Cholesterol as a versatile platform for chiral recognition
- 1 January 1995
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 51 (2) , 555-566
- https://doi.org/10.1016/0040-4020(94)00915-h
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Chiral Recognition of α-Amino Acid Derivatives by a Steroidal Crown Ether at the Air-Water InterfaceChemistry Letters, 1994
- Sol-Gel Phase Transition of Switch-Functionalized Cholesterols as Detected by Circular DichroismChemistry Letters, 1992
- Synthesis and enantioselective coloration of optically active azophenolic acerands incorporating two 1,1′-binaphthyl moieties as the chiral centreJournal of the Chemical Society, Chemical Communications, 1992
- Molecular Recognition of Barbiturates by Diaminotriazine Functionalized MonolayersChemistry Letters, 1991
- Chirality Recognition by a Color Change in Crowned Cholesteric Liquid CrystalsChemistry Letters, 1991
- Syntheses and thermal properties of new liquid crystals bearing a crown ether ring: cation binding in the nematic phaseThe Journal of Organic Chemistry, 1990
- Crown–metal interactions in cholesteric liquid crystalsJournal of the Chemical Society, Chemical Communications, 1990
- Ion permeation through polymer-supported steroidal crown membranesJournal of Polymer Science Part C: Polymer Letters, 1989
- Stereochemistry and molecular recognition in "two dimensions"Accounts of Chemical Research, 1989
- Organic reactions in liquid crystalline solvents. 6. Regiochemical control of bimolecular chemical reactivity in smectic and cholesteric liquid crystalsJournal of the American Chemical Society, 1988