2,5-Diazabicyclo[2.2.2]octane-3,6-dione-1,4-dicarboxylic acids: synthesis, resolution, absolute configuration and crystal structures of the racemic and (–)-enantiomeric forms
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference13 articles.
1. Supramolecular Chemistry;Lehn,1995
2. 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
3. Synthesis of Chiral Bicyclic Bis-lactam Components for the controlled self-assembly of hydrogen-bonded arrays
4. α,α’-Diamino-α,α’-dicarboxyadipic acid tetraester: synthesis, lactamisation and dilactam structure
5. 3,7-Diazabicyclo[3.3.0]octane-2,6-diones: synthesis, NMR spectra and structures
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1. Molecular Solids from Symmetrical Bis(piperazine-2,5-diones) with Open- and Closed-Monomer Conformations;Crystal Growth & Design;2009-04-01
2. Planar Chiral Dianthranilide and Dithiodianthranilide Molecules: Optical Resolution, Chiroptical Spectra, and Molecular Self-Assembly;The Journal of Organic Chemistry;2004-01-20
3. Crystal engineering strategies in alkane-bis(ammonium) 2,5-diaza-3,6-dioxobicyclo[2.2.2]octane-1,4-dicarboxylates;Mendeleev Communications;2004-01
4. Competitive H-bonding in bicyclic bis-lactams: self-assembly in nanotubes or in unbalanced chiral threefold interpenetrated diamondoid network;Tetrahedron: Asymmetry;2002-12
5. Self-assembly of cage structures. Paper 12: The synthesis and crystal structures of 2,5-diazabicyclo[2.2.2]octane-3,6-dione-1,4-dicarboxylic acids and their diesters;Tetrahedron;2002-10
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