Synthesis of Chiral Tetraazacoronands Derived from l-Alanine and Their Investigations Using Capillary Electrophoresis Technique

[1]  U. Nilsson,et al.  An efficient and convergent route towards water-soluble, chiral and amphiphilic macrocycles , 2001 .

[2]  Michal M. Achmatowicz,et al.  The Simple Synthesis of Chiral Polyazaoxacoronands Derived from α-Amino Acids , 2000 .

[3]  Gawronski,et al.  Designing large triangular chiral macrocycles: efficient , 2000, The Journal of organic chemistry.

[4]  Michal M. Achmatowicz,et al.  Preparation of a new type of homochiral l-proline derived cyclam and their nickel(II) complexes , 2000 .

[5]  H. Zhao,et al.  Synthesis and characterization of pyridine-based polyamido-polyester optically active macrocycles and enantiomeric recognition for D- and L-amino acid methyl ester hydrochloride. , 2000, The Journal of organic chemistry.

[6]  T. Jira,et al.  Chiral separation of unmodified amino acids with non-aqueous capillary electrophoresis based on the ligand-exchange principle. , 2000, Journal of chromatography. A.

[7]  A. Szczepańska,et al.  A New Approach to the Synthesis of Chiral Tetraazacoronands Derived from L-Alanine , 2000 .

[8]  Xiao‐Qi Yu,et al.  Synthesis of New Cheral Macrocyclic Tetraoxo Polyamines Containing Pyridine Ring and Functional Arms , 1999 .

[9]  F. Gomez,et al.  Use of a partial-filling technique in affinity capillary electrophoresis for determining binding constants of ligands to receptors. , 1999, Journal of chromatography. A.

[10]  D. Gryko An Efficient Method for Preparation of Chiral Macrocyclic Bisamides Starting from Diol Derivatives of d-Mannitol and l-Tartaric Acid , 1999 .

[11]  I. Alfonso,et al.  Chemoenzymatic syntheses of two optically active hexa-azamacrocycles , 1999 .

[12]  D. Gryko,et al.  SYNTHETIC AND CRYSTALLOGRAPHIC STUDIES ON PYRIDINOPHANES , 1998 .

[13]  D. Gryko,et al.  The use of the Mitsunobu reaction in preparation of chiral synthons for macrocyclic frameworks , 1998 .

[14]  J. Biernat,et al.  Chromogenic proton-dissociable azocrown ether reagents for lithium ions , 1998 .

[15]  H. Nöth,et al.  Facile Synthesis of Cyclic Tetrapeptides from Nonactivated Peptide Esters on Metal Centers. , 1998, Angewandte Chemie.

[16]  V. Gupta,et al.  Determination of stability constants of Fe(II), Co(II) and Cu(II)-nitrilotriacetate-penicillamine mixed complexes by electrophoresis. , 1998, Talanta.

[17]  C. Chiou,et al.  Application of crown ethers as modifiers for the separation of amines by capillary electrophoresis , 1998 .

[18]  D. Gryko,et al.  Recent Advances in High Pressure Organic Synthesis , 1998 .

[19]  P. Prados,et al.  A preorganized macrocycle based on a bicyclic guanidinium subunit with six convergent hydrogen bonds for anion recognition , 1998 .

[20]  D. Gryko,et al.  The synthesis of macrocyclic diamides and tetramides containing phenol units , 1997 .

[21]  Kouji Nakamura,et al.  Separation of enantiomers and isomers of amino compounds by capillary electrophoresis and high-performance liquid chromatography utilizing crown ethers , 1997 .

[22]  J. Havel,et al.  Capillary electrophoretic estimation of sulfate stability constants of metal ions and determination of alkali and alkaline earth metals in waters , 1996 .

[23]  R. Eldik,et al.  Chemistry under extreme or non-classical conditions , 1996 .

[24]  K. Otsuka,et al.  Separation of enantiomers by capillary electrophoretic techniques , 1994 .

[25]  J. Jurczak,et al.  Synthesis of N,N′-dimethyl diazacoronands via double-quaternization reaction , 1993 .

[26]  P. Sałański,et al.  A new method for the synthesis of diazacoronands via double-amidation reaction , 1993 .

[27]  J. Jurczak,et al.  High Pressure Approach to the Synthesis of Diazacoronands and Cryptands , 1994 .

[28]  L. Hegedus,et al.  Synthesis of azapenams, diazepinones, and dioxocyclams via the photolytic reaction of chromium alkoxycarbene complexes with imidazolines , 1992 .

[29]  T. Wagler,et al.  Optically active difunctionalized dioxocyclam macrocycles: ligands for nickel-catalyzed oxidation of alkenes , 1989 .

[30]  J. Jurczak,et al.  High pressure chemical synthesis , 1989 .

[31]  J. Lehn,et al.  Polyaza-macrocycles of cyclophane type: Synthesis, structure of a chloroform inclusion complex and anion binding. , 1987 .

[32]  T. Wagler,et al.  Synthesis of an optically active C-funtiopnalized cyclam: (S)-5-(hydroxymethyl)-1,4,8,11-tetra-azacyclotetradecane and itws nickel(II) complex , 1987 .

[33]  K. A. Connors,et al.  Binding Constants: The Measurement of Molecular Complex Stability , 1987 .

[34]  R. Kellogg,et al.  SYNTHESIS OF AZA MACROCYCLES BY NUCLEOPHILIC RING-CLOSURE WITH CESIUM TOSYLAMIDES , 1984 .

[35]  J. Reisse,et al.  Solution thermodynamic studies. Part 6. Enthalpy-entropy compensation for the complexation reactions of some crown ethers with alkaline cations: a quantitative interpretation of the complexing properties of 18-crown-6 , 1982 .

[36]  G. J. Grant,et al.  Chiral cobalt(III) complexes of symmetrical hexaaza macrocycles , 1982 .

[37]  R. Appel,et al.  Dichlortris(dimethylamino)phosphoran als Dehydratisierungsreagenz zur Darstellung von Aktiv(-ONp, -OPcp, -ONSu)-estern N-geschützter multifunktioneller Aminosäuren , 1980 .

[38]  S. Kulstad,et al.  Diaza-crown ethers—VI : A mechanism for metal ion promoted formation of macrocyclic diazaoligoethers , 1980 .

[39]  Å. Åkeson,et al.  Diaza-crown Ethers. I. Alkali Ion Promoted Formation of Diaza-crown Ethers and Syntheses of Some N,N'-Disubstituted Derivatives. , 1979 .

[40]  I. Tabushi,et al.  Preparation of C-alkylated macrocyclic polyamines , 1977 .

[41]  Kent J. Voorhees,et al.  Flow synthesis. Substitute for the high-dilution steps in cryptate synthesis , 1973 .

[42]  A. Sevin,et al.  Cétones α cyclopropaniques dérivant de la (+) carvone. Etude de leur réduction : contrôle stéréoélectronique. , 1971 .

[43]  J. Clerc,et al.  Determination of H o , G o , and S o of the interaction of ions with carrier antibiotics by computerized microcalorimetry. , 1971, Helvetica chimica acta.

[44]  H. J. Backer,et al.  Condensation de la Benzile avec les Acides Oxy‐, Thio‐ et Sélénodiacétiques , 1940 .