Chiral anchor groups for oxoanions: Asymmetric synthesis of tetrasubstituted bicyclic guanidines
- 13 June 1991
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 1991 (6) , 539-543
- https://doi.org/10.1002/jlac.199119910199
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Abiotic anion receptor functions. A facile and dependable access to chiral guanidinium anchor groupsThe Journal of Organic Chemistry, 1990
- Künstliche molekulare Anion‐Wirte. Die Synthese eines chiralen bicyclischen Guanidinium‐Salzes als funktionalisierte Ankergruppe für Oxo‐AnionenEuropean Journal of Inorganic Chemistry, 1990
- A novel synthesis of chiral guanidinium molecular hostsTetrahedron Letters, 1990
- Host‐Guest Bonding of Oxoanions to Guanidinium Anchor GroupsAngewandte Chemie International Edition in English, 1988
- Wirt‐Gast‐Bindung von Oxoanionen an Guanidinium‐AnkergruppenAngewandte Chemie, 1988
- Anion‐receptor molecules: Synthesis of a chiral and functionalized binding subunit, a bicyclic guanidinium group derived from L‐ or D‐ asparagineHelvetica Chimica Acta, 1988
- Tetazac: a novel artificial receptor for binding .omega.-amino carboxylatesThe Journal of Organic Chemistry, 1986
- Probing the design of a novel ditopic anion receptorJournal of the American Chemical Society, 1986
- Synthesis of an abiotic ditopic receptor moleculeTetrahedron Letters, 1984
- Synthese symmetrisch substituierter bicyclischer GuanidineEuropean Journal of Inorganic Chemistry, 1980