha-(beta-hydroxyethylamino) ketones. , 1948, Journal of the American Chemical Society.