A preparative microwave method for the isomerisation of 4,16-dibromo[2.2]paracyclophane into 4,12-dibromo[2.2]paracyclophane
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. A New Planar Chiral Bisphosphine Ligand for Asymmetric Catalysis: Highly Enantioselective Hydrogenations under Mild Conditions
2. Kinetic Resolution of rac-4,12-Dibromo[2.2]paracyclophane in a Palladium [2.2]PHANEPHOS Catalyzed Amination
3. [2.2]PHANEPHOS-Ruthenium(II) complexes: Highly active asymmetric catalysts for the hydrogenation of β-ketoesters
4. A Catalyst for Efficient and Highly Enantioselective Hydrogenation of Aromatic, Heteroaromatic, and α,β-Unsaturated Ketones
5. The First Structural Characterization of a [2.2]PHANEPHOS−Transition-Metal Complex: Structure of rac-[Pd(4,12-bis(diphenylphosphino)[2.2]paracyclophane)Cl2]
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1. [2.2]Paracyclophanes: From Selective Functionalization to Optical Properties;Advanced Optical Materials;2024-05-03
2. Microwave-assisted Organo-catalyzed C-C and C-X (Heteroatom) Bondforming Reactions: An Overview;Current Microwave Chemistry;2021-12
3. Metal‐to‐Metal Distance Modulated Au(I)/Ru(II) Cyclophanyl Complexes: Cooperative Effects in Photoredox Catalysis;Chemistry – A European Journal;2021-10-28
4. The Synthesis of Pyridyl[2.2]paracyclophanes by Palladium‐Catalyzed Cross‐Coupling of Pyridine Sulfinates;Advanced Synthesis & Catalysis;2020-12-21
5. Regioselective Functionalization of [2.2]Paracyclophanes: Recent Synthetic Progress and Perspectives;Angewandte Chemie International Edition;2020-02-03
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