Molecular recognition: Cyclobutane thymine diners as rigid two-site receptors
- 31 December 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (17), 2401-2404
- https://doi.org/10.1016/s0040-4039(00)97372-6
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Nucleotide base recognition: a macrocyclic receptor for adenine employing hydrogen bonding and aromatic stacking interactionsJournal of the American Chemical Society, 1989
- Carboxylic acid complexation by a synthetic analog of the "carboxylate-binding pocket" of vancomycinJournal of the American Chemical Society, 1988
- Molecular recognition of biologically interesting substrates: synthesis of an artificial receptor for barbiturates employing six hydrogen bondsJournal of the American Chemical Society, 1988
- Molecular recognition: Model studies with convergent functional groupsJournal of Molecular Recognition, 1988
- Nucleotide base recognition: ditopic binding of guanine to a macrocyclic receptor containing naphthyridine and naphthalene unitsJournal of the Chemical Society, Chemical Communications, 1988
- Induced fit in synthetic receptors: nucleotide base recognition by a molecular hingeJournal of the American Chemical Society, 1987
- Model Studies in Molecular RecognitionScience, 1987
- The hydrogen bond in molecular recognitionTrends in Biochemical Sciences, 1987
- Concave functionality: design of a phenol sticky hostJournal of the American Chemical Society, 1986
- Hydrogen-bond geometry in organic crystalsAccounts of Chemical Research, 1984