(3+3)-Cyclocondensation of the enantiopure and racemic forms of trans-1,2-diaminocyclohexane with terephthaldehyde. Formation of diastereomeric molecular triangles and their stereoselective solid-state stacking into microporous chiral columns-Reference-Cited by-同舟云学术

(3+3)-Cyclocondensation of the enantiopure and racemic forms of trans-1,2-diaminocyclohexane with terephthaldehyde. Formation of diastereomeric molecular triangles and their stereoselective solid-state stacking into microporous chiral columns

Published:2001-02 Issue:1 Volume:12 Page:127-133
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Chadim Martin,Buděšı́nský Miloš,Hodačová Jana,Závada Jiřı́,Junk Peter C.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference12 articles.

1. The Quest For Extra-Large Pore, Crystalline Molecular Sieves

2. From Disymmetric Molecules to Chiral Polymers: A New Twist for Supramolecular Synthesis?

3. Self-Assembly of 1,1′-Biphenyl-2,2′,6,6′-tetracarboxylic Acid: Formation of an Achiral Grid with Chiral Compartments

4. Self-assembly of enantiopure 2,2′-dimethylbiphenyl-6,6′-dicarboxylic acid. Formation of chiral squares and their columnar stacking

5. Directed Self-Assembly of Chiral, Optically Active Macrocyclic Tetranuclear Molecular Squares

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