Electrophilic Substitution of Dibromoparacyclophane: A Route to Novel Paracyclophane Phosphine Ligands
Author:
Affiliation:
1. Johnson Matthey Catalysis and Chiral Technologies, Unit 28, Cambridge Science Park, Milton Road, Cambridge CB4 0FP, UK
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol049509f
Reference17 articles.
1. [2.2]Paracyclophane derivatives in asymmetric catalysis
2. Macro rings. XXXV. Transannular directive influences in electrophilic substitution of monosubstituted[2.2]paracyclophanes
3. Macro rings. XXXVI. Ring expansion, racemization, and isomer interconversions in the [2.2]paracyclophane system through a diradical intermediate
4. Macro rings. XXXVII. Multiple electrophilic substitution reactions of [2.2]paracyclophanes and interconversions of polysubstituted derivatives
5. A New Planar Chiral Bisphosphine Ligand for Asymmetric Catalysis: Highly Enantioselective Hydrogenations under Mild Conditions
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2. Kinetic resolution of substituted amido[2.2]paracyclophanes via asymmetric electrophilic amination;Nature Communications;2023-08-28
3. Regioselective Synthesis of 4,7,12,15‐Tetrasubstituted [2.2]Paracyclophanes: A Modular Route Involving Optical Resolution;European Journal of Organic Chemistry;2021-09-09
4. Enantiopure planar chiral [2.2]paracyclophanes: Synthesis and applications in asymmetric organocatalysis;Chirality;2021-07-24
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