Morphine recognition by a porphyrin–cyclocholate molecular bowl
- 1 January 1993
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 5,p. 456-458
- https://doi.org/10.1039/c39930000456
Abstract
A molecular bowl has been prepared by constructing a metalloporphyrin on one face of a tetrameric cyclocholate; the bowl selectively binds morphine by a combination of nitrogen–metal ligation and hydrogen bonding.Keywords
This publication has 12 references indexed in Scilit:
- Thermodynamic and kinetic data for macrocycle interaction with neutral moleculesChemical Reviews, 1992
- Cyclocholates: Synthesis and Ion BindingTetrahedron Letters, 1992
- Towards Synthetic Enzymes Based on Porphyrins and SteroidsPublished by Springer Nature ,1992
- Diastereo- and enantio-selective binding of octyl glucosides by an artificial receptorJournal of the Chemical Society, Chemical Communications, 1992
- Mit Donorzentren versehener korbförmiger Molekülhohlraum — Darstellung, Struktur, EigenschaftenEuropean Journal of Inorganic Chemistry, 1991
- Highly selective binding of simple peptides by a C3 macrotricyclic receptorJournal of the American Chemical Society, 1991
- New procedures for selectively protected cholic acid derivatives. Regioselective protection of the 12α-OH group, and t-butyl esterification of the carboxyl groupJournal of the Chemical Society, Perkin Transactions 1, 1990
- Chiral recognition in clefts and cyclophane cavities shaped by the 1,1'-binaphthyl major grooveThe Journal of Organic Chemistry, 1989
- Molecular recognition. 5. Molecular recognition of sugars via hydrogen-bonding interaction with a synthetic polyhydroxy macrocycleJournal of the American Chemical Society, 1989
- Korbförmige wirtmoleküle:Tetrahedron Letters, 1985