Urea-tetrahydrobenzoxanthene receptors for carboxylic acids

[1]  Jong‐In Hong,et al.  Amino acid recognition of pyridine bis(oxazoline)–copper(II) complex in aqueous solvent , 2003 .

[2]  P. Prados,et al.  Enantioselective transport by a steroidal guanidinium receptor. , 2002, Chemistry.

[3]  A. I. Oliva,et al.  Enantioselective recognition of α-amino acid derivatives with a cis-tetrahydrobenzoxanthene receptor , 2002 .

[4]  J. Rebek,et al.  Molecular discrimination of N-protected amino acid esters by a self-assembled cylindrical capsule: spectroscopic and computational studies. , 2002, The Journal of organic chemistry.

[5]  Richard J. Fitzmaurice,et al.  Synthetic receptors for carboxylic acids and carboxylates , 2002 .

[6]  I. Stibor,et al.  Bis(amidopyridine)-linked calix[4]arenes: a novel type of receptor for dicarboxylic acids , 2002 .

[7]  H. Fukui,et al.  Synergistic binding and chirality sensing of unprotected amino acids with ferrocenecarboxylic acid–crown ether conjugate , 2001 .

[8]  A. D. Hamilton,et al.  Thermodynamic aspects of dicarboxylate recognition by simple artificial receptors. , 2001, The Journal of organic chemistry.

[9]  M. Hursthouse,et al.  Enantioselective amino acid recognition using acyclic thiourea receptors , 2001 .

[10]  A. P. Davis,et al.  Steroidal guanidines as enantioselective receptors for N-acyl α-amino acids. Part 1. 3α-Guanylated carbamates derived from cholic acid , 2001 .

[11]  L. Fielding Determination of Association Constants (Ka) from Solution NMR Data , 2000 .

[12]  T. Gelbrich,et al.  New macrobicyclic receptors for amino acids , 2000 .

[13]  C. Schmuck Carboxylate binding by 2-(guanidiniocarbonyl)pyrrole receptors in aqueous solvents: improving the binding properties of guanidinium cations through additional hydrogen bonds. , 2000, Chemistry.

[14]  Seongsoon Park,et al.  A metal complex that binds α-amino acids with high and predictable stereospecificity , 1999, Nature.

[15]  Heather Tye,et al.  Design, synthesis and preliminary studies on a novel class of chiral receptor for the recognition of amino acid derivatives1 , 1998 .

[16]  B. Snider Manganese(III)-Based Oxidative Free-Radical Cyclizations. , 1996, Chemical reviews.

[17]  T. H. Webb,et al.  Enantioselective and diastereoselective molecular recognition of neutral molecules , 1993 .

[18]  H. Whitlock,et al.  Concave functionality: design criteria for nonaqueous binding sites , 1990 .

[19]  M. Newcomb,et al.  Macrocycles Containing Tin. The Preparation of Macrobicyclic Lewis Acidic Hosts Containing Two Tin Atoms and 119-Sn NMR Studies of Their Chloride and Bromide Binding Properties in Solution , 1989 .

[20]  William H. Pirkle,et al.  Considerations of chiral recognition relevant to the liquid chromatography separation of enantiomers , 1989 .

[21]  D. Cram,et al.  The design of molecular hosts, guests, and their complexes , 1988, Science.

[22]  W. H. Pirkle,et al.  Chiral high-performance liquid chromatographic stationary phases. 1. Separation of the enantiomers of sulfoxides, amines, amino acids, alcohols, hydroxy acids, lactones, and mercaptans , 1979 .