The synthesis of enantiomerically pure [2.2]paracyclophane derivatives
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2008/OB/B800698A
Reference65 articles.
1. Comparison of the reactivity of [2.2]paracyclophane and p-xylene
2. Planar and Central Chiral [2.2]Paracyclophanes as Powerful Catalysts for Asymmetric 1,2-Addition Reactions
3. Macro Rings. I. Preparation and Spectra of the Paracyclophanes
4. Preparation and Structure of Di-p-Xylylene
5. Cycloadditions of α-(4-[2.2]paracyclophanyl)-N-methyl nitrone
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1. Synthesis and characterization of one-handed helical oligo(o-phenylene)s: control of axial chirality by planar chiral [2.2]paracyclophane;Chemical Communications;2024
2. Aggregation-induced emission from optically active X-shaped molecules based on planar chiral [2.2]paracyclophane;Scientific Reports;2023-12-19
3. Optically Active A‐Shaped Cyclic Molecules Based on Planar Chiral [2.2]Paracyclophanes Emitting Bright Circularly Polarized Luminescence with High Anisotropy Factors;Advanced Functional Materials;2023-10-29
4. Kinetic resolution of substituted amido[2.2]paracyclophanes via asymmetric electrophilic amination;Nature Communications;2023-08-28
5. Correlation Between Orientation of the Stacked π‐Electron Systems and Chiroptical Properties;ChemistrySelect;2023-07-13
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