Chirality directed self-assembly. Resolution of 2,5-diazabicyclo[2.2.2]octane-3,6-dione and crystal structures of its racemic and (-) enantiomeric forms

Tetrahedron Letters

Volumn 35, Issue 44, 1994, Pages 8157-8160

  Brienne, Marie Josèphe ^a   Gabard, Jacqueline ^a   Leclercq, Martine ^a   Lehn, Jean Marie ^a   Cesario, Michèle ^b   Pascard, Claudine ^b   Chevé, Michel ^c   Dutruc Rosset, Gilles ^c  

^a l'alimentation et l'Environnement   (France)

^b CNRS   (France)

^c SANOFI   (France)

Author keywords

[No Author keywords available]

Indexed keywords

2,5 DIAZABICYCLO[2.2.2]OCTANE DERIVATIVE; BICYCLO[2.2.2]OCTANE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CRYSTALLOGRAPHY; DRUG PURIFICATION; ENANTIOMER;

EID: 0027945669     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(94)88270-3     Document Type: Article

References (14)

1. Perspectives in Supramolecular Chemistry—From Molecular Recognition towards Molecular Information Processing and Self-Organization
2. Supramolecular chemistry - Molecular information and the design of supramolecular materials
3. Molecular self-assembly and nanochemistry: a chemical strategy for the synthesis of nanostructures
4. The preparation of 2,5-diazabicycio[2.2.2] octane: A bridged piperazine
5. Antifilarial agents. Diazabicyclooctanes and diazabicycloheptanes as bridged analogs of diethylcarbamazine
6. Amino acids derivatives that stabilize secondary structures of polypeptides--
7. Oxidative removal of N-(4-methoxybenzyl) group on 2,5-piperazinediones with cerium(IV) diammonium nitrate.