3,7-Diazabicyclo[3.3.0]octane-2,6-diones: synthesis, NMR spectra and structures
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference10 articles.
1. 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
2. Synthesis of Chiral Bicyclic Bis-lactam Components for the controlled self-assembly of hydrogen-bonded arrays
3. α,α’-Diamino-α,α’-dicarboxyadipic acid tetraester: synthesis, lactamisation and dilactam structure
4. Chiral glycouril, 2,6-diethyl-2,4,6,8-tetraazabicyclo[3.3.0]octane-3,7-dione: spontaneous resolution, reactivity and absolute configuration
5. A synthesis of 3,7,10-triazatricyclo[3.3.3.01,5]undecane, ‘3,7,10-triaza[3.3.3]propellane’, and some derivatives
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1. ChemInform Abstract: 3,7-Diazabicyclo[3.3.0]octane-2,6-diones: Synthesis, NMR Spectra and Structures.;ChemInform;2010-06-13
2. Planar Chiral Dianthranilide and Dithiodianthranilide Molecules: Optical Resolution, Chiroptical Spectra, and Molecular Self-Assembly;The Journal of Organic Chemistry;2004-01-20
3. Competitive H-bonding in bicyclic bis-lactams: self-assembly in nanotubes or in unbalanced chiral threefold interpenetrated diamondoid network;Tetrahedron: Asymmetry;2002-12
4. 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
5. Directed synthesis of compounds capable to spontaneous resolution;Mendeleev Communications;2002-01
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